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دراسة التاثير المخفض - المضاد لفرط سكرالدم للمركبات الكيميائية الفعالة المعزولة من النبات الطبي العراقي شوك البحر == Study of Hypoglycemic Antihyperglycemic Action of Active Chemical Compounds Isolated from Iraqi Prosopis juliflora Medicinal Plant

Author name: جمال حربي حسين السعدي
Supervisor name: عباس دواس مطر المالكي
General topic: Chemistry
Specific topic: Analytical Biochemistry
Degree: Doctorate
Language: English
University location: Basrah
First pages:
Abstract: Diabetes mellitus is a disorder in glucose sugar metabolism process becauseof different reasons.leading to a great damage in body systems , therefore medicinalplants were used successfully to treat this disease .The current study was carried outIraqi prosopis juliflora to determine and investigate its hypoglycemic action in bloodof normalglycemic and alloxan induced hypoglycemic rabbits. Many generalextracts were prepared from Iraqi prosopis juliflora pod and leaves ,they are hotaqueous ,cold aqueous ,hot alcoholic ,cold alcoholic ,oils, ethyl acetate and dichloromethane extract .Moreover , some chemical families were isolated from this plantsuch as phenols ,glycosides , flavonoids , tannins ,alkaloids and saponnins.Preliminary qualitative tests were carried out for all prepared extracts thenhypoglycemic and fasted alloxan - induced hyperglycemic rabbits to know activitythese extracts in decreasing blood glucose levels in these rabbits . the resultsindicated that all extracts showed good decreasing in glucose level. Oil extractisolated from prosopis juliflora leaves showed very high activity to decrease blood glucose ,levels in normalglycemic and hyperglycemic rabbits ,where significant decreasing (P<0.05) was found at second and forth hrs , significant decreasing (P<0.01) at sixth hr. and high significant decreasing (P<0.001) at twenty forth hrs. ,whereas leaves glycosides has a great ability to decrease glucose levels in normalglycemic rabbits where a significant decreasing (P<0.01) was found at second and forth hrs., and a high significant decreasing (P<0.001) at twenty forth hrs., but in hyperglycemic abbits , a high activity was recorded and led to a significant decreasing ( P<0.01) at second forth hrs., and high significant lowering( P<0.001 ) at twenty forth .whereas ,leaves tannins extract was noticed to be the lowest affiecieney in reducing blood glucose levels ere it led to a significant lowering ( P<0.01) at twenty forth in normalglycemic rabbits , while a significant decreasing (P<0.05) was recorded at twenty forth in hyperglycaemic rabbits. Leaves ,4 - (2’ - Hydroxyethyl)phenol, Trans - phytol , 24 - Methylencycloartan - 3 - one β - hydroxylup - 20(29) - en 4 - (β - D - Glucopyranosyloxy)benzyl alcohol and Sti masterin (.Were isolated ,separated ,purified and identified by thin layer chromatography, column chromatography, gas chromatography, IR - spectroscopy ,1H,C13 - NMR ,Gas chromatography - mass spectroscopy .Also study of hypoglycemic action of four these chemical compounds isolated from leaves and pods p.juliflora , the glycosidic compound 4 - (β - D - Glucopyranosyloxy)benzyl alcohol recorded strong activity as hyperglycemic action and led to a significant decreasing ( P<0.05) at second hrs., and significant lowering( P<0.01)at fourth ,sixth hrs. and high significant decline (P<0.001) at 24 hrs in normalglycemic rabbits ,while in hyperglycemic rabbits a significant decreasing (P<0.05) at second hrs. ,significant lowering P<0.01 at fourth and sixth hrs and significant decreasing (P<0.001) at twenty forth hrs. The active compound 4 - (2 - - Hydroxyethyl)phenol showed a high hypoglycemic action were significant decline ( P<0.05) at second hrs, a significant decreasing ( P<0.01) at sixth and a high significant decreasing (P<0.001) at twenty forth hrs. in normalglycaemic rabbits ,while in hyperglycemic rabbits , a significant decline (P<0.05) was at second , a significant decreasing (P<0.01) at fourth and sixth hrs., and a high significant decreasing ( P<0.001) was recorded at twenty forth hrs..Also active compound24 - Methylencycloartan - 3 - one showed a significant decrease (P<0.05) at second hrs. , significant decrease (P<0.01) at fourth and sixth hrs., and a high significant decreasing ( P<0.001) at twenty forth hrs hyperglycaemic rabbits, while the compound α - tocopherol recorded a significant decreasing (P<0.05) at sixth hrs. , significant decrease (P<0.01) at twenty forth hrs. in hyperglycemic rabbits. The toxicity for some extracts and active chemical compounds isolated from leaves and pods was studied where no hemolytic for red blood cells was found .

تحضير ودراسة تحليلية - طيفية لبعض اصباغ الازو غير المتجانسة واستخدام احدها في استخلاص النحاس الثنائي من المحاليل المائية == Preparation and Analytical Study of Some Heterogeneous Azo Dyes and Using One of Them in Extraction of Cu(II) From Aqueous Solutions

Author name: لمياء عبد اللطيف رسن
Supervisor name: اسعد عبود علي
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: Arabic
University location: Basrah
First pages:
Abstract: The thesis involves three parts : The first part included synthesis eight new Azo dyes,derived of Procaine and Metoclpramide : LR1R = 3 - [ ( Procaine ) azo ] - 2 - hydroxyl indoleLR2R = 2 - [ ( Procaine ) azo ] - 4,5 - diphenyl ImidazolLR3R = 2 - [ ( Procaine ) azo ] - 3 - PhenylephrineLR4R = 2 - [ ( Procaine ) azo ] Imidazol, L5 = 2 - [ ( Metoclopramide ) azo ] Imidazol,LR6R = 2 - [ ( Metocopramide ) azo ] 3 - PhenylephrineLR7R = 3 - [( Metoclopramide ) azo ] 2 - hydroxyl indoleLR8R= 2 - [( Metoclopramide ) azo ] - 4,5 - diphenyl ImidazolThey have been described by C.H.N. and Visible spectroscopic spectra and the functional groups were characterized by I.R technique like azo group of (1558.48 , 1512.19 ,1581.63 , 1508.12 , 1521.84 , 1529.55 , 1517.98 , 1533.14 ) cm - P 1 P for azo dyes (LR1R LR2R , LR3R , LR4R , LR5R , LR6R , LR7R , LR8R) respectively The Acid - Base properties were also studied spectrophotometric using buffer solutions of pH values of (0.67 - 12) in the visible region, From the spectra obtained the protonation an ionization constants of azo dyes were determined by using Half - Height method ,the isopiestic point were also established ,which indicated the suggested mechanism for the ionization and protonation steps.The effect of solvents of different polarities was also studied on the spectra shift in the visible region. It was found that linearity relation between the dielectric constants of solvents and λRmaxR this denotes the dielectric constants at the mediumis the main factor governing the band shift, except for (LR6R) azo dye which give little deviation from linearity . The second part concerns with the ability of azo dye (LR8R) for forming complex with Cu(II) , The optimum conditions for forming stable azo dye - complex were studied like pH effect , kind of buffer solution , time effect and sequence of addition of reagents by aid molar ratios method and Continuous variation method It was found that stable complex was obtained with stoichiometry of 1 : 2 ( M : L ) From calibration curve of (L8) complex , : Sandell sensitivity 2.492× 10 - 3 μg cm - 2, Detection limit 0.00977 μg ml - 1, Standard deviation 0.00193, Correlation coefficient 0.994 , molar absorbitivity coefficient 2.547×104 L mol - 1cm - 1 , specific absorbtivity 0.4012 ml g - 1cm - 1 and obeyness of Beer's law linearity up to 3.20 ppm The effect the interference of some important cations and anions of concentration (1 - fold, 5 - fold and 10 - fold ), the stability of this complex was showed through determination of their conformation constants (stability constants) by use the corresponding solution method ,by aid of using half value method .this complex had been characterized by (FT - IR) according to the different of shift relativity abundance of same active groups bundle complex comparison with privately dyes ; the azo group ( - N=N - ) and (C=N) groups.,the percentage to metal (Cu) in the complex determine by using of result Atomic Absorption Spectroscopy where found approximate the same between theoretical and measurement.The third part : involved solvent extraction of Copper(II) ions from its aqueous solution by using L8 to organic solution. This study include limitation of optimum conditions for complex formation of highest observed absorbance of λmax at complex : such as (pHex=7) ,ions concentration Copper(II) 15μg effect shaking time of two immiscible phase 15 min .the distribution ratio (D*).and extraction percentage (%E) were determination.Organic solvent effect study appeared there is not any linear relation between dielectric constant (D) of organic solvents and distribution ratio (D*) that’s mean there is not any effect for polarity of organic solvent on extraction method but there is an effect for organic solvent structure which is participate in the structure of ion pair complex extracted by formation tight ion pair or loose ion pair as well experiment result illustrate chloroform organic solvent it was the best organic solvent in extraction .Thermodynamic study include Temperature effect on extraction efficiency the experimental results demonstrate the reaction was exothermic for Copper(II) with organic reagent (LR8R) endothermic reaction , after calculation thermodynamic data ΔHRexR , ΔGRexR , ΔSRex Rshow entropy values was high that is mean complexion reaction is entropic in region

تحضير ايمايدات حلقية ثنائية وبعض مشتقاتها الكبريتية ودراسة خواصها الطيفية والتركيبية , عمليا ونظريا باستخدام نظرية دالية الكثافة == IR, NMR, MS Spectra and Structure of Some prepared Bicyclic Imides and Their Thione Derivatives; Experimental and Density Functional Theory studies

Author name: عادل امعلا ضمد ال ازيرج
Supervisor name: ناجي علي عبود
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: English
University location: Basrah
First pages:
Abstract: The present work involved four parts : First step concerned with the preparation some N, N’ - alkyl (aryl) bismaleimic acidsvia reaction of twice molar amounts of maleic anhydride and hydrazine for compound(A1), and different alkyl and aryl - diamines for compounds A2 - A7. The reaction wascarried out via nucleophilic attack of amino group in maleic anhydride. The structureof the compound (2Z,2Z’) - 4,4’ - (ethane - 1,2 - diylbis (azanediyl)) bis (4 - oxobut - 2 - enoicacid) (A2) was also unambiguously confirmed by X - ray single crystal structureanalysis. The white crystal crystallizes in the monoclinic system, space group C2/cwith the cell dimensions a =7.108(3), b=7.370(2), c= 20.859(6) Å, β = 91.260(4)oand Volume = 1092.65(6) Å3.Molecule is stabilized by an intramolecular O—H…O hydrogen bond. In thecrystal, molecules are connected through intermolecular N—H…O hydrogen bonds.Intermolecular and intramolecular hydrogen bonds coexist to stabilize the structure.The geometry calculated of compounds A1 - A7 was optimized using a Densityfunctional theory DFT with B3LYP hybrid functional and 6 - 311G (d, p) basis set, andis in good agreement with the structure obtained by the X - ray single crystal structureof compound A2. Also the fundamental vibrational frequencies of vibrational bandswere evaluated.The second part of this study was the treatment of N,N - alkyl and (aryl)bismaleimic acid (A1 - A7) with suitable dehydrating agents lead to dehydration andcyclization producing the corresponding N,N - alkyl and (aryl) bismaleimide (AD1 - AD7).The structure of the compound 1,1’ - (sulfonylbis(4,1 - phenylene)) bis (1H - pyrrole - 2,5 - dithione) (AD7) was also unambiguously confirmed by X - ray single crystalstructure analysis. The colorless crystal crystallizes in the monoclinic system, spaceAbstractix0200040000CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2phenyl4,4' - sulfonyldianilinedirect Aliphatic AromaticWavenumber cm¯¹Types of RCH str.CH2 - N strC=O strC - Ngroup P21/c with the cell dimension a =11.698(3), b=15.002(3), c= 20.053(6)Å andβ = 98.818(2)o Volume = 3478.07(13) Å3.FT - IR spectra show the position of the absorption bands vary with the type andlength of the link spacer (R) between the two maleimide rings on the compoundsAD1 - AD7.The absorption frequency of vinyl group increases with increasing methylene aliphatic chain spacer link between two maleimides ring, the correlation between some absorption bands and the type (direct link or aliphatic or aromatic) and length of aliphatic chain link spacer (R) between the two maleimide rings in the studied compounds AD1 - AD7 shown in the chart below.In the third part, a series of new bisthimalemide derivatives were prepared by thionation the compounds AD3, AD6 and AD7 with Lawesson’s reagent LR. Subsequent reaction of bismaleimimides AD3, AD6 and AD7 with Lawesson’s reagent afforded dithio derivatives.

دراسة حيوية كيميائية لتاثير بعض المعادن الثقيلة على حالة الاكسدة مضادات الاكسدة في عمال محطات البنزين في محافظة البصرة العراق == Biochemical Study of the Effects of Some Heavy Metals on Oxidant / Antioxidant Status in Gasoline Station Workers /Basra - Iraq

Author name: سنان كاظم شنان
General topic: Chemistry
Specific topic: Analytical Biochemistry
Degree: Doctorate
Language: English
University location: Basrah
First pages:
Abstract: Emission of gasoline and its combustion products are consideredmajor air pollutants with adverse effects on the antioxidant systems in thehuman. The effects of exposure to the vapors of motor gasoline (vehiclesfuel in Basrah), on workers were investigated. The current study included50 workers exposure to gasoline in the gasoline filling stations, ranging inage from 18 to 56 years at a mean of (30.45 ± 9.31), in addition to thecontrol group, which consisted of 50 healthy individuals (non - workingstations filling) ranging in age from 18 to 50 years at a mean of (30.27 ±10.37).The study aims to find a number of biochemical indications and theirrelationship with exposure to gasoline by estimating the activity of the enzyme (δ - aminolaevuIinate dehydratase (ALAD)) which is considered as an indicator of the extent of poisoning by heavy metals, study the activity of enzymatic antioxidant (Glutathione peroxidase (GPx), Superoxide dismutase (SOD), Glutathione reductase (GRx), Glutathione S - transferase (GST), Catalase (CAT)), non - enzymatic antioxidants glutathione reduce glutathione (GSH), study the level of Malondialdehyde (MAD), Total antioxidant capacity (TAC), trace elements (Selenium (Se), Znic (Zn), Copper (Cu), magnesium (Mg)) and heavy metals (lead (pb), mercury (Hg), Cadmium (Cd)) and the results were as follows : 1 - Highly significant decreasing (p <0.001) in workers in the levels of trace elements (Se, Cu, Zn) compared with healthy control, while significantly decreased (p <0.05) in the level of Mg with high significantly increased in the levels of heavy metals (Pb, Hg and Cd) (p <0.001). On the other hand, The results indicated that trace elements (Cu, Mg, Zn, Se) were decreased with increasing of the period of gasoline station workers while for heavy metals (Pb, Hg, Cd) increased were observed.2 - The level of MAD, the end product of lipid peroxidation, was high significantly elevated (P<0.01) contact with a significant decreasing (p <0.05) in the level of TAC in workers when compared with healthy controls. MDA increased with the increase of the period of gasoline station workers. MDA concentrations were increased significantly, indicating the amount of cellular damage. Increase the level of MDA from pollution as the period of pollution, increased might decrease TAC in workers compared with healthy control.3 - Workers group showed a highly significant decrease in the activity of enzymes (SOD, CAT, GPx, GRx, GST, ALAD) and level of GSH (p<0.001) compared with healthy controls. The results showed that increasing the duration of the work in the filling station to produceadecrease in the activity of the enzymes (SOD, CAT, GPx, GRx, GST, ALAD) and level GSH. Also, the current study include the assessment of the impact of heavy metals and MDA on the levels of trace elements (Cu, Mg, Zn, Se), (GSH, TAC) and the activity of the enzymes (SOD, CAT, GPx, GRx, GST, ALAD) through the study of the correlation coefficient (p) and the results were as follows : 1 - The level of MDA showed a highly significant negative correlation with the activity of enzymes SOD (P<0.001) and (GRx, ALAD with p<0.01), a highly significant positive correlation with levels of heavy metals (Pb, Hg, Cd), a significant negative correlation (p<0.05) with levels of (Se, Zn, Mg, GSH) and activity of enzymes (CAT, GRx) and a negative correlation with no significant (P>0.05) with level of Cu and activity of GST in workers.2 - The level of Pb shows a highly significant negative correlation with the levels of trace elements Cu, Zn, Se and activity of enzymes GRx, ALAD (P <0.01), while (p <0.001) with the level of TAC, GSH and activity of enzyme GST, GPx, SOD, a significant negative correlation with level of CAT (P <0.05) and a negatively correlated with no significant with the level of Mg in workers of gasoline stations.3 - The study illustrate also a highly significant negative correlation between Hg level and levels of (Zn, Mg, Cu, TAC) and SOD activity (P < 0.001), while there was a significant negative correlation (P < 0.05) with the level of Se and CAT, GPx, GRx, ALAD activity and a negative correlation, but not significantly with level of GSH and GST activity in serum of gasoline station workers.4 - The level of Cd showed similar behavior of other heavy metals a highly significant inverse correlation with the levels of Se, Cu, TAC and the activity of SOD (p <0.001), a significantly with the level of Zn, GSH and ALAD, CAT, GPx activity (p<0.05), while there was a negative correlation , but not significant (P > 0.05) with levels of Mg and GRx , GST activity in workers.

تحضير وتشخيص بعض البوليمرات لازالة بعض ايونات العناصر والبنتونايت من مياه الفضلات == SYNTHESIS AND CHARACTARIZATION OF SOME POLYMERS FOR THE REMOVAL OF SOME HEAVY METAL IONS AND BENTONITE IN WASTE WATERS

Author name: حسن ثامر عبد الصاحب ذياب
Supervisor name: عبد الامير حسين تعوبي | صلاح شاكر هاشم
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: Arabic
University location: Basrah
First pages:
Abstract: تضمنت الدراسة الحالية عزل بعض المركبات البوليمرية الطبيعية وهي : الكيتوسان,اللكنين والتانين من مصادر طبيعية وهي قشور الروبيان , السائل الاسود وورق الغار على التوالي , ومن ثم تحضير ثلاث بوليمرات متشابكة منها باستخدام البيوترالديهايد كعامل تشابك والبوليمرات المحضرة هي : الكيتوسان المتشابك مع اللكنين : P1 الكيتوسان المتشابك مع التانين : P2 التانين المتشابك مع اللكنين : P3 تم تشخيص البوليمرات المعزولة والبوليمرات المحضرة بواسطة تقنيات : الاشعة تحت الحمراء , مطيافية الكتلة - كروماتوغرافيا الغاز , الاشعة السينية اضافة الى التحليل الوزني الحراري لتحديد تركيب البوليمرات ومن ثم دراسة التطبيقات التحليلية لها والتي قسمت الى قسمين رئيسين هما : 1 - ازالة الايونات الفلزية : شملت هذه التطبيق دراسة تاثير كمية البوليمر , الاس الهيدروجيني . زمن المزج لاجل تحديد الظروف المثلى لازالة بعض ايونات العناصر الثقيلة ثنائية التكافؤ : الكادميوم , الكوبلت , الرصاص والزنك من المحاليل المائية حيث اظهرت التجارب ان الايونات الفلزية ازيلت بكفاءة عالية عند دالة حامضية تساوي 8 لجميع البوليمرات المدروسة . واظهرت نسبة واطئة من انتفاخ البوليمر وان هاتين الخاصيتين اساسيتين للبوليمر والذي بالامكان استخدامه كرا تنج لازالة الايونات . كذلك بينت الدراسة الحالية ان العدد الكبير من مجاميع الهيدروكسيل ومجاميع الامين على البوليمرات المحضرة (P1 ,P2 ,P3) اظهرت كفاءة امتزاز اعلى من الكيتوسان واللكنين والتانين بذاتها لذلك من الواضح ان جميع البوليمرات المحضرة اظهرت كفاءة عالية وانها بالامكان استخدامها مرة اخرى بعد اعادة تنشيطها باستخدام حامض الهيدروكلوريك ذو تركيز (3 عياري) خصوصا (P1 ,P2 ,P3) والتي اظهرت كفاءة ازالة عالية للايونات اعلى من 99% باستخدام اقل كمية من البوليمر واقل زمن (2,5 ساعة) وسهولة الترشيح عما في حالة استخدام الكيتوسان واللكنين والتانين.2 - التخثر والنزول : هدفت هذه الدراسة الى بحث تطبيق البوليمرات العضوية المعزولة والمحضرة والحاوية على مجاميع الهيدروكسيل ومجاميع الامين . حيث استخدمت هذه البوليمرات كمخثرات لازالة تعكرية اطيان البنتونايت من المياه ويعود ذلك الى وجود مجاميع الهيدروكسيل ومجاميع الامين الفعالة في تركيبها . بينت الدراسة الحالية ان المعاملة الكافية للمياه تتطلب عناية خاصة . اجري كشف الجار واختبرت كفاءة هذه البوليمرات لازالة تعكرية اطيان البنتونايت تحت ظروف مختلفة وهي : كمية البوليمر , الاس الهيدروجيني , سرعة المزج اضافة الى زمن النزول. وكذلك تم استخدام نوعين من المياه : مياه خام ومياه محضرة لايجاد ميكانيكية ازالة اطيان البنتونايت والعلاقة بين الازالة وخصائص البوليمر. بينت الدراسة ان استخدام البوليمرات المتشابكة (P1 ,P2 ,P3) لازالة اطيان البنتونايت يؤدي الى ازالة بكفاءة عالية جدا اعلى من 99% وذلك لان كفاءة الازالة ليست فقط ناتجة من اختزال البنتونايت الموجودة في الماء الى ادنى مستوى ولكن ايضا في انتاج حجم اطيان واطئ النسبة اقل من 10% من حجم الماء .كذلك ان استخدام البوليمرات المتشابكة سوف يقلل كمية المخثر المستخدم الى اقل من النصف وكذلك يقلل كلفة المخثرات الكيمياوية الى الثلث. وعموما ان استخدام المخثرات (P1 ,P2 ,P3) يؤدي الى تنزيل الاطيان بشكل اسهل واقوى واكبر من الكيتوسان , اللكنين , التانين بذاتها. حيث اظهرت البوليمرات المحضرة (P1 ,P2 ,P3) كفاءة امتزاز ممتازة بلغت 99,8% , 99,6% , 99,8% عند الظروف المثلى. ان الطريقة الفيزيو - كيميائية المستخدمة في الدراسة الحالية لمعاملة المياه تتمثل بصورة رئيسية بالبساطة ,السهولة , الكلفة الواطئة , اضافة الى كفاءة الازالة الممتازة.كذلك ان استخدام المعاملة الفيزيو كيميائية ينتج مياه بنوعية جيدة.

تحضير ودراسة الفعالية البايلوجية لبعض مركبات 4 - ثايازوليدينون المشتقة من 1, 4 - ثنائي هايدروبريدين الجديدة == Synthesis and Biological ActivityStudy of Some new 4 - Thiazolidinone compounds Derivatives From 1, 4 - Dhydropyridine

Author name: تحسين صدام فندي المذخوري
Supervisor name: تحسين عبد القادر
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: Arabic
University location: Basrah
First pages:
Abstract: تضمنت الدراسة تحضير بعض مركبات الثايازوليدينون المشتقة من ثنائي هايدروبريدين في خمس خطوات الخطوة الاولى : تحضير ثنائي هايدروبريدين (TA1) من مفاعلة بارا هايدروكسي بنزلديهايد مع مولين من الايثل اسيتو اسيتيت وهيدروكسدالامونيوم في الايثانول كمذيب في خطوة واحدة كما في المعادلة الخطوة الثانية : تحضير المركب (TA2) من تفاعل المركب (TA1) مع كلورو ايثايل اسيتيت بوجود كاربونات البوتاسيوم في DMF كمذيب كما في المعادلة الخطوة الثالثة : تحضير DHPs - hydrazide (TA3) من تفاعل الهيدرازين مع المركب (TA2) في الايثانول كما في المعادلة الخطوة الرابعة : تحضير مركبات الهايدروزونات (TA4 - TA15 ) من تفاعل المركب (TA3) مع عدد من الالديهايدات الاروماتيه باضافة قطرتين من حامض الخليك الثلجي كعامل مساعد في الايثانول كما في المعادلة الخطوة الخامسة : تحضير مركبات الثايازوليدينون (TA4a,TA6a - TA15a) من تفاعل المركبتو حامض الخليك مع مركبات الهايدروزوناتالمحضرة في الخطوة السابقة وباستخدام كلوريد الخارصين ZnCl2كعامل مساعدفي DMFكما في المعادلة شخصت المركبات المحضرهبالطرق الطيفيه مثل تقنية الاشعه تحت الحمراء FTIR وتقنية الرنين المغناطيسي للهيدروجين والكاربون والنتروجين 1H - NMR و13C - NMR و15N - NMR وDEPT - 135 - 13C - NMRبالاضافة الى اطياف الكتله تقنيةESI.تميز طيف IR للمركب TA1 بظهور حزمة عريضه عند cm - 13500 - 3150 واخرى عند 1660cm - 1تعود للتذبذب الاتساعي لمجموعتيOH/NH المتداخله وكاربونيل الاستر على التواليكما بين طيف 1H - NMR اشارات احايه عند الازاحه الكميائيه 9.09ppmδ وδ8.70ppm تعود لرنين بروتون مجموعةOH الفينوليهوبرتون NH العائد لحلقة DHP على التوالي وفي المركب TA2تظهر حزمتيننتيجه للتذبذب الاتساعي لمجموعتي الكاربونيل الاستريه عند العدد الموجي 11743cm - و1691cm - 1واظهر طيف 1H - NMR للمركب TA2اشارتين جديدتينالاولى متعدده نتيجه لرنين بروتوني OCH2 والثانية ثلاثية تعود الى رنين بروتونات CH3 للممجموعة الاستريه OCH2CH3 - عند الازاحه δ4.15ppm وδ1.20ppm وعلى التوالي كما بين طيف المركب TA2 ايضا اختفاء الاشارة العائده لرنين بروتونOH عند δ9.09ppm وظهور اشارة احاديه عند δ4.69ppm تعود لرنين بروتوني OCH2COمما يثبت ان مجموعة الهيدروكسيل الفينوليه هي التي عانت تفاعل اضافة وليس مجموعة الامينNH التابعة لحلقة DHP.واظهر طيف IRللمركب TA3تغير في التذبذب الاتساعي لمجموعة الكاربونيل من العددالموجي 1743cm - 1 الى عدد موجي اقل 1662cm - 1دليل على تكون المركب 3TA وفي طيف 1H - NMR للمركبTA3 فقد اظهر اشارتين احاديتين عند الازاحات الكيميائيه δ9.27ppmوδ4.30ppm نتيجة لرنين بروتونات NH وNH2 على التوالي. كما اظهر طيف IR لمركباتالهايدروزونات حزما لمجموعة الازوميثين الجديده عند العدد الموجي cm - 11612 - 1604دليل على تكون مركبات الهايدروزونات كما اظهرطيف1H - NMR للمركبات (TA4 - TA15)اشارة تعود لرنين بروتون مجموعة الازوميثين - N=CH - عند الازاحه الكميائيه δ(7.91 - 8.37)ppm مما يؤكد ذلك. اما بالنسبة لمركبات TA4a,TA6a - TA15a))فقد اظهرطيف IR عند 1718cm - 1 - 1672تعود الى التذبذب الاتساعي لمجموعة كاربونيل حلقة الثايازوليدينون الجديده دليل على تكون مركبات 4 - الثايازوليدينون المشتقة من ثنائي هايدروبريدينكما ان ظهور اشارات جديده في طيف 1H - NMR لمركبات(TA4a,TA6a - TA15a) منها اشارتين جديدتين نتيجه لرنين بروتون ( - SCHN - ) عند الازاحه δ(5.52 - 6.65) ppm وδ (5.16 - 5.67)ppm التي تدل على وجود ايزومرين فراغيين بالاضافه الى اشارات ثنائيه - ثنائيه اومتعدده نتيجه لرنين بروتونات( ( - CH2 - S عند الازاحه δ(4.60 - 3.54) وδ (3.51 - 3.89)ppm كل هذه الاطياف تؤكد صحة المركبات المحضرة بالاضافة الى اطياف13C - NMRوالكتله والتي استخدمت تقنية ESI - MS لدراسة اطياف الكتلة لمركبات الثايازوليدينون وقد اظهرت اطياف المركبات ذروه [M+H] دلالة على اتفاقها مع التراكيب المحتملة. كما اظهرت بعض المركبات TA11a ,TA4a, TA6, TA5 وTA15a فعالية تثبيطية اتجاة بكتريا E.coli وS. aureus , اما المركبات TA7a وTA8a وTA9aو TA12a وTA13a وTA14a لم تظهر فعالية تثبيطية اتجاة جنسي البكتريا S. aureus وبكتريا E.coli , وبينت الفحوصات المختبريه بان المركبات المحضره ذات سمية خلويهcellular toxicity واطئه جدا. | This study includes the preparation some of thiazolidinone compounds derivatives from dihydropyridine in five steps .1st step preparation of dihydropyridine (TA1) from the reaction of4 - hydroxybenzaldehyde with ethylacetoacetate and ammonia under reflux in ethanol . 2nd step preparation (TA2) compound from treated (TA1) with chloroethyl acetate being potassium carbonate (K2CO3) in DMF as a solvent. 3rd step preparedofDHPs - hydrazide (TA3) from(TA2) with hydrazine hydrate in ethanol under reflux.4th step preparation of hydrazonecompounds (TA4 - TA15) from reacted (TA3) with aromatic benzaldehyde dissolved in ethanol and presence acetic acid as a catalyst. 5th step preparation of (DHP - thiazolidin - 4 - one)(TA4a - TA15a) from convertedhydrazone compounds which are (TA4 - TA15) by treated with 2 - mercapto acetic acid in DMF and presence ZnCl2 as a catalyst.All the synthesized compounds were identified by IR, 1H - NMR ,13C - NMR , DEPT - 135 - 13C - NMR, 15N - NMR and mass spectra usingElectrospray Ionization technique.The IR spectral data of compound TA1showed strong band at3500 - 3150cm - 1 and 1660cm - 1due to stretching vibration NH/OHand ester groups, respectively.This was further confirmed by its 1H - NMR spectrum, where it displayed singlet signal at δ 9.09 and δ 8.70 ppm, which are attributed to phenolic OH and NH proton of DHP ring, respectively.The presence of two ester groups were confirmed by its IRshowed strong band at 1743cm - 1 and 1691cm - 1 due to carbonyl ester and amide respectively and 1H - NMR spectrum where in it showed multiple and triplet at δ4.15ppm and δ 1.15 ppm respectively for ester OCH2CH3 group. Appearance of a singlet at δ4.69ppm that corresponds to OCH2CO proton further confirms the proposed structure of the product.In 1H - NMR spectrum of compound TA2 disappearance of OH peak at δ 9.09 ppm clearly established that phenolic hydroxyl group was alkylated but not NH group of DHP ring.In FTIR spectrum of hydrazide TA3 shifting of carbonyl stretching frequency from 1743 cm - 1 to lower frequency 1662 cm - 1 indicated the formation of TA3. Further, its 1H - NMR spectrum displayed two singlet at δ 9.27 and δ 4.30 ppm confirming the presence of hydrazidic NH and NH2 groups. Formation of various hydrazones TA4 - TA15 from hydrazide TA3 was evidenced by their FTIR and 1H - NMR spectra. The IR spectra data of DHPs hydrazone derivatives (TA4 - TA15) showed strong band at1612 - 1604cm - 1 and 1H - NMR spectrumofTA4 - TA15showed a new peak at a singlet signal around δ (7.91 - 8.37)ppm corresponds to - N=CH - proton in the place of a singlet at δ 4.28 ppm confirming its structure.The heterocyclic system of 4 - thiazolidinone has been of compound TA4a, TA6a - TA8a, show two signal of proton - CH ( - SCHN - ) at δ(5.52 - 6.65)ppm and δ(5.16 - 5.67)ppm Corresponding to the two optical isomers form. As well as doublet of doublet or multiple signal around δ(4.60 - 3.54) ppm and δ (3.51 - 3.89)ppm attribute to methylene group( - CH2 - S).The 13C NMR and HRMS (ESI) confirms the proposal structural elucidation of DHPs thaiazolidin - 4 - one derivatives (TA4a, TA6a - TA8a), the ESI reveals the observe [M+H] is good agreement with calculate [M+H] , the biological activity of the synthesis compounds prepared as antibacterial agents as well as low cellular toxicity.

تحويـر المواصفات الريولوجيـة للاسفلـت بالمعالجـة مـع البولـي ستايريـن == Modification of Rheological Properties of Asphalt by Treatment with Polystyrene

Author name: ايمان اسماعيـل احمـد
Supervisor name: عماد عبد القادر فائق صالح الدبوني
General topic: Chemistry
Specific topic: Industrial Chemistry
Degree: Doctorate
Language: English
University location: Mosul
First pages:
Abstract: اكتسبت المواد الاسفلتية المحورة بالبوليمرات اهمية خاصة خلال السنوات الاخيرة وذلك لارتباطها الوثيق بالمجالات الانشائية والصناعية فضلا عن التغيرات الكبيرة الحاصلة في السلوك الريولوجي للمواد الاسفلتية عند اضافة كميات صغيرة من البوليمر.ونظرا لمحدودية عدد الدراسات حول استخدام البولي ستايرين لتحوير الاسفلت جاءت دراستنا هذه محاولة لتوضيح كيفية تصرف البولي ستايرين مع الاسفلت خصوصا اذا علمنا ما تتمتع به مادة البولي ستايرين من مميزات كونها واحدة من اكثر البوليمرات الثرموبلاستيكية شائعة الاستعمال ورخيصة الثمن بالاضافة الى حجم المشاكل البيئية الناجمة عن تراكم كميات كبيرة من هذه المادة كفضلات.اشتملت هذه الدراسة على : 1 - معالجة كل من اسفلت بيجي المشتق من نفط بارافيني الاساس واسفلت قيارة المشتق من نفط اروماتي الاساس بنسب مختلفة من البولي ستايرين معالجة اذابة فيزيائية، بالاضافة الى المعالجة الكيميائية لاسفلت بيجي مع البولي ستايرين.2 - معالجة اسفلت بيجي بنسب مختلفة من البولي ستايرين المكسر حراريا ، معالجة اذابة فيزيائية ، ومعالجة كيميائية ، وملاحظة تاثير تقليل الوزن الجزيئي للبوليمر على تجانسية الاسفلت.3 - تحضير انظمة اسفلتية بالمعالجة الكيميائية المحفزة مع الكبريت لكل من اسفلت بيجي والقيارة ومن ثم اجراء عمليات التحوير بالبولي ستايرين والهدف دراسة مقدار التمازج Compatibility بين البولي ستايرين والانظمة الاسفلتية المحضرة.4 - اضافة الكبريت بنسبه المختلفة (5%،10%،15%) وزنا الى النماذج المستحصل عليها من المعالجات سابقة الذكر بهدف زيادة قابلية الاذابة للبولي ستايرين في الانظمة الاسفلتية ودراسة المورفولوجي Morphology باستخدام المجهر لملاحظة كيفية توزيع وانتشار البوليمر خلال الاسفلت.5 - تجزئة كل من اسفلت بيجي والقيارة الى مكوناته الاساسية (اسفلتين،راتنجات صلبة،راتنجات لينة) ومعالجة كل مكون من هذه المكونات معالجة كيميائية محفزة مع الكبريت ومن ثم تحويرها بالبولي ستايرين ، ثم يعقبها اضافة الكبريت كل ذلك من اجل ملاحظة اي من هذه المكونات اكثر تمازجا مع البولي ستايرين وتاثرا باضافة الكبريت.وباجراء الدراسات المشار اليها اعلاه وجدنا : * قابلية امتزاج البولي ستايرين بالاسفلت تكون محدودة.* ان خفض الوزن الجزيئي للبولي ستايرين اسهم في زيادة تذاوبه مع الاسفلت الذي ادى بدوره الى الحصول على نماذج اكثر تجانسا.* الانظمة الاسفلتية المحضرة بالمعالجة الكيميائية المحفزة مع الكبريت لكل من اسفلت بيجي والقيارة كانت افضل تمازجا مع البولي ستايرين من الاسفلت غير المعالج كيميائيا.* اضافة الكبريت بنسبه المختلفة (5%،10%،15%) وزنا الى الانظمة الاسفلتية المحورة بالبولي ستايرين وبغض النظر عن طبيعتها ادت الى تحسن تجانسيتها بشكل ملحوظ من خلال زيادة انتشار واذابة البولي ستايرين خلال الانظمة الاسفلتية.* عملية تجزئة كل من اسفلت بيجي والقيارة الى مكوناته الاساسية وتحوير كل من هذه المكونات بالبولي ستايرين ثم بالكبريت اثبتت ان المكون الاكثر ارومية هو الاكثر تمازجا مع البولي ستايرين والاكثر تاثرا باضافة الكبريت ، وهذا ساعدنا في اعطاء تفسير للنتائج التي حصلنا عليها. | Polymer modified asphalts (PMA) became of great interest over the last years, because they are closely related to industrial and constructional fields, as the addition of small amounts of polymer dramatically changes the rheological properties of asphalts. Due to the shortage of studies on polystyrene modified asphalts,the present study is a trial to clarify the behaviour of polystyrene with asphalt.Polystyrene was choosen to modify asphalts due to its properties as a cheap and commonly used thermoplastic polymer,as well as the environ mental problems caused by the huge quantities of its residue.The study includes : - 1 - Treating Beji parafenic asphalt & Qiayarah aromatic asphalt with various percentages of polystyrene as well as chemical reaction between polystyrene and Beji asphalt.2 - Physical & chemical treatment of Beji asphalt with various percentages of thermally cracked polystyrene to establish the effect of molecular weight on the compatibility of polystyrene with asphalts.3 - A preliminary modification of asphalt by a catalyzed chemical reaction with sulphur then the compatibility of these systems with polystyrene were studied.4 - Adding sulphur of different weight percentages (5% , 10% , 15%) to the samples produced by the above mentioned treatments in order to increase the capability of polystyrene to solvate in the asphaltic systems and to study the morphology microscopically to notice the dispersion of polystyrene in asphalt.5 - Fractionating Beji & Qiayarah asphalts into their basic components (asphaltene,hard resins,soft resins) and treating each of these components with sulphur by stimulating chemical treatment. Then ,modified with polystyrene in order to notice which one of these components is the most compatible with polystyrene and the most affected by the addition of sulphur.After conducting the above mentioned studies, it was found that : - * The compatibility of polystyrene in asphalt is limited.* compatibility was increased by decreasing molecular weight of polystyrene.* Better compatibility of polystyrene was obtained with STA.* Adding sulphur with weight percentages (5% , 10% , 15%) to the polystyrene modified asphalt led to increase its homogeneity significantly.* Fractionating of Beji & Qiayarah asphalts into its basic components and modifying these components by polystyrene and then by sulphur proved that the most aromatic component is the most compatible with polystyrene and the most affected component by sulphur in a way that helped in justifying the results of the study.

تحضير بعض المشتقات الحلقية غير المتجانسة الجديدة وبعض متراكباتها مع PVC ودراسة سلوكها الضوئي المحفز == Synthesis of some New Heterocyclic Derivatives and some of their composites with PVC and Study their PhotoCatalytic Behaviour

Author name: نور عبد الرزاق عبد اللطيف
Supervisor name: سعدون عبد الله عودة | عباس جاسم عطيه
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: Arabic
University location: Babylon
First pages:
Abstract: تضمنت هذه الدراسة جزئين, الجزء الاول هو تحضيرمركبات عضوية والجزء الثاني هو تحضير مواد متراكبه عضوية - فيزياويةفي مجال التحضير العضوي تم تحضير مركبات حلقية غير متجانسة جديدة باستخدام بارا امينو حامض البنزويك و2 - نفثول كمواد اولية للحصول على الجزيئات الوسطية والجزيئات النهائية المطلوبة، وفقا لمسارات التفاعلات السبعه المذكورة في ادناه. تم تشخيص المركبات المحضرة باستخدام تقنيات الرنين المغناطيسي الهيدروجيني والكاربون 13 وتحليل العناصر والاشعة السينية والاشعة فوق البنفسجية والفلورة والاشعة تحت الحمراء.المسار الاول : تم تحضير مركب الازو [N1] من تفاعل 2 - نفثول وباراامينو حامض البنزويك عند (0 - 5) سيليزي، تفاعل [N1] مع الايثانول المطلق في وجود حامض الكبريتيك المركز ينتج المركب [N2] الذي منه تم تحضير مشتق ثايوسيميكاربازيد [N3].تم غلق المركب 1،3،4 - ترايازول ثايول من مركب [N3] بعد ذلك تم مفاعلته مع هاليدات الكيل مختلفة ]يوديد المثيل, كلوريد الاليل, كلوريد البنزايل[ لانتاج المركبات [N5 - N7].المسار الثاني : استخدم المركب [N4] في هذا المسار كمادة اوليه حيث تمت مفاعلته مع ادوية امينية مختلفة [سيبروفلوكساسين، باراسيتيمول، بسيوفدرين، الثيوفيلين، كلوروديزيبوكسيد وسولفاديازين] لينتج المركبات [N14 - N8].المسار الثالث : في هذا المسارتم مفاعلة المركب [N1] مع ثيوسيميكاربازيد في وجود فوسفوروس اوكسي كلوريد لاعطاء المركب [N15] والذي تمت مفاعلته مع مشتقات الانلين المختلفة لانتاج المركبات [N20 - N15].المسار الرابع : مركبات الالديهايد الاروماتية [N، N - داي ميثيل امين، م - هيدروكسي بنزيلديهايد، 9 - انثرالدهايد، باراكلورو بنزيلديهايد، بنزيلدهايد وتيريفثالدهايد] فوعلت مع 1،3،4 - ثياديازول امين [N15] في الايثانول المطلق لتعطي مركبات شيف [N21 - N26 ].المسار الخامس : تم مفاعلة المركب [N15] مع ثلاثي ايثيل امين وبروميد البروبرجايل في الايثانول المطلق لينتج المركب [N27] الذي تمت مفاعلته مع مختلف الادوية الامينية [سيبروفلوكساسين، باراسيتيمول، بسيوفدرين، الثيوفيلين، كلوروديزيبوكسيد وسولفاديازين] حيث انتجت مركبات [N33 - N28].المسار السادس : في هذا المسار تم مفاعلة المركب الاستر N2] ] مع هيدريت الهيدرازين ليعطى المركب [N34] والذي تم غلقه لاعطاء مركبات حلقية غير متجانسة خماسية وسداسية الحلقة [N35 - N37] عن طريق التفاعل مع الاسيتايل اسيتون, انهيدريد الماليك وانهيدريد الفثاليك، على التوالي.المسار السابع : في هذا المسار تم تحضير بوليمرات محورة متماثلة [N38, 39] من خلال تفاعل (1،2،4 - ترايازول [N4]، 1،3،4 - ثياديازول [N15]) مع بولي كلوريد الفينيل في وجود البيريدين ورباعي هايدروفوران.وايضا تم تحضير البوليمر المحور غير المتماثل [N40] نتج من تفاعل جزيئتين من هذه المركبات (1،2،4 - تريازول [N4]، 1،2،4 - ثياديازول [[N15) مع بولي كلوريد الفينيل بوجود البيريدين ورباعي هايدروفيوران.اما في مجال تحضير المواد المتراكبه الفيزياوية والعضوية يتضمن مايلي : عمل تحوير لسطح اوكسيد الزنك بتطعيمه بالبوليمر المحور [N39] ثم دراسة فعاليتة الامتزازيه وفعالية التحفيز الضوئي له من خلال امتزاز وتكسير الصبغة بسمارك براون جي BBG من المحلول المائي لها على سطح اوكسيد الزنك المجرد وسطح الماده المتراكبه بدرجات حرارية 293و 298و 303 و308 كلفن . حيث كانت الدرجة الحرارية 293 كلفن هي الافضل في كلا الفعاليتين. تم دراسة التكسير الضوئي للمركب [N38] لمدة ستة ساعات بدرجات حرارية (308,303,298) سيليزي. حيث تم دراسة وقياس اللزوجة والوزن الجزيئي والثباتية لهذه المركبات. ووجد ان عملية التكسير الضوئي تزداد مع زيادة زمن التشعيع مع ارتفاع درجة حرارة التفاعل.ايضا تمت دراسة البلمرة الضوئية للمركب [N4] بوجود اوكسيد الزنك وبدرجات حرارية 298,293 ,303كلفن حيث تم الحصول على البولمر المترابط على السطح في هذه العمليه اما البولمر المستخلص فلم يتم الحصول عليه بهذه الطريقه ربما بسبب قوة الترابط بين سطح الاوكسيد والسلاسل البولمريه المتكونه في هذه العمليه علما ان النوع الاول من البولمر هو المهم لانه يعتبر طريقه لتحضير المواد المتراكبه ذات التطبيقات المهمه | This study involves two parts; first part are organic compounds synthesis and the second part are preparation of composites (physical organic) materials. The organic synthesis part, involves synthesis of new heterocyclic compounds using P - amino benzoic acid and 2 - naphthol as starting materials to produce the intermediates molecules and target molecules. This would involve seven routes as they are presented below. The synthesized organic and inorganic materials were characterized using different technique : 1H - NMR, 13C - NMR, CHNS, X - rays diffraction , UV - Visible spectroscopy, UV - Visible fluorescence spectroscopy, and FTIR spectroscopy. First Route : The azo compound [N1] was synthesized from reaction of 2 - Naphthol and p - amino benzoic acid at (0 - 5) ºC, [N1] reacted with absolute ethanol in presence of concentrated sulfuric acid to give [N2] that afforded compound thiosemicarbazide derivative [N3] . Cyclized triazole thiol was prepared from compound [N3] then reacted with different alkyl halides [methyl iodide, allyl chloride, and benzyl chloride] to give compounds [N5 - N7].Second Route : 1 - ((4 - (5 - mercapto - 4H - 1,2,4 - triazol - 3 - yl)phenyl)diazenyl)naphthalen - 2 - ol [N4] was react with dibromo ethane to synthesis compound [N8]. Also compound [N4] was reacted with different amino drugs [ciprofloxacine, paracetemole, pseuphedrine, theophylline, chlorodizepoxide and sulphadiazine] afforded compounds [N9 - N14].Third Route : Compound [N1] was reacted with thiosemicarbazide in presence phosphorous oxychloride to give 1 - ((4 - (5 - amino - 1,3,4 - thiadiazol - 2 - yl)phenyl)diazenyl)naphthalen - 2 - ol [N15] which reacted with different aromatic amines to yield compounds [N16 - N20].Fourth Route : Aromatic aldehyde compounds [N,N - dimethyl amine aldehyde, m - hydroxy benzyldehyde, 9 - Anthraldehyde, p - chlorobenzyldehyde, benzyldehyde and terephthaldehyde] reacted with 1,3,4 - thiadiazole amine [N15] in absolute ethanol afforded Schiff - base compounds [N21 - N26].Fifth Route : Compound [N15] reacted with triethylamine and proprgyl bromide in absolute ethanol to yield 1 - ((4 - (5 - (prop - 2 - yn - 1 - ylthio) - 1,3,4 - oxadiazol - 2 - yl)phenyl) diazenyl) naphthalen - 2 - ol [N27] which reacted with different amino drugs [ciprofloxacine, paracetemole, pseuphedrine, theophylline, chlorodizepoxide and sulphadiazine] afforded compounds [N28 - N33].Sixth Route : 4 - ((2 - Hydroxynaphthalen - 1 - yl)diazenyl)benzohydrazide [N34] was cyclized to give five and six membered ring heterocyclic compounds [N35 - N37] by reaction with acetyl acetone, maleic anhydride and phthalic anhydride, respectively. Seventh Route : In this route modified homo polymers [N38, N39] were synthesized by reaction of (1,2,4 - triazole [N4], 1,2,4 - thiadiazole [N15],) with polyvinylchloride in the presence of pyridine and tetrahydrofuran (THF). And Modified co - polymers [N40] yield from reaction two molecules from these compounds (1,2,4 - triazole [N4], 1,2,4 - thiadiazole [N15]) with polyvinylchloride in the presences of pyridine and tetrahydrofuran. Physical Organic (composites) route involves : This route involves modifying zinc oxide surface by grafting with 1 - ((4 - (5 - mercapto - 4H - 1,2,4 - triazol - 3 - yl)phenyl)diazenyl)naphthalen - 2 - ol - PVC [N39]. The activity of the produced composites was investigated by adsorption of Bismarck Brown G (BBG) at 293, 298, 303 and , 308 K. The photocatalytic activity of the prepared composite was investigated by following removal of BBG dye via photocatalytic degradation of over the surface at 293, 298, 303, and 308 K. From obtained results, it was found that, the best result for both adsorption and photocatalytic dye removal over the surface was noted at 293 K. Studying the photodegradation of 1 - ((4 - (5 - amino - 1,3,4 - thiadiazol - 2 - yl)phenyl) diazenyl)naphthalen - 2 - ol - PVC polymer [N38] for six hours under irradiation with UV light at 298, 303, and 308 K . Change in molecular weight of these materials were investigated from viscosity measurements and from these measurements their relative stability was investigated. Also, this part involves investigating the photocatalytic polymerization of 1 - ((4 - (5 - mercapto - 4H - 1,2,4 - triazol - 3 - yl)phenyl) diazenyl)naphthalen - 2 - ol) [N4] over zinc oxide at 293, 298,and 308 K. This process yields both grafted and extracted polymer and the first type produces composites materials

الدور الوقائي والعلاجي لفيتاميني C وE على الاجهاد التاكسدي المستحث بواسطة الصبغتين الغذائيتين E102و E122 في ذكور الجرذان == Prophylactic and Protective roles of Vitamin C and E on Oxidative Stress Induced by Food Additives E102 and E122 in Male Rats

Author name: علي نوري فجر المحنة
Supervisor name: لمياء عبد المجيد المشهدي
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: Arabic
University location: Babylon
First pages:
Abstract: صممت هذا الدراسة لمعرفة تاثير صبغتي الكارمويسين (E122) والتترازين (E102) على بعض المعايير الفسلجية لذكور الجرذان والمتضمنة قياس مستوى فعالية الانزيمات المضادة للاكسدة (SOD وGST وGPx) والحالة التاكسدية (MDA وNO وT - AOC) وانزيمات الكبد (AST وALT وALP) وتراكيز اليوريا Urea والكرياتينين Creatinine ومستويات الكوليسترول Cholesterol والدهون الثلاثية Triglycerides والبروتينات الدهنية عالية الكثافة HDL - c وواطئة الكثافة LDL - c فضلا عن قياس التعبير الجيني لانزيم GSTmu, كما تضمنت الدراسة الجانب النسجي لمقاطع الكبد والكلى والمعدة والامعاء للحيوانات المذكورة بهدف التحقق من الدور الايجابي المحتمل لفيتاميني C وE في التقليل من التاثيرات السلبية للصبغات المذكوره اعلاه.نفذت الدراسة في البيت الحيواني التابع لقسم علوم الحياة/ كلية التربية/ جامعة القادسية ضمن المدة (1/ 11/ 2015) وحتى (1/ 3/ 2016)؛ اذ اشتملت على تجربتين الاولى منها ضمت 66 ذكرا من الفئران البيض الناضجة جنسيا وباوزان تراوحت بين (25 - 30) غم واستعملت بغرض تحديد الجرعة المميتة لنصف عدد الحيوانات (LD50). اما التجربة الثانية فضمت 78 ذكرا من الجرذان البيض البالغة جنسيا وباوزان تراوحت بين (225 - 230) غم ومقسمة عشوائيا الى ثمانية مجاميع بحسب كل صبغة (E122 بتركيز 250 ملغم/ كغم من وزن الجسم وE102 بتركيز 500 ملغم/ كغم من وزن الجسم) فضلا عن فيتامين C بتركيز 50 ملغم/ كغم من وزن الجسم وفيتامين E بتركيز 15 ملغم/ كغم من وزن الجسم, وتم تجريعها عن طريق الفم وكالاتي : • مجموعة السيطرة (C) ضمت 6 حيوانات جرعت بماء الشرب الاعتيادي لمدة شهرين.• مجموعة المعاملة الاولى (G1) : ضمت 6 حيوانات جرعت بفيتامين C لمدة شهرين.• مجموعة المعاملة الثانية (G2) : ضمت 6 حيوانات جرعت بفيتامين E لمدة شهرين.• مجموعة المعاملة (G3E122) : ضمت 6 حيوانات جرعت بصبغة E122 وG3E102 ضمت 6 حيوانات جرعت بصبغة E102 لمدة شهرين. • مجموعة المعاملة (G4E122) : ضمت 6 حيوانات جرعت بفيتامين C لمدة شهرين ومن ثم بصبغة E122 وG4E102 ضمت 6 حيوانات جرعت بفيتامين C لمدة شهرين ومن ثم بصبغة E102 لمدة شهرين اخرين. • مجموعة المعاملة (G5E122) : ضمت 6 حيوانات جرعت بفيتامين E لمدة شهرين ومن ثم بصبغة E122 وG5E102)) ضمت 6 حيوانات جرعت بفيتامين E لمدة شهرين ومن ثم بصبغة E102 لمدة شهرين اخرين.• مجموعة المعاملة (G6E122) : ضمت 6 حيوانات جرعت بصبغة E122 ومن ثم بفيتامين E و((G6E102 ضمت 6 حيوانات جرعت بصبغة E102 لمدة شهرين ومن ثم بفيتامين E لمدة شهرين اخرين. • مجموعة المعاملة (G7E122) : ضمت 6 حيوانات جرعت بصبغة E122 ومن ثم بفيتامين C و(G7E102) ضمت 6 حيوانات جرعت بصبغة E102 لمدة شهرين ومن ثم بفيتامين C لمدة شهرين اخرين. بعد نهاية الفترة المحددة لمعاملة الحيوانات بالتراكيز المختلفة للصبغات والفيتامينات تم وزن الحيوانات ومن ثم تخدريها بمادة الكلوروفورم وسحب الدم منها مباشرة من القلب فضلا عن عزل مصل الدم لاجراء الفحوصات المذكورة اعلاه, بعد ذلك شرحت الحيوانات لغرض تحضير المقاطع النسجية منها, واظهرت النتائج حصول ما يلي : 1 - انخفاض معنوي في مستوى فعالية الانزيمات المضادة للاكسدة (SOD وGST وGPx) والبروتينات الدهنية عالية الكثافة في المجاميع (G3 وG4 وG5) مقارنة مع باقي المجاميع الاخرى.2 - ارتفاع معنوي في مستوى فعالية انزيمات الكبد (AST وALT وALP) ومؤشرات وظائف الكلى (اليوريا والكرياتينين) والكوليسترول والدهون الثلاثية والبروتينات الدهنية واطئة الكثافة في المجاميع (G3 وG4 وG5) مقارنة مع باقي المجاميع الاخرى.3 - ارتفاع معنوي في مستوى فعالية الانزيمات المضادة للاكسدة (SOD وGST وGPx) والبروتينات الدهنية عالية الكثافة وانزيمات الكبد (AST وALT وALP) ومؤشرات وظائف الكلى (اليوريا والكرياتينين) والكوليسترول والدهون الثلاثية والبروتينات الدهنية واطئة الكثافة في المجموعتين (G6 وG7) مقارنة بالمجاميع (G3 وG4 وG5), في حين لم تظهر فروق واضحة عند مقارنتها مع مجموعة السيطرة (C).4 - انخفاض معنوي في التعبير الجيني لانزيم GSTmu في المجاميع (G3 وG4 وG5) مقارنة مع المجموعتين (G6 وG7) التي اعطت ارتفاعا معنويا في التعبير الجيني للانزيم والتي بدورها لم تختلف معنويا مع مجموعة السيطرة (C).5 - تغيرات نسجية مرضية شملت موت وتنخر ونزف في المقاطع الماخوذة من الكبد والكلية والمعدة والامعاء في المجاميع (G3 وG4 وG5) مقارنة مع باقي المجاميع الاخرى التي لم تظهر اختلافات نسجية واضحة فيما بينها. | The current study was designed to determine the effect of carmoisine (122) and tartrazine (102) dyes on some physiological criteria for white rats male and included measuring the level of effectiveness of antioxidant enzymes (SOD, GST and GPx), phosphorylation status (MDA, NO and T - AOC), liver enzymes (AST, ALT and ALP), the concentrations of urea, creatinine and the levels of cholesterol, triglycerides, high density lipoprotein (HDL) and low density lipoprotein (LDL); as well as a measure of gene expression for GSTmu enzyme. Also the study included histology to liver, kidneys, stomach and intestines of mentioned animals in order to verify the potentially positive role of vitamins C and E in reducing from the negative effects to above mentioned dyes.The present study was conducted in the animal house of the department of biology/ College of Education/ University of Al - Qadisiyah within the period (1/11/2015) till (30/3/2016); it included on two experiments; the first experiment which included 66 male of sexually mature white mice with weights between (25 - 30) g and is used in order to determine lethal dose of half the number of animals (LD50). The second experiment included 78 male of sexually mature white rats with weights between (225 - 230) g and divided randomly into eight groups according each dye (E122 a concentration of 250 mg/ kg of body weight and E102 a concentration of 500 mg/ kg of body weight) as well about of vitamin C with concentration of 50 mg/ kg of body weight, vitamin E with concentration of 15 mg/ kg of body weight, as follows : • Control group (C) included 6 animals with doses by ordinary drinking water for six weeks.• First treatment group (G1) : 6 animals included with doses by vitamin C for two months.• Second treatment group (G2) : 6 animals included with doses by vitamin E for two months.• treatment group (G3E122) : 6 animals included with doses by E122 and G3E102 6 animals included with doses by E102 dye for two months.• treatment group (G4E122) : 6 animals included with doses by vitamin C for two months and then E122 dye for a two months. and G4E102 animals included with doses by vitamin C for two months and then E102 dye for a two months.• treatment group (G5E122) : 6 animals included with doses by vitamin E for two months and then E122 dye for a two months. and G5E102 animals included with doses by vitamin E for two months and then E102 dye for a two months.• treatment group (G6E122) : 6 animals included with doses by E122 dye for two months and then vitamin E for two months and G6E102 6 animals included with doses by E102 dye for two months and then vitamin E for two months• treatment group (G7) : 6 animals included with doses by E122 dye for two months and then vitamin C for two months and G6E102 6 animals included with doses by E102 dye for two months and then vitamin C for two monthsAfter the end of the period specified for the treatment of animals by different concentrations of the dyes and vitamins taking the weight of animals and then were Anesthetization and blood draw directly from the heart as well as the blood serum were isolation to conduct the all tests listed above, then the animals were anatomy to purpose of the histological sections preparation, and the results showed the following : 1 - A significant decrease in the level of antioxidant enzymes effectiveness (SOD, GST and GPx) and HDL in groups (G3, G4 and G5) compared with the other groups.2 - A significant increase in the level of liver enzymes effectiveness (AST, ALT and ALP) and indicators of kidney function (urea and creatinine), cholesterol, triglycerides and LDL in groups (G3, G4 and G5) compared with the other groups.3 - A significant increase in the level of antioxidant enzymes effectiveness (SOD, GST and GPx), HDL, liver enzymes (AST, ALT and ALP), indicators of kidney function (urea and creatinine), cholesterol, triglycerides and LDL in two groups (G6 and G7) compared with groups (G3, G4 and G5), while did not appear significant differences when compared with the control group (C).4 - A significant decrease of gene expression to GSTmu enzyme in groups (G3, G4 and G5), compared with two groups (G6 and G7), which gave increased significantly in the gene expression of the enzyme, which in turn were not significantly different with the control group (C).5 - Histo - pathological changes were included degeneration, necrosis and hemorrhage in the sections were taken from the liver, kidney, stomach and intestines in groups (G3 and G4 and G5) compared with the other groups that are did not appear histological differences among them.

فصل انزيم اللايبوكسيجينيز من مصل الرجال الاصحاء ومعاملة خارجية للانزيم في مرضى الربو == Separation of Lipoxygenase from Sera of Healthy men and in Vitro Treatment of Enzyme in Asthmatic Patients

Author name: احمد جياد عباس البرقعاوي
Supervisor name: عودة مزعل ياسر الزاملي
General topic: Chemistry
Specific topic: Analytical Biochemistry
Degree: Doctorate
Language: English
University location: Babylon
First pages:
Abstract: This study is concerned with asthma. Sixty seven asthmatic male patients were examined and tested , their age ranged from 10 - 65 years and they previously diagnosed as asthmatic patient under the physician supervision in AL - Hilla center of Allergy and Asthma . They have the disease for more than five years. Forty patients were examined during the period between July2015 to October 2015, and twenty seven patients were examined during period between June to August 2016, also the control group consisted of sixty seven healthy males ranged from 10 - 65 years.In this study asthmatic patients were divided into three groups according to medication , the first group consisted of (17) asthmatic patients taking antihistamines such as loratadine , citrizine and allermine , while the second group included (24) asthmatic patients taking montelukast , and the third group included (26) asthmatic patients who were on different drugs other than antihistamines and montelukast such as steroids and beta agonists .Five milliliters of blood were obtained from each patient, serum collected absolutely free from hemolysis stored at - 20 °C until uses for measurement of the concentrations of Glutathione, Malondialdehyde, Catalase, Histamine, Serotonin, Lipoxygenase - 5, Leukotriene A4 Hydrolase, total Immunoglobulin E and specific immunoglobulin E.The results revealed that the mean of IgE level (measured by ELISA system)in serum of asthmatic group was (368.16 ±1.772 ng/ml) versus the control group (138.9±2.515 ng/ml) with a significant difference,)P < 0.001(. Asthmatic patients and patients treated with pharmacological drugs such as montelukast and antihistamines showed high sensitivity to some food, animals, plant, palm pollen, fungal and mite allergen and they showed different values between patients and control. The study showed that there is no association between the increased sensitization to food, animal, plant and fungal allergens with age of patients.The present study showed the relationship of count blood cells (WBC and RBC) in studied groups. In all studied groups, WBC values higher than control group while the RBC values showed little differences among all studied groups.According to levels of some variables (histamine, serotonin, LOX - 5 and LTA4H) in asthmatic patients, the results showed a higher mean value of serotonin in asthmatic patients (0.023± 0.004 ng /ml) compared with control group (0.002± 0.001 ng/ml, p˂0.001) In addition the value of histamine was observed high in asthmatic patients (8.511± 0.410 ng /ml)while the control group was (2.565 ± 0.140 ng/ ml) with a significant difference of the mean value of histamine between asthmatic patients and control group (p˂0.001). LOX - 5 level in serum of asthmatic patients was higher (11.080 ± 0. 190 ng/ml) than in control group (9.821 ± 0.203 ng/ml, p˂0.001.The data revealed significant high mean value of LTA4H in asthmatic patients (24.148 ± 0 .450 ng/ml) compared with control group (18.912 ± 0.459 ng/ml, p˂0.001).The result showed that histamine level was increased in the group (>40 years) with a mean value (9.67 ± 4.25 ng /ml ) . While LOX - 5 showed high mean value (11.532 ± 1.274) in the group 20 - 40 years . Also LTA4H enzyme showed high mean value (25.54 ± 3.504 ng/ml)in the group 20 - 40 years , while serotonin appeared with high mean value (0.027± 0.015 ng/ml) in the group (< 20 years) with a significant difference between levels of these variables in each age group (p ˂ 0.001)The mean concentration of an antioxidant, Glutathione(GSH), and Malondialdehyde (MDA) in serum of asthmatic patient and control groups. The mean concentration of MDA increased in asthmatic patients (11.317 ± 1.096 μmol/l) more than control group(8.733 ± 3.756 μmol/l)with a significant difference between these groups (p < 0.05). The mean concentration of GSH increased was in the control (5.106 ± 3.197 μmol/l) more than asthmatic patients(3.905 ± 1.638 μmol/l, p < 0.05).According to the results of the present study, the mean activity of catalase(CAT) was higher (1.555±0.982 U/l) in asthmatic patients when compared with control group(1.173 ± 0.502 U/l, p < 0.05).The current study also concerned with the extrection of lipoxygenase from serum of asthmatic patient and healthy men by taking 15 ml serum from ten asthmatic patients men and 15 ml from serum of ten healthy men. And these quantities of serum were precipitated by ammonium sulfate, The best ratio for precipitating serum and extraction of enzyme is 60%. The anion exchange chromatography was used for extraction of the enzyme. The molecular weight of the extracted enzyme was determined by SDS - PAGE . In this procedure one subunit of the extracted LOXs enzyme showed a molecular weight of 35KD for one chain while a recombinant pure human LOX - 5 showed a molecular weight of 38 KD. The current study used NATIVEN technique for purification of the extracted enzyme obtained from ion exchange chromatography.The results revealed the optimum pH and temperature for LOXs activity and they were 8 and 40°C, respectively.The velocity constant and maximum velocity of the extracted Lipoxygenase enzyme was detected by using PHYWE SYSTEME GMBH SYSTEM, this system had the ability to obtain the relationship between conductivity and concentration (an increase in concentration lead to an increase in conductivity).The extracted lipoxygenase enzyme Km was 2.2mM and Vmax= 140mM/min in asthmatic patients and Km was 2.7mM and Vmax= 135mM/min in controls (by applying Michaelis - Menten equation).While the enzyme Km= 5.5mM and Vmax= 238mM/min in asthmatic patients and Km= 5 mM and Vmax= 208 mM/min in controls (by applying Lineweaver - Burk equation).The extracted LOXs from asthmatic patients and controls was treated with montelukast. The Km and Vmax appeared to have low values Km 3.6mM and Vmax 153mM/min and Km 3.7mM and Vmax 147mM/min, respectively. Also the extracted LOXs from asthmatic patients and controls was treated with molsiodomine, showed low values Km 4.4mM and Vmax 182 mM/min and Km 4.3mM and Vmax 166 mM/min, respectively.

تحضير ودراسة طيفية ومعالجة نظرية لمعقدات مزيج ليكاندي مشتقات البنزاميدازول والفينانثرولين

Author name: دعاء حبيب محل
Supervisor name: محاسن فيصل الياس
General topic: Chemistry
Specific topic: Organic Chemistry
Degree: Doctorate
University: University of Baghdad
Language: Arabic
University location: Baghdad
Key words:
  • تحضیر
  • حلقیة غیر متجانسة
  • جالكون، بایرازولین
  • ثنائي هایدروبایرمدین - - 2 اون
  • ثنائي هایدروبایرمدین - 2 - ثایون، بولي ایماید
  • فعالیة بایولوجیة
  • موجات فوق صوتیة Synthesis
  • Heterocyclic
  • Chalcone
  • derivatives
  • Pyrazoline
  • Dihydropyrimidin - 2 - one
First pages:
Abstract: In this study, two new aromatic chalcones have been synthesized. The first one contain one amino phenyl group while the second contain two amino phenyl groups , from the reaction of 2 - acetothiophene or pamino acetophenone with p - or m - amino benzaldehyde respectively by Claisen - Schmidt condensation in alcoholic base medium (10%NaOH ).Also, some of heterocyclic compounds have been derived from these prepared chalcones as a derivatives for 2 - pyrazoline ring and for dihydro pyrimidine - 2 - one/thione as follows : 1 - Preparation of 3,5 - di (amino phenyl ) - 2 - pyrazoline (3,9) derivatives from condensation of (1,2) chalcone with hydrazine hydrate in absolute ethanol.2 - Preparation of 3,5 - di (amino phenyl) - 1 - phenyl - 2 - pyrazoline (4,10) derivatives by the reaction of chalcone (1,2)with phenyl hydrazine in presence of acetic acid.3 - Preparation of 3,5 - di (amino phenyl) - 1 - substituted - 2 - pyrazoline (5 - 7,11 - 13) from the reaction of chalcones (1,2) with semicarbazide, thiosemicarbazide and isoniazide in strong basic medium (45% NaOH) in absolute ethanol.4 - Preparation of 4,6 - di(amino phenyl ) - 3,4 - dihydro pyrimidine - 2 - one / thion (14,15) : from the reaction of chalcone(2)with urea and thiourea in presence of sodium ethoxide in absolute ethanol in two ways : thermal catalyse and ultrasonic waves with high yield for the last one.The phenyl amines derivatives (3 - 7,9 - 15)included benzidine (8) were converted into N - substituted maleimic acid (16 - 28) , by reacted it with maleic acid anhydride in ether or dry acetone.These derivatives (16 - 28) were undergo dehydration by using anhydrous acetic and sodium acetate to give N - substituted malimide products ( 29 - 41) in good yield.Also, the homopolymers (42 - 54) for these malimides were prepared by free radical polymerization with benzoyl peroxide as initiator and dimethyl formamide (DMF) as a solvent at 130 0C. PDF created with pdfFactory Pro trial version www.pdffactory.com The copolymers (55 - 104)have been prepared by the samemethod and initiator with vinyl acetate for polymers (55 - 67)and with acryl amide for polymers (68 - 72) and with allyl benzene for polymers (73 - 80) and with maleimide (31) for the polymers (81 - 88) , also with maleimide (32) for the polymers (89 - 96) and finally with maleimide (33) for the polymers (97 - 104).The structures of these new compounds were characterized by UV spectra (as a comparable study for unpolymered molecules ),IR (infra - red ) spectra and 1H - NMR (nuclear magnetic resonance ) spectra for some of the prepared compounds and followed by TLC (thin layer chromatography ).The stability of these compounds (9 - 12) were studied spectrally from the changing in its high absorbance values (peaks) ?max for their solutions at concentrations 2×10 - 5M in light and dark with time for comparability. These compounds showed good stability whichcan be suggested to be used as an organic reagents for analytical study especially with drugs and phenolic compounds.More ever, the identification study , here we have studied the heoretical study of formation heat for intermediates and final compounds bodies length of the bond which was agreement with the particularly results.This study ,also includes the biological activity for some of the prepared compounds against four kinds of germs which known by its resistance against antibiotics ,these are Staphylococcus aureus (positive for Gram stain )and Escherichia coli ,Pseudomonas aeruginosa and Salmonalla typhi (negative for Gram stain ) and studiesy the inhibition values for these compounds comparable with three of standard antibiotics as controls (ampicilline : C1, Cloxacilin : C2, erythromycin : C3) , and the results show the ability of these prepared compounds to inhibit all the used germs except Pseudomonas which shows clear resistant for less polarity comparable with control samples.

دراسة مستوى انزيم الرينيين والفا - ل - فيوكوز وبعض المتغيرات الكيموحيوية للمرضى المصابين بالعجز الكلوي المزمن == Level of Renin Enzyme, ? - L - Fucose And Some Biochemical Markers For Chronic Renal Failure Patients

Author name: سروت بهرام عارف محمود الكاكةئي
Supervisor name: صباح حسين خورشيد
General topic: Chemistry
Specific topic: Biochemistry
Degree: Doctorate
Language: Arabic
University location: Salahaddin
First pages:
Abstract: خلفيه البحث : سوفان المفاصل هو مرض مزمن يؤدي الى حدوث تغيرات ضارة في الغضاريف والعظام والاربطة والعضلات , علما ان وصف المرض بشكل دقيق غير محدد لحد الان. والسؤال المطروح عن العلاقة بين العلامات الناتجة عن هذا المرض وتلك الناتجة عن مرض السكري, هل الام السك | خلفيه البحث : سوفان المفاصل هو مرض مزمن يؤدي الى حدوث تغيرات ضارة في الغضاريف والعظام والاربطة والعضلات , علما ان وصف المرض بشكل دقيق غير محدد لحد الان. والسؤال المطروح عن العلاقة بين العلامات الناتجة عن هذا المرض وتلك الناتجة عن مرض السكري, هل الام السكري تخفي الام المفاصل ؟ حيث ان كلا المرضين(السكري والمفاصل) هما من الامراض المزمنة وتتصف بمستويات غير واضحة من التغيرات البايولوجية للمريض.الهدف من البحث : صممت هذه الدراسة لايجاد العلاقة بين داء السكري وسوفان المفاصل من خلال دراسة بعض المتغيرات الحياتية المشتركة بين المرضين مثل الفسفاتين واللبتين وهرمون النمو المشابه للانسولين... , وايضا دراسة تاثير داء السكري على تطور سوفان المفاصل. العينات, المواد وطرائق العمل : تضمنت هذه الدراسة (88)عينة مرضية من النساء فقط تراوحت اعمارهم (40 - 60) سنه ,في بداية التشخيص لمرض سوفان المفاصل من المصابين وغير المصابين بداء السكري الذين يعانون من السمنه)وقد تم جمع العينات من مستشفى الكاظمية التعليمي والمركز الوطني لبحوث وعلاج السكري / مستشفى اليرموك,من شهر ايار - تشرين الاول(2013 ) وقد تم تقسيم عينات المرضى الى ثلاث مجاميع وهي( مجموعة سوفان المفاصل وعددهم 24)و(مجموعة داء السكري وعددهم 20عينه)و(المجموعة الحاملة كلا المرضين عددهم 24عينه) فضلا عن مجموعة السيطرة وعددهم (20عينه) وقد تم تقدير مستويات الدوال في امصال العينات من خلال اجراء الفحوصات المختبرية التالية : هرمون الفس?اتين, هرمون االلبتين, هرمون النمو الشبيه بالانسولين - 1,مستوى الانسولين الصائم , هرمون المناسل المحفز الجربي FSH والمحفز للجسم الاصفر LH , مؤشر معصد البلازما بوساطه العلاقة اللوغاريتمية المتمثلة بالكسر المولي للدهون الثلاثية والدهون عالية الكثافة وفحص مقاومه الانسولين,وفحص السكر الصائم, الدهون في الدم وخضاب الدم المعسل والتي تم قياسها لجميع المرضى وافراد مجموعة السيطرة.النتائج : كانت النتائج المستحصلة من هذه الدراسة كما يلي : ? اظهر المستوى االمصلي للفسفاتين واللبتين وكذلك قيم مؤشر معصد البلازما زياده معنويه في مجاميع المرضى الثلاث وهي (داء السكري , سوفان المفاصل والذين يعانون كلا المرضين) بمجموعه السيطرة بمستوى احتماليه p< 0.05)),في حين لوحظ انخفاض معنوي لدى المرضى الذين يعانون من كلا المرضين (السكري والسوفان) في حالة اخذ الدواء مقارنة بالمرضى بدون دواء تحت احتماليه p< 0.05)).? اظهر المستوى المصلي لهرمون النمو الشبيه بالانسولين انخفاض معنوي في مجاميع المرضى الثلاث وهي (داء السكري , سوفان المفاصل والذين يعانون كلا المرضين) بمجموعه السيطرة تحت احتماليه p< 0.05)), في حين لوحظت زيادة معنوية لدى المرضى الذين يعانون من كلا المرضين (السكري والسوفان) في حالة اخذ الدواء مقارنة بالمرضى بدون دواء تحت احتماليه p< 0.05)), ووجد ايضا ان عامل العمر له تاثير " كبير جدا على قيم مؤشر معصد البلازما ومستوى الفسفاتين ,اللبتين وهرمون النمو الشبيه بالانسولين.? اظهر انخفاض معنوي في مستوى نسبة LH/ FSH في مجاميع المرضى الثلاث وهي (داء السكري , سوفان المفاصل والذين يعانون كلا المرضين) بمجموعه السيطرة تحت احتماليه p< 0.05)), في حين وجدت زياده معنوية في مستوى نسبة LH/FSH في مجموعة المرضى اللذين يعانون من كلا المرضين مقارنة بمجموعة مرضى السكري ومجموعة سوفان المفاصل ولوحدها. ? مستوى الفسفاتين يرتبط ايجابيا مع قيم مؤشر معصد البلازما في مجموعة مرضى داء السكري والمجموعة اللذين يعانون كلا المرضين تحت احتماليه p< 0.01)),في حين لايوجد ارتباط بين مستوى الفسفاتين وقيم مؤشر معصد البلازما في مجموعة مرضى سوفان المفاصل ومجموعة السيطرة. ? اظهر مستوى هرمون النمو الشبيه بالانسولين ارتباطا سلبيا مع قيم مؤشر معصد البلازما عند مجاميع المرضى الثلاثة ( داء السكري , سوفان المفاصل وكلا المرضين) تحت احتماليه p< 0.01)), لكن لايوجد ارتباط مع مجموعة السيطرة. ? اظهر مستوى اللبتين ارتباطا ايجابيا مع قيم مؤشر معصد البلازما عند مجاميع المرضى الثلاث ( داء السكري , سوفان المفاصل وكلا المرضين) تحت احتماليه p< 0.01)), لكن لايوجد ارتباط مع مجموعة السيطرة.? وايضا وجد ارتباط سلبي بين مستوى الفسفاتين ومستوى اللبتين عند المجموعة الحاملة كلا المرضين داء السكري وسوفان المفاصل تحت احتماليه p< 0.01)),في حين كان هناك ارتباطا ايجابيا بين مستوى الفسفاتين ومستوى اللبتين عند مجموعة السكري ومجموعة سوفان المفاصل ولوحدها تحت احتماليه p< 0.01)), وقد وجد ايضا ارتباطا سلبيا بين مستوى الفسفاتين ومستوى هرمون النموالشبيه بالانسولين عند مجاميع المرضى الثلاث تحت احتماليه p< 0.01)) , ولايوجد ارتباط مع مجموعة السيطرة. ? اظهر ارتباطا ايجابيا بين مستوى نسبة LH/FSH وكل من مستوى الفسفاتين , اللبتين وهرمون النمو الشبيه بالانسولين عند مجاميع المرضى الثلاث تحت احتماليه p< 0.01)), لكن لايوجد ارتباط في مجموعة السيطرة. الاستنتاج : نستنتج ان سوفان المفاصل له تاثير مباشر على بعض المؤشرات الحياتية مثل مستويات هرموني اللبتين والفسفاتين واختلال الدهون وقيم مؤشر معصد البلازما. ومن اهم النتائج ان الفسفاتين مؤشر جيد لدراسة تطور المرض ومن الممكن استخدامه كوسيلة للعلاج وكذلك نستنتج ان السيطرة على مستويات السكر عند مرضى سوفان المفاصل مهم جدا خلال العلاج وبالاخص لو تطلب الامر اجراء عملية جراحية.

تحضير وتشخيص بعض مشتقات السكارين العضوية ومعقدات السكارين ومشتقاته الفوسفينية مع بعض الفلزات == Synthesis And Characterization Some of Organic Saccharin Derivatives And Metal Complexes of Saccharin And Its Phosphine Derrivative

Author name: عفراء صابر شهاب الزوبعي
Supervisor name: احمد عبد الحسن احمد الكاظمي | صبحي عطية محمود الجبوري
General topic: Chemistry
Specific topic: Organic Chemistry
Degree: Doctorate
Language: Arabic
University location: Salahaddin
First pages:
Abstract: تضمن البحث تحضير عدد من الادوية المصاحبة المشتقة من مضادات التهاب غير ستيرويدية تم الحصول عليها من معمل ادوية سامراء هي الايبوبروفين، الاندوميثاسين، النابروكسين، الاسبرين، الكابتوبريل والايزونوزايد. عملية تحوير ال | In this study, a number of prodrugs have been synthesized starting from Non - steroidal anti inflammatory drugs such as Ibuprofen, Indomethacin, Naproxen, Aspirin, Captopril and Isoniazid. The modification process started from the conversion of carboxyl group which is existing in these drugs (except in Isoniazid) into esters, chlorides and acid hydrazide.The drugs have been linked to each other and to itself via amide linkage through the reaction of their acid chlorides and acid hydrazides to afford 1,2 - diacyl hydrazine derivatives(M17 - M27). Some acid hydrazides have been treated with isophthaloyl chloride to Benzene - 1,3 - dicarbo hydrazide - 1,3 - Bis substituent(M28 - M30). The same hydrazides have been treated with Benzen - 1,3,5 - tri carbonyl tri chloride to afford Benzen - 1,3,5 - tricarbhydrazide - 1,3 - Tris substituent (M31 - M33). Compounds M28 and M29 have been treated with POCl3 to afford Bis - substituent - 5 - phenyl - 1,3,4 - Oxadizole(M34 - M35). Another modification onto drugs has been done through the linking of these drugs with quinazoline nucleus through amide linkage to afford N - (4 - oxo - 2 - phenylquinazolin - 3(4H) - yl)amide - substit derivatives (M38 - M42). Another modification has been carried out through the reaction of hydrazides with Aromatic aldehydes to afford the mono hydrazide - hydrazones derivatives or Schiff's bases (M43 - M65) and di hydrazide - hydrazones derivatives in which two moles from hydrazide have been treated with one mole of dialdehyde(M66 - M73). In addition, new hydrazones have been synthesized through the reaction of hydrazides with Isatin nucleus which is well known as biological active center to afford the compounds (M74 - M77) with good biological activity. Benzodiazepines have been obtained through the reaction of Isoniazid hydrazones with glycene phthalimide and p - aminobenzoic acid(M82 - M92). Indomethacin hydrazones have been treated with acetic anhydride to afford 1 - [2 - (substituent) - 5 - (5 - methoxy - 2 - methyl - 1H - indol - 3 - ylmethyl) - [1,3,4]oxadiazol - 3 - yl] - ethanone derivatives (93 - M97). The Derivatives of 5 - substit - 2 - Mercapto - 1,3,4 - Oxadiazole(M98 - M103) have been obtained through the reaction of the drug hydrazides with CS2 in the presence of KOH. The oxadizoles have been treated with hydrazine hydrate to afford 4 - amino - 5 - sub - 4H - 1,2,4 - triazole - 3 - thiol derivatives for the Non - steroidal anti - inflammatory drugs(M104 - M107). In addition, 5 - sub - 1,3,4 - Oxadiazole - 2 - amine derivatives have been obtained through the reaction of drug hydrazides with BrCN(M108 - M111). The compound 5 - {1 - [4 - (2 - methylpropyl)phenyl]ethyl} - N3 - phenyl - 4H - 1,2,4 - triazole - 3,4 - diamine (M113) has been synthesized through the reaction of the compound 2 - {2 - [4 - (2 - methylpropyl)phenyl]propanoyl} - N - phenylhydrazinecarbothioamide (M112) with hydrazine hydrate. The ester compound 2 - hydroxyphenyl 2 - [4 - (2 - methylpropyl)phenyl]propanoate (M114) have been obtained through the reaction of Ibuprofen chloride with salicylic acid. The two compounds, 2 - (4 - Isobutyl - phenyl) - propionic acid [1 - (4 - methyl - piperazin - 1 - ylmethyl) - 2 - oxo - 1,2 - dihydro - indol - 3 - ylidene] - hydrazide (M115) and 2 - (4 - Isobutyl - phenyl) - propionic acid [5 - fluoro - 1 - (4 - methyl - piperazin - 1 - ylmethyl) - 2 - oxo - 1,2 - dihydro - indol - 3 - ylidene] - hydrazide (M116) have been obtained through the reaction of M74, M77 with excess of formaldehyde and equimolar of N - methyl piperazine.The synthesized compounds have been identified using Infra - red spectroscopy FTIR, Nuclear Magnetic resonance (1H,13C), Mass spectroscopy and X - Ray. In addition , the changes in physical properties such as melting points, boiling points and color have been considered. Finally, the biological activity of some synthesized compounds has been evaluated and some of them have shown good biological activity especially those containing Isatin nucleus (M74 - M77) and (M115 - M116).

تحضير وتشخيص مشتقات جديدة للاندنول تحمل حلقات غير متجانسة متنوعة == Synthesis And Characterization of New Indole Derivatives Bearing Various Hetero Rings

Author name: كاظم ماذي لازم العلياوي
Supervisor name: جمبد هرمز توما | خالد فهد علي
General topic: Chemistry
Specific topic: Organic Chemistry
Degree: Doctorate
Language: English
University location: Qadisiyah
First pages:
Abstract: تتضمن هذه الاطروحة تحضير وتشخيص بعض مشتقات السكارين العضوية ومعقدات السكارين ومشتقاته الفوسفينية مع بعض الفلزات، حيث استخدم سكارينات الصوديوم والسكارين كمواد اولية للتحضير وكما ياتي : 1 - حضر N - كلور اسيتل سكارين (A2) من تفاعل السكارين مع كلور استيل كلور | This thesis include synthesis and characterization of some organic saccharin derivatives and metal complexes of saccharin and its phosphine derivatives are synthesized in this work according to the following : 1. The N - Chloro acetyl saccharin (A2) is prepared from the reaction of saccharin with chloro acetyl chloride, in presence of Et3N in 1,4 Dioxan. The N - (2 - aryl amino) acetyl saccharine (A3 - A9) is synthesized from the reaction of compound (A2) with the substituted amin.The N - (2 - Saccharin - 2yl) acetyl saccharine A(10) is prepared from reaction of two mole saccharin with mole chloro acetyl chloride in presence of Et3N in 1,4Dioxin.2. Mannich Bases (A11 - A26) are prepared from the reaction of saccharin with substituted primary amin and fromaldehyde in methanol.3. N - Hydroxy methyl saccharin (A27) is prepared from the reaction of saccharin with formaldehyde in H2O or EtOH. The N - methylacetat saccharin (A28) is prepared from the reaction of compound (A27) with acetic anhydride in the presence of NaOH.4. (3 - Benzosulfonamide2 - Carboxylicacid2 - yl)2 - imino thiazolidin - 4 - (one) (A29) is prepared from the reaction of compound (A2) with KSCN in acetone.5. N - Benzoyl Saccharin (A30) is prepared from the reaction of saccharin with Benzoyl Chloride in acetone in the presence of NaHCO3.6. N - acetyl Saccharin(A31) is prepared from the reaction saccharin with acetyl chloride in DMF in the presence of Et3N also N - acetyl saccharin (A49) is prepared from the reaction of sodium saccharin with acetyl chloride in DMF. The N - acetyl saccharine is used in the preparation of ? - ? - Unsaturated carbonyl compounds(A50 - A54) through its reaction with substituted benzaldehyde , and also N - acetyl saccharin is used in the preparation of Schiff bass A(55 - 58) through its reaction with substituted amine.7. N - acetonyl saccharin (A32) is prepared from the reaction of sodium saccharin with chloro aceton in DMF. The N - acetonyl saccharin is used in the preparation of Schiff base A(33 - 38) through its reaction with substituted of amine and also N - Acetonyl saccharin is used in the.preparation.of? - ? - Unsaturated.carbonyl.compound(A39 - A45) through its reaction with substituted benzaldehyde.8. N - saccharinato acetic acid (A46) is prepared from the reaction of sodium saccharin with chloro acetic acid in DMF. The N - saccharinato acetic acid used in the preparation of 5 - (N - Saccharin) methyl )2 - amino - 1,2,3 thiadiazol (A47) through its reaction with thio semicarbazide in toluene and also N - Acetic acid saccharin is used preparation of N - ((1H - benzo[d]imidozol - 2yl)methyl) Saccharin (A48) through its reaction with O - Phenyl diamine.9. N - 3 - bromopropyl saccharin (A59) is prepared from the reaction of sodium saccharin with 1,3 dibromopropan in DMF.10. 2 - ChloroN - (4 - (2 - methaoxazol - 5yl)sulfamoyl)phenyl)acetamide (A60)is prepared from the reaction of4 - aminosulphamethaoxazol with chloroacetyl chlorid in 1,4dioxan in the presence of Et3N.2 - saccharin - N(4 - (2 - methyloxazol - 5yl)sulfamoyl)phenyl acetamide(A61)is.prepared from the reaction of sodium saccharin with (A6o)in DMF11. N - ethyl acetate saccharin A(62) is prepared from the reaction of sodium saccharin with chloro ethyl acetate in DMF. The N - acetic acid saccharin (A63) is prepared from the acidic hydrolysis of N - ethylsaccharin acetate by HCl , CH3COOH.The N - (acetyl thiosemicarbazide)saccharine(A64) is prepared from in the reaction of thiosemicarbazide with (A62)in acetone.The 5 - ((N - Saccharin )methyl) - 1,3,4 - thiadiaezol A(65) is synthesized in ring closur reaction by compound (A64) by sulfuric acid.12. N - Diphenyl phosphin saccharin (66) is prepared from the reaction of sodium saccharin with chloro diphenyl phosphine in dry ether. The N - diphenyl phosphin saccharin is used in the preparation of the complexe of the type [M CL2L2] , M=Pt(II) , Pd(II), Ni(II), L = Diphenyl phosphin saccharin [A70 - 72] through its reaction with Na2PdCl4 , PtCl2(DMSO)2,NiCl2 - 6H2O in CH2Cl2 or aceton in which N - Phenyl phosphin saccharin Ligands berhaves as amono dentat and coordinat through (P) atom to Metal.13. Aqua saccharin complexes of the type [M(Sac)2(H2O)4] 2H2O , (M=Ni,Co,Fe,Zn,Mn,Cd,Cu)(A73 - 79) are prepared from reaction sodium saccharin with divalent metal ions from (Ni,Co,Fe,Zn,Mn,Cd,Cu) in which saccharin Ligands behave amono dentate and coordinate through (N) atom to metal.Treament of (dppe , dppm) with aqua saccharinat complexes(A80 - A88) in CH2Cl2 gave complexes of this type.The treatment of dppe with aqua saccharinat complexes of the (Cd,Zn,Fe,Mn)(A79,A78 ,A76,A75)give complexes (A80 - A83)of this type [M(Sac)2(dppe)2], the dppe in these complexes coordinate as abidentate. but treatment of dppe with aqua saccharinat of the (Ni,Co)(A73,A74) gave complexes (A84,A85)of this type [M(Sac)2(dppe)], but treatment of dppe with aqua saccharinat complexes of the (Cu)(A77) , gave complexes(A86) of this type [Cu(Sac)dppe]. The treatment of dppm with aqua saccharinato complexes of the (Cd,Zn)(A78,A79) gave complexes (A87,A88) of this type [M(Sac)2(dppm)2].The structure of the synthesized compound are confirmed by I.R , H1 - N.M.R,C13 - N.M.R,Elemental analysis , molar conductivity and some chemical physical data.

تحضيروتشخيص بعض المشتقات الجديدة لثنائي هيدروبريميدينون باستخدام تفاعل بكينيلي ودراسة فعاليتها البايلوجية == Synthesis And Characterization And Biological Activity Study of Some New Dihydropyrimidinones Derivatives Via Application Biginelli Reaction

Author name: احمد ماهر فهيم
Supervisor name: نبيل عبد عبد الرضا
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: Arabic
University location: Qadisiyah
First pages:
Abstract: The present work involved synthesis of new indole derivatives containing other heterocyclic ring. These derivatives could be divided into the following parts : 1. The first part involved synthesis and characterization of novel 1,3 - diazidine[XIII]a - d and [XIV]a - d by the following steps : Scheme(1).a. Synthesis of 3 - [(5 - hydrazinyl - 4 - phenyl - 1,2,4 - triazol - 3 - yl)methyl] - 1H - indole [VI], this compound is synthesized by neucleophilic substitution reaction of 1,2,4 - triazole - 5 - thiol compound [V]a with excess of hydrazine hydrate in absolute ethanol as a solvent.b. Synthesis of 2 - {5 - [(1H - indol - 3 - yl) - propyl] - 4 - phenyl - 1,2,4 - triazol - 3 - yl} - thio - acetohydrazide[VIII]b, by the reaction of ester compounds[VII]b with excess of 80% hydrazine hydrate in ethanol under reflux.c. Synthesis of new Schiff bases[IX]a - d and [X]a - d by condensation reaction of primary amino compounds[VI] or [VIII]b with different aromatic aldehyde in absolute ethanol as a solvent.d. Synthesis of new N - acyl derivatives[XI]a - d and [XII]a - d by reaction of acetyl chloride with the synthesized Schiff bases[IX]a - d, [X] a - d in dry benzene.e. Synthesis of 1, 3 - diazetine derivatives[XIII]a - d and [XIV]a - d by addition reaction of compound[XI]a - d or [XII]a - d with sodium azide in dimethylformamid as a solvent at (55 - 60)0C temperature.2 - While the second part involved synthesis and characterization of novel thiazolidine - 4 - one compounds[XXI]a - d and [XXII]a - d by the following steps : Scheme(2).a. Synthesis of 2 - [5 - (2 - methyl - 1H - indol - 3 - yl) - 4H - 1,2,4 - triazol - yl] - thio - ethyl hydrazide[XVIII] by the reaction of ester compound[XVII] with excess of 80% hydrazine hydrate in ethanol under reflux.b. Synthesis of 2 - {5 - [(1H - indol - 3 - yl) - methylene] - 4 - phenyl - 1,2,4 - triazol - 3 - yl} - IXthio - ethylhydrazide[XVIII], by the reaction of ester compounds[XVII] with excess of hydrazine hydrate in ethanol under reflux. Also synthesize new Schiff bases [XIX]a - d and [XX]a - d by condensation reaction of acid hydrazide compounds [VIII]a or [XVIII] with different aromatic aldehyde in absolute ethanol as a solvent.c. Synthesis of new thiazolidine - 4 - one derivatives, [XXI]a - d and [XXII]a - d by refluxing equimolar amounts from Schiff bases[XIX]a - d and [XX]a - d with excess of thioglycolic acid in dry benzene.3. The third part involved synthesis and characterization of new series of thiazolidine - 4 - one [XXVII]a - c and [XXVIII]a - c by many steps reaction as follows : Scheme(3).a. Synthesis of new Schiff [XXIII]a,b, [XXIV]a,b by condensation reaction of acid hydrazide [III]a,b with two types of aromatic aldehyde in absolute ethanol.b. Synthesis of another type from thiazolidine - 4 - one derivatives [XXV]a, b and [XXVI]a, b from the reaction of Schiff bases [XXIII]a,b, [XXIV] a,b with excess of thioglycolic acid in dry benzene. The alkoxy derivatives of compounds [XXVII] and [XXVIII]; 2 - (4 - N - alkoxyphenyl) - 3 - (2 - methyl - 1H - indol - 3 - yl)amido - 1,3 - thiazolidine - 4 - one[XXVII]a - c and 2 - (4 - N - alkoxyphenyl) - 3 - (1H - indol - 3 - yl) acetamido - 1,3 - thiazolidine - 4 - one [XXVIII]a - c were synthesized by the reaction of terminal OH group of compound[XXV]a or [XXVI]a with different n - alkyl bromide in alkaline media.4 - The fourth part involved synthesis and characterization of amide derivatives of 1,3,4 - thiadiazole[XXXI]a - d, [XXXII]a - d and [XXXIII]a - d by the following steps : Scheme(4)a. Preparation of 2 - amino - 5 - (2 - methyl - 1H - indol - 3 - yl) - 1,3,4 - thiadiazole[XXIX] by cyclization reaction of 2 - (2 - methyl - 1H - indole - 3 - carbonyl) hydrazine carbo - thio amide [XV] in conc. H2SO4 under reflux followed by neutralized with liquid ammonia. While 2 - amino - 5 - [(1H - indol - 3 - yl)methyl] - 1,3,4 - thiadiazole[XXX]aand 2 - amino - 5 - [(1H - indol - 3 - yl)propyl] - 1,3,4 - thiadiazole[XXX]b synthesized by cyclization reaction under reflux of indole - 3 - acetic acid or indole - 3 - butric acid with thiosemicarbazide in the presence of phosphorous oxychloride.b. Synthesis of new amide derived from 2 - amino - 1,3,4 - thiadiazole [XXXI]a - d, [XXXII]a - d and [XXXIII]a - d from the reaction equimolar of suitable 2 - amino - 1,3,4 - thiadiazoles[XXIX] and [XXX]a,b with different acid chlorides in DMF and pyridine as accepter.5. The fifth part involved synthesis and characterization of new hydrazones [XXXVII]a - d and [XXXVIII]a - d. These compounds were synthesized according to the follows steps : Scheme(5)a. Synthesis and characterization of 1 - (2 - methyl - 1H - indole - 3 - yl) carbonyl - 3 - methyl - pyrazol - 5(4H) - one[XXXIV] and 1 - [(1H - indol - 3 - yl) ethanoyl or butanoyl] - 3 - methyl - pyrazol - 5(4H) - one [XXXV]a, b by heating under reflux a solution of equimolar from acid hydrazides[III]a - c with ethylacetoacetate in absolute ethanol.b. Synthesis and characterization of 1 - [4 - acetyl - (1H - indol - 3 - yl)ethanoyl or butanoyl] - 3 - methyl - pyrazol - 5 - one [XXXVI]a, b through reaction of pyrazolone derivatives[XXXV]a,b with acetyl chloride in 1,4 - dioxane in presence of calcium hydroxide.c. Synthesis and characterization of novel hydrazones [XXXVII]a - d and [XXXVIII]a - d by the reaction of 4 - acetyl - pyrazolone compounds[XXXVI]a, b with phenyl hydrazine or substituted phenyl hydrazine in ethanol.The synthesized compounds have been characterized by their melting points, elemental analysis (C.H.N) and by their spectral data, FTIR, 1HNMR and Mass spectroscopy (of some of theme).Study of the biological activity of some of the synthesized compounds against Gram - positive bacteria (Staphylococcus aureus) and Gram - negative bacteria (Escherichia coli). The results showed that most of the tested

تخليق وتشخيص ودراسة الخصائص التفلورية والمضادة لفايروس نقص المناعة المكتسبة لبعض مشتقات البركنينولون الجديدة == Synthesis, Characterization, Fluorescence Properties, Anti - Hiv Activity And Molecular Modeling Study of Some New Pregenolone Derivatives

Author name: رواء علاوي كاظم القريشي
Supervisor name: نجم عبود لعيبي المسعودي | نبيل عبد عبد الرضا
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: Arabic
University location: Qadisiyah
First pages:
Abstract: نظرا لما تتمتع به مركبات الازو من تطبيقات مهمة في كل من المجالين الاكاديمي والتطبيقي فقد تمحورت دراستنا على تحضير ستة ليكاندات ازو جديدة مشتقة من المركب 5,4 - ثنائي فنيل اميدازول ودراسة السلوك التناسقي لكل منها مع ستة ايونات فلزية هي Co(II) , Ni(II) , C | Azo compounds have important applications in both of academic and applied fields, Accordingly, our study based on the synthesis of azo compounds derived from 4,5 - diphenyl imidazole and characterization of these azo compounds with their metal complexese containing Co(II) , Ni(II) , Cu(II) , Zn(II), Cd(II) and Hg(II) ions. Mass Spectra of ligands and their complexes were supported their molecular formula, while H1NMR spectra of ligands agreed well with the suggested structures , The C.H.N. and Atomic absorption analysis showed a good agreement with the calculated values , The purity of ligands and their complexes were examined by TLC and the values of Rf were values measured.Electronic spectra of complexes showed a bathochromic shift comparing to ligands spectra as a result of the coordination between the metal ions and ligands. The concentrations that obeyed Beer - Lambert Law of the complexes were determined from calibration curves , Mole Ratio Method indicate a ratio (1 : 2) (Metal : ligand) for the complexes of (DPEPI) and (DPDED) while other complexes with other ligands show a ratio (1 : 1) (Metal : ligand).Satiability Constants of the complexes were calculated and found that the Stability constants of complexes of the first ligand (DPEPI) were ( 2.955×10 12) >(2.294× 1011 ) <(1.121×10 12 ) < (1.108 ×1011 ) varied in the arrangement as Co(II)< Ni(II) < Cu(II)> Zn(II) which agree with Irving - Williams Series. This arrangement was applied on the complexes of the other ligands. The Conductivity measurements of complexes showed non ionic character. Apparently the magnetic susceptibility values agree with their values of the octahedral high spin complexes for Co(II)) while the complexes of Zn(II), Cd(II), and Hg(II) were diamagnetic. IR Spectra of complexes showed obvious changes of the frequencies of ? (N=N) of azo group and ?(C=N) of heterocyclic imidazole ring as result of coordination with metal ions, While the frequencies of ?(C=N) of azomethine group did not show any significant change for complexes comparing to the ligands spectra ,New bands were appeared in the region (400 - 500) cm - 1 in the spectra of complexes that due to frequencies of ?(M - N) because of coordination process. From the previous results the purposed structures of the complexes can be summarized as shown in the following : Proposal structure of (DPEPI) Complexes Proposal structure of (DIDHP), (DIDMP),

تحضير ,تشخيص, دراسة فعالية مضادة للاكسدة ومضادة للسرطان لمعقدات الذهب (III) مع مركبات حلقية غير متجانسة == Synthesis ,Characterization ,Antioxidant And Anti - Cancer Activity Studies of Gold (III) Complexes With Heterocyclic Compounds

Author name: اية جمال عبد الحميد
Supervisor name: فراس عبد الله حسن
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: تضمن موضوع البحث تحضير مركبات حلقيه خماسية وسباعية غير متجانسة متنوعة،من خلال اربعة اجزاء هي : الجزء الاول : - تضمن هذا الجزء تحضير مركبات مشتقات 1, 3, 4 - اوكسادايزول من مركب (ثنائي اثيل مالونيت)، كما موضح بالمخطط (1).الجزء الثاني : - تضمن هذا الجزء تحض | This work involves synthesis of different five, and seven membered heterocyclic rings, and divided into four different parts and the reaction steps for each part are summarized as shown below.First part : This part involved the synthesis of 1,3,4 - Oxadiazoles derived from diethyl malonate.Scheme (1).Second part : This part involved the synthesis of Oxazepine , tetrazoles, and thiazolidinone,from 4,4' - ((((methylenebis(1,3,4 - oxadiazole - 5,2 - diyl))bis(3,1 - phenylene))bis(azanylylidene))bis(methanylylidene))bis(N,N - dimethylaniline).(Scheme 2).Third part : This part involved the synthesis of 1,1' - (1,4 - phenylene)bis(N - substitutedmethanimine) [C1 - 9] from terephthalaldehyde. (Scheme 3). Fourth part : This part involved the synthesis of 1,3,4 - Oxadiazoles derived from terephthalaldehyde and hydrazone carboxamide.In addition, this part deals with the evaluation of antibacterial activities of some of the synthesized compounds. These activities were determined in vitro using disc diffusion method against four pathogenic strains of bacteria (E.coli a, Pseudomonas, Bacillus, and Staphylococcus.), the results revealed that some of these compounds showed measurable activity. (Scheme 4).The liquid crystalline behaviors of the two series have been examined by means of hot - stage polarizing microscopy for the determination of phase transition temperatures and the type of mesophases. The prepared compounds are characterized through determining their melting points, colors physical properties) and (FT - IR, 1H - NMR,) spectroscopy, (C.H.N.S, DSC) analysis and checked by T.L.C.

نمط جديد للتحليل بالحقن الجرياني المستمر باستخدام نظام تشعيع متعدد القنوات مرتبة بهيئة مصفوفة خطية واثنان من الخلايا الشمسية لقياس التعكرية لتقدير الفصائل التحليلية ذات الاهمية : دراسة وتطبيق == New Mode of Cfi Analysis Using Multiple Channel Irradiation System In A Linear Array Arrangement With Twin Solar Cells For Turbidimetric Determination of Analytically Interesting Species : Study & Application

Author name: عمر اياد ياسين القيسي
Supervisor name: نغم شاكر تركي العوادي
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: الفصل الاول : يشمل الفصل الاول مقدمة عن تفاعلات الترسيب، مبادئها، ميكانيكية تكوين الرواسب، انواع الرواسب. وكما يتضمن الفصل الاول مقدمة عن الضوء والنظرية الكهرومغناطسية، وتداخل الضوء مع المادة (الانعكاس، الانكسار، النفاذية، الامتصاص). ناقش الفصل الاول بشكل

التقدير الطيفي لبعض المركبات العضوية المعوضة والمستحضرات الصيدلانية من خلال الاكسدة بايون السيريوم الرباعي باستخدام المحلل الطيفي الدقيق للتحليل بالحقن الجرياني المستمر (Ayah 3S BGR x3 -3D solar cell) == Spectrophotometric Determination of Some Substituted Organic Compounds And Pharmaceuticals Formulation Via Their Oxidation With Ce(IV) Ion Using Ayah 3SBGRx3 - 3D Solar Cell CFIA Microphotometer

Author name: مالك حسين علي العلوش العامري
Supervisor name: نغم شاكر تركي العوادي
General topic: Chemistry
Specific topic: Physical Chemistry
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: تم استخدام حسابات ميكانيك الكم التقريبية شبه التجريبية وفق نموذج الحساب PM3)) وحسابات ميكانيك الكم الاساسية التامة غير التقريبية وفق نظرية دوال الكثافة (DFT) وباسلوب B3LYP وعناصر قاعدة 6 - 311G لحساب جزيئة الفلرين التي امتلكت التماثل Ih مع وحدات بناءها (5 | Semi - empirical quantum mechanical methods (PM3) and Density Functional theory calculations (DFT/ B3LYP/ 6 - 311G) were executed to evaluate the fullerene molecule ,the internal coordinates (bond length and angles) and some physical and energetic properties.Calculations of the geometrical Parameters (bond lengths and bond angles), have shown that the (C=C) bond length is increased with increasing the size of the molecule that increased elasticity especially to fullerene to be like a ball. The (C - C) bond length is decreased with increasing the size of molecule, that means fullerene will be more stable than the other molecules.The energetic values (heat of formation) is found to be increased with the increasing of the size of molecule. The total energy is decreased with increasing size of molecule that means the stability will increase with the increasing of the size of unit construction of fullerene molecule , on the other hand , the energetic difference (E HOMO - LUMO) between the higher level of orbital and the lower level of orbital are decreased with the increasing of the size of molecule ' unit construction reaching to the fullerene molecule. So, this property will increase the significance of fullerene in the industrial and the electrical purposes.The vibrational modes frequencies with ( 3N - 6) whereas N is represented by number of molecule atoms which are evaluated with the absorption intensities of infrared frequencies. symmetrical and coordinated modes were discussed at the equilibrium geometric formation by using the programs MOPAC & Gaussian 05.It is worthy to say that it was not mentioned before that the complementary classification for the vibrated motion modes for such molecules , so our evaluations may considered unique. It is noted , as well , that CH stretching frequency has had fluctuations that means increasing and decreasing in the values of frequencies. In connected with the bending vibrated modes which taking place out of plane of the molecule are decreased with the increasing size of the unit constructions of molecule but it is increased only at the fullerene molecule. Conversely, the bending vibrated modes which are taken place in the plane of molecule are increased with the increasing the size of unit construction of molecule but are decreased at the fullerene molecule.The distribution of the electronic charges density on the atoms of unit construction of fullerene molecule were studied, the results shown the absence of the electronic charge on the atoms of Fullerene molecule and its concentrated at atoms of the outer circumferential edges C - Cc for the aromatic rings in its own unit construction. Semi - empirical methods (PM3) and Density Functional theory calculations (DFT/ B3LYP/ 6 - 311G) were carried out to evaluate the vibration frequencies and infra - red (IR) absorption intensities for equilibrium geometries of construction units of (6,0) zigzag (Mono (D6h), Di (D6d), Tri(D6h), Tetra (D6d)) ring layers SWCNTs and the internal coordinates ( bond length & angles ) at the equilibrium geometric formation symmetrically according to group theory were evaluated. The most important notes were axial bond length C - Ca which is decreased with the increasing of the tube length whether odd or even number of ring layers. The length of these mentioned axial bonds will be longer in the outer layers than the middle layers that means the increasing of stability of the tube with its length increasing , with the ability of replacing the external atoms of the tube because they are connected with longer and weaker bonds. The reverse was found with the circumferential bond lengths C - Cc was as they were increased with the increasing length of the tube whether the tube was odd or even in number of ring layers. Moreover , the lengths of these bonds are decreased in the middle side to the outer one for the odd and even ring layers. This will confirm the stability of the tube with its length increasing. The lengths of outer bonds C - H which are situated on the edges of the tube which were approximately fixed , with exception of the bond length of CH bonds in Mono ring layers which were longer because the large negative charge on carbon to which it is bonded and the large positive charge on it compared with the positive charge on hydrogen atoms of the multi - layers tubes. The heat of formation which was found to be increased with the increasing of the length of the tube , that means increasing of the stability and the aromatic properties , with the increasing of number of tube' layers. This property will increase the importance in the uses of these tubes for the industrial and electrical purposes as semi - conductors.The vibrational modes frequencies with 3N - 6 with the absorption intensities of infrared frequencies were evaluated and classified. These modes were discussed in symmetrical and coordinating manners at the equilibrium geometric formation, by using the programs of MOPAC and Gaussian 05 , with confirming on unavailability of bounded specification for such modes with 3N - 6 in the literature. We have a through our studies that the stretching vibration modes of symmetric and anti - symmetric Carbon - Carbon axial bond (C - Ca) increased with the increasing length of tube , and this will increase the physical properties for electrical conductivity with confirming on the significance of nanotube industrially. For the vibrational bending frequencies which are taking place in plane and out of plane of molecule surface as well as the vibrational stretching for odd number of ring layers (Mono and Tri) fluctuation will be happening in the relations , as all of them will be decreased with the increasing of tube ' length except (C - Caasym, C - Casym , ? CHsciss. , ? ringasym , ? ringsym and ? ringsym ) which be increased with the increasing the length of tube. The vibrational bending frequencies which are taking place in plane and out of plane of molecule surface for the even number of ring layers ( Di and Tetra layers ) will be decreased with the increasing of tube' length except (? CHsciss.) which is increased with the increasing of tube' length. Furthermore , all vibrational modes which are related to the puckering , breathing and bending movements of clockwise and anti - clockwise according to "group theory" were determined in accurate manner to which deformations are related , which are happened in the tubes , as a result of vibration, that may prevent the flow of electrons' movements and their transitions. The numerical values for the vibrational frequencies which are resulted from Semi - empirical methods (PM3) were acceptable in comparing with the strict calculations , hopping to achieve best values and to be close to the values obtained for the strict calculations (DFT) method to be suited with the basis and standards that are depended internationally. Some of these values were corrected by multiplied by constant scaling factors for such molecules. The results of scaling were good and very close to the experimental and calculated values.The distribution of charges' density on units of construction atoms of (6,0) zigzag nanotube SWCNTs also were studied. The results were consistent with the physical and experimental conductivity properties for such calculated tubes , as the intensity of the electronic charge was concentrated on the outer circumferential edges of atoms C - Cc for the aromatic molecules as well as for nanotubes with its disappearing form outer side towards the middle side of multi - ring layers ( Mono , Di , Tri and Tetra ).

تحضير وتشخيص عدد من معقدات البلاديوم (??) والبلاتين (II) مع مزيج من ليكاندات الثايويوريا او الحلقات غير المتجانسة الحاوية على الامين مع السكارين او الثايوسكارين == Synthesis And Characterization of Some Palladium (??) And Platinum(II) Mixed Ligand Complexes of Thiourea Or Heterocyclic Amine And Saccharin Or Thiosaccharine

Author name: نور عبد المجيد ضياف الدوري
Supervisor name: صبحي عطية محمود الجبوري | مظهر يونس محمد المهيدي
General topic: Chemistry
Specific topic: Organic Chemistry
Degree: Doctorate
Language: Arabic
University location: Salahaddin
First pages:
Abstract: تتناول هذه الاطروحة تحضير المركبات الحلقية غير المتجانسة ذات الحلقة الخماسية مثل معوضات الثايادايازول و3,2,1 - ترايازولين والثايازولدين - 4 - اون والحلقة الرباعية مثل الازتدين - 2 - اون والحلقة الثلاثية الاوكسازردين, فضلا عن تحضير الحلقة السداسية البرمدين | The thesis deals with hetero cyclic compounds with five member rings like thiadiazole substituted 1,2,3 - triazoline and thiazoldine - 4 - one, four member ring like azetidine - 2 - one and three member rings oxazirdine. Synthesis including six member ring compounds like pyrimidin - 2,4,6 - trione in addition to synthesis seven member ring compound like oxazepine are synthesized. In the present work 4 - bromo aniline is used as precursor for the synthesis of the required compound; the 2 - aminobenzothiazole - 6 - bromo (K1) is synthesized from the reaction of 4 - bromo aniline with potassium thiocyanate in presence of bromine, the later (K1) was reacted with ethyl chloroformate to give ethylcarbamate (K2),which is used for the synthesis of urea derivatives (K3 - 8).through (K2) reaction with substituted aniline. Pyrmidin - 2,4,6 - trione (K9 - 14) is synthesized from the reaction of malonic acid with urea derivatives in acetyl chloride.Schiff bases (K15 - 20) are prepared through the condensation of 2 - aminobenzothiazole with substituted benzyldehid. Seven member ring are synthesized by cyclaziation of Schiff bases (K15 - 20) by using malic anhydride in absolute ethanol to give 2 - aryl - 3 - N - 6 - bromobenzothiazole - 5 - 7 - dione oxazepene (K21 - 26). four member ring is prepared from the reaction of Schiff bases(K15 - 20) with chloro acetyl chloride in 1,4 - Dioxane in the presence of tri ethyl amine to give azetidine - 2 - one(K27 - 32). Thiazoldine - 4 - one(K33 - 38) is synthesized from the reaction of Schiff bases(K15 - 20) with thioglycolic acid in the presence of Zinc chloride. The Oxazirdine(K74 - 79) is also prepared from the reaction of Schiff bases(K15 - 20) with 3 - chloro per benzoic acid in pyridine. 2 - (2 - chloroacetamide) - 6 - bromobenzothiazole(K39) is prepared from the reaction of 2 - aminobenzothiazole - 6 - bromo (K1) with chloro acetyl chloride. The compound (K39) is used in the preparation of substituted aryl amino acetyl - 2 - amino - 6 - bromobenzothiazole (K40 - 46) through its reaction with substituted amine. The thiazoldine - 4 - one - 2 - imine (K47) is also synthesized from the reaction of compound (K39) with potassium thiocyanate. The thiazoldine - 4 - one - 2 - imine (K47) is reacted with substituted benzeldehyd to give 2 - (5 - (aryldin) - 2 - imino - 4 - oxo - thiazoldin - 3 - yl) 6 - bromobenzothiazole (K48 - 53).The 2 - (6 - bromobenzothiazole - 2 - ylimino) thiozoldine - 4 - one(K95) is prepared from the reaction of 2 - acetylamino - 6 - bromobenzothiazole(K39) with ammonium isothiocyanate in ethanol 96%. The thiazoldine - 4 - one(K95) is used in the preparation of 2 - (6 - bromobenzothiazole - 2 - ylimino) - 5 - (sub.Methyl) thiozoldine - 4 - one(K96 - 100) through its reaction with various amine and formaldehyde.The aminobenzothiazole (K1) is also used for the preparation of thiosemicarbazide (K54) by its reaction with carbon disulphide. The substituted 1,3,4 - thiadiazole (K55 - 60) is synthesized from the reaction of thiosemicarbazide (K54) with various of carboxylic acids in the presence of phosphorous oxychloride. The aminobenzothiazole (K1) is used in the preparation of aryl ( benzothiazole - 2 - ayl ) dithiocarbamate (K61 - 65) through its reaction with carbon disulphide and arylhalid or alkylhalid in ethanol.The 2 - azido - 6 - bromobenzothiazole (K66) is prepared from the reaction of sodium azide with diazonuim salt ( prepared from the reaction of benzothiazole (K1) with sodium nitrate , hydrochloric acid ). 1,2,3 - triazoline (K67 - 71) are synthesized through the reaction of 2 - azidobenzothiazole (K66) with various olefin in ethanol. The treatment of aminobenzothiazole (K1) with phenyl isothiocyanate gives (6 - bromobenzothiazole - 2 - yl) - 3 - phenylthiourea (K72) which is converted to (6 - bromobenzothiazole - 2 - yl) - 3 - phenyl - 2 - thioxydihydropermidine - 4 - 6 - one (K73) through its reaction with malonic acid in dry. Benzene. The 2 - hydrazinobenzothiazole (K80) is prepared from the reaction of 2 - aminobenzothiazole (K1) with a mixture from hydrazine hydrate and hydrochloric acid in ethylene glycol. Pyrazoline compounds (87 - 92) are synthesized from the reaction of chalcons (K81 - 86) ( which are prepared from the condensation of substituted benzaldehyde with acetophenone in a base medium ) with hydrazino (K80). The hydrazino (K80) is used in the preparation of 2 - amino( - 6 - bromobenzothiazole)isoandole - 1,3 - diaone (K93) and 1 - (2 - amino - 6 - bromobenzothiazole)pyrroline - 2,5 - di - one (K94) through its reaction with phathalic anhydride and malic anhydride in ethanol. For furthur work, the preparation of Schiff bases (K101 - 110) carried out. from the condensation of substituted benzaldehyde with hydrazino (K80) in the presence of glacial acetic acid in ethanol. The 3 - ( - 6 - bromobenzothiazole - 2 - ylamino) - 2 - (sub.aryl) - 5,7 - di - one oxazipene (K111 - 120) are synthesized by cyclazition of Schiff bases (K101 - 110) by using malic anhydride in methanol. Schiff bases (K101 - 110) are also used in preparation of 1 - ( - 6 - bromobenzothiazole - 2 - ylamino) - 4 - (sub.aryl) - 3 - chloro - 2 - oxo - zetidine - 2 - one (K121 - 130) through its rection with chloro acetyl chloride in presence of tri ethyl amine in 1,4 - Dioxan. The 3 - (6 - bromobenzothioazol - 2 - ylamino) - 2 - (substituted aryl)thiozoldin - 4 - one (K130 - 140) is prepared from the reaction of thioglycolic acid with Schiff bases (K101 - 110) in presence of zinc chloride in dry. Benzene. In order to show the antibacterial activity of prepared compounds (k11,k23,k41,k56,k61,k62,k89,k97,k112,k118,k126,k137,k139) are evaluated against four types of common bacteria (Bacillus subtillis, Staphylococcus aureus, Eschershia coli, Klebsiella peneuomina). The result of biological study are compared with standered antibiotic (Ciprofloxacine & Gentamycin). The structure of the synthesized compound are confirmed by I.R, 1H - NMR & 13C - NMR spectra and Some chemical physical data.

دراسة بعض المتغيرات الكيموحيوية على مرضى ضغط الدم

Author name: منال عدنان ابراهيم
Supervisor name: نزار احمد ناجي
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: Arabic
University location: Salahaddin
First pages:
Abstract: يتضمن البحث تحضير مشتقات جديدة للقاعدة النتروجينية البيورينية (ثيوفلين) باضافة مجموعة ازو (Azo group) الى هذه القاعدة حيث تتصل بالطرف الاخر لمجموعة الازو الحلقية حلقة بنزين معوضة بمجاميع مختلفة مثل (SO3H , Br , NO2) وقد حضرت اربعة مشتقات للثيوفيلين1 - SA | This study include synthesis of new derivatives of nitrogen bases purin (theophylline) by adding azo group to these Bases where connecting in the other terminal with Banzen ring substituted by different group like (NO3, Br,...) Four derivatives of the theophylline where these are SAT , BAT , 4NAT , 3NAT these derivatives were used as ligand because of is abitity to from helating complex , these derivatives were reacted with eight metal ions these are (Fe2+, Co2+, Ni2+, Cu2+, Zn2+, La3+, Ce3+) these complex were characterized by many methods as molarratio, measuring of electrical conductivity electronic spectra , which helped us to find the chemical structure of those complex this study also found that ratio of ligand metal was 2 : 1 this study also include the study of biological effect for these ligand and complexes on four deferent pathogenic species (staphylococcus aureus, streptococcus viridans ) ,(protens vulgaris, pseudomonas aeruginosa ) the two first species are gram positive while the other are gram negative , finally (by using disk diffusion method) it was found that these compounds show different activity of inhibition on other growth of the Becteria.

تطبيقات طريقة استخلاص سائل - سائل للفصل والتقدير الطيفي لبعض العناصر الانتقالية بواسطة معقدات عضوية جديدة == Applcations of Liquid - Liqid Extraction Method For Separation And Spectrophotometric Determiination To Some Transition Metal Elements By New Organic Reagents

Author name: احمد ابراهيم حمزة
Supervisor name: شوكت كاظم جواد
General topic: Chemistry
Specific topic: Biochemistry
Degree: Doctorate
Language: Arabic
University location: Najaf
First pages:
Abstract: اجريت هذه الدراسة لمعرفة تاثير مرض ارتفاع ضغط الدم على بعض المتغيرات الكيموحيوية في الدم, ومقارنتها مع القيم الطبيعية (مجاميع السيطرة) والبالغ عددهم (125) (47 اناث و72 ذكور) والذين تراوحت اعمارهم بين (21 - 70) سنة حيث تضمن البحث : دراسة 115 حالة مرضية للاش | The present study was carried out to determine the effect of hypertension on some biochemical parameters in the blood compared to that of normal values of healthy subjects in healthy control group(125) (47 females and 72 males) Their ages ranged between(21 - 70) yearsThe study included : - 1 - seventy hypertensive patients(30 females and 40 males)Their ages ranged between (30 - 80) years the following biochemical parameters were included : (Cho, TG, HDL, LDL, VLDL, GOT, GPT, SOD MDA, HbA1C ,LDH, Metall oendopeptidase , leptin )for both hypertensive patients and health subjects as a control. Results of this study have shown a significant increase(p?0.05) in the concentration of cholesterol, triglyceride ,LDL,VLDL compared with control group while high density lipoprotein showed a significant decrease (p?0.05) compared with control groupThe estimation of LDL/HDL ratio showed a significant decrease (p?0.05) compared to that of healthy subjects The study also included the effect of hypertension duration on BMI and age in relation to the concentration of (Cho, TG ,LDL,VLDL,HDL)The study showed increase in the concentrations of (Cho, TG ,LDL,VLDL) while a decrease in the concentrations of high density lipoprotein for all patients compared with that of healthy subjects (control group).A clinical study of Metallo endopeptidase on the serum of healthy and hypertensive patients was carried which has been shown that the activity of this enzyme in healthy subjects does not affect by sex, age, and smoking while there is significant increase in the activity of Metallo endopeptidase in the serum of the hypertensive patients for both sexes at different ages compared with that of control group while there was an increase in the activity of Metallo endopeptidase in relation to the duration of disease the result also demonstrated a significant increase in the activity of lactate dehydrogenase in hypertensive patients compared with that of control group.ALT and AST enzyme levels have been estimation in this study which showed a significant increase in the level of AST in hypertensive patients for both normal weight and overweight compared with that of control group, while ALT level showed no significant difference in hypertensive patients for both normal weight and overweight compared with that of control groupAs for Leptin the study has showed a significant increase in the concentrations of leptin hormone in control group of healthy subject (over weight BMI?25) compared with normal weight(BMI?25) for the same group. the concentration of leptin in all hypertensive patients showed an increase level in relation to age &BMIThis study also included the estimation of SOD and MDA in both hypertensive patients and healthy subjects (control group).It showed a significant decrease in the activity of SOD as the duration increases and there was a significant increase in the level of MDA(P?0.05)in hypertensive patients compared healthy group.Finally the level of (HbA1C) was also studied which no significant difference in hypertensive patients compared with that of control group, while there was a signi

دراسات كيمياء الكم لمركبات الروثينيوم العضوية الفلزية == Quantum Chemical Studies of Ruthenium Organometallic Compounds

Author name: دريد توفيق عريبي الكنبي
Supervisor name: محسن عبود محسن العبادي | حسين جاسم محمد
General topic: Chemistry
Specific topic: Chemistry
Degree: Doctorate
Language: English
University location: Najaf
First pages:
Abstract: There are a wide variety of polyphenolic compounds named flavonids. These are extensively distributed in plants, and they are considered to be dietary antioxidants. They occur naturally in broad range of vegetables, fruits, and primarily recognized as the pigments.Many flavonoids have a metallic ion complexation capacity. The study of this capacity is important because it can be used in producing nutritional supplements, medicine, and heavy metal detoxification.Chelation therapy is the use of chelating agents (complexing agents) to detoxify poisonous metal such as mercury, arsenic, and lead by converting them to chemically inert form that can be excreted without further interaction with the body.Lead is considered as one of the most hazards and cumulative environmental pollutants that affect all biological system through exposure from air, water and food sources. It is toxic heavy metals which are known to induce a broad range of physiological, biochemical and behavioral dysfunction in humans. Because of its perverseness in the environment, lead poisoning still remains an important health problem.The polarographic measurements were carried out using differential pulse polarography (DPP), at hanging mercury drop electrode (HMDE) at the optimal conditions for flavonoids which were 1M HCl for Quercetin, Rutin, and Hespertin and 0.01M NaOH for chrysin as a supporting electrolyte.A well - defined two electron reversible reduction and diffusion controlled one wave for these flavonoide were observed, a linear relationship between concentration and diffusion current (id) was obtained with the value of correlation coefficient (r2) near to one, this obey Ilkovic equation. The values of n; the number of electrons transferred in the reduction process were obtained from the slop of the straight line corresponding to E vs. log i/id - i.Addition of flavonoides to a solution of Pb (II) ion, show the appearance of a new peak in a more negative potential than Pb (II) peak, with the gradual decrease in id of Pb (II) ion which suggests the complex formation between them.The stoichiometry and the stability constant of Pb (II) complex with flavonoids were calculated by Lingane equation; a plot of ?Ep vs. log [L] give a straight line, the slope of the line allows the determination of the coordination number (p), and the stability constant were determined from the intercept, the stoichiometry of these complexes were (1 : 1) with a stability constant of : Pb - Quercetine (5.5*107) ? Pb - Rutine (1.3*107) ? Pb - Hespertine (4*106) ? Pb - Chrysin (5.4*104)These measurements also includes the determination of the kinetic parameter of the electrode reaction (Kth, ?n) and the thermodynamic parameters such as ?H, ?G, and ?S.The spectrophotometric measurements were carried out in 50% methanol/water for Quercetin and Rutin, 30% methanol/water for Hespertin and in phosphate buffer of pH - 7 for Chrysin.The electronic spectrum of free flavonoides in methanol solution was mainly characterized by an important absorption band at ? 370 nm (band I) and a second one located at ? 256 nm (band II). Upon addition of lead (II) to the flavonoids solution significant changes are observed in the electronic spectra, a bathochromic shift in band (I) to the extent of ? 40 nm and a shift in band (II) to the extent of ? 7 nm, the change in ?max and the change in the intensities of the bands were due to the coordination between flavonoids molecules and Pb (II) ion.The stoichiometry of the formed complexes were investigated by the method of continuous variation and it were found (1 : 1), the stability constant were calculated also and were found to be in the order of ? 105 to 106.Thermodynamic parameters and kinetic studies were also determined which indicates a second order interaction between lead (II) and these flavonoides.Spectroscopic measurements for (EDTA) Complexation with lead (II) were carried out in order to compare its stability constant with that obtained for flavonoides complexes, due to its application in the treatment of metal poisoning.Stability constant of (EDTA) with Pb (II) complex were in the order of 108 which is much more efficient than flavonoides.

تعيين بعض المضادات الحيويه بطرائق الامتصاص الذري وكروماتوغرافيا السائل ذات الاداء العالي والمطيافيه الجزيئيه عن طريق تكوين معقدات مع ايونات الذهب والزئبق == Atomic Absorption, Hplc And Spectrophotometric Determination Of Some Antibiotics In Pharmaceutical Preparations Via Complexes Formation With Au (Iii) And Hg (Ii) Ions

Author name: عباس شبيب حسن الكاظمي
Supervisor name: احلام جميل عبد الغني | هادي حسن جاسم
General topic: Chemistry
Specific topic: Analytical Chemistry
Degree: Doctorate
Language: English
University location: Baghdad
First pages:

تحضير وتشخيص مشتقات جديدة للكوينولين - 2 - اون المعوضة على ذرة النايتروجين وتقييم فعاليتها البايولوجية == Synthesis And Characterization Of New N - Substituted Quinoline - 2 - One Derivatives And Evaluation Of Their Biological Activity

Author name: لمى سامي احمد
Supervisor name: رضا ابراهيم حسين البياتي | محمد رفعت احمد
General topic: Chemistry
Specific topic: Organic Chemistry
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
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