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تحضير وتشخيص بعض مركبات ازو - ازوميثين واستخدامها في استخلاص ايون الكاديميوم الثنائي بطريقة استخلاص نقطة الغيمة == Synthesis and characterization of some Azo - Azomethine compounds and using them in could - point extraction of Cadmium Ion

Author name: ميعاد نكاد عوض
Supervisor name: ساهر عبد الرضا علي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar

تحضير وتشخيص مشتقات جديدة ين 4,3,1 - اوكسادايازول و 4,2,1 ترايازول ومعقداتها مع بعض ايونات العناصر الانتقالية == Preparation and Characterization of new Derivatives of 1,3,4 - Oxadiazol and 1,2,4 - Triazole and its complexities with some transition metal ions

Author name: امنة نعيم هليل الركابي
Supervisor name: ابراهيم عبود فليفل
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar

تحضير وتشخيص ودراسة بايولوجية لمشتقات جديدة من 4,2,1 - ترايازول ومعقداتها مع بعض العناصر الانتقالية == Preparation, Characterization and biological study of some new 1,2,4 - Triazole derivatives and theirs complexes with some transition metals.

Author name: احمد كامل عجيل الزيدي
Supervisor name: ابراهيم عبود فليفل
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
Abstract: he work listed by this thesis covers the preparation and characterization ofsome new derivatives of 1,2,4- Triazole as ligands which are : | 1-N : ( 2-ethyl-5-{[(3-phenyl-5-sulfanyl-4H-1,2,4-triazol-4-yl)imino]methyl}benzene-1,4-diol). (L1)2-4-({2-[(4-methylphenyl)amino]ethylidene}amino)-5-phenyl-4H-1,2,4-triazole-3-thiol (L2)3-5-methyl-4-{[1-(5-methylfuran-2-yl)ethylidene]amino}-4H-1,2,4-triazole-3-thiol (L3) | Those ligands were used to prepare some complexes such as L1,L2,L3with the chlorides of transition metal(FeCl3.6H2O,COCl3. 6H2O,CrCl3.6H2O,CuCl2.6H2O,NiCl2.6H2O)To characterize the structure of prepared ligands and their complexes, | elemental analysis (C.H.N),Infrared Spectroscopy (IR), NuclearMagnetic Resonance Spectroscopy(1H-NMR),Mass Spectra,Magneticsensitivity and Molar conductivity techniques were applied . The resultsshowed that ; | 1- The complexes of [Fe(III) , Co(III) , Cr(III)] for all ligands haveshown octahedral configuration. | 2- Complexes of [Ni(II) , Cu(II)] with all ligands have shown square | planer configuration.Testing the biological activity for ligands and their complexes by using spread method and measurement inhibition zone by using (DMSO) as asolvent showed a positivity results; By the appear laeg inhibition zonesagainst E-coli and S. aureas species of bacteria.

تحضير وتشخيص ودراسة بايولوجية لبعض مركبات ثنائية الازو الجديدة ومعقداتها واستخدامها كوثبطات لتاكل سبيكة الفولار الكاربوني في الوسط الحامضي == Synthesis,Characterization and Biological activity Study of Some Bis - Azo Dyes and their Complexes and the use of Bis - Azo dyes as Corrosion Inhibitors for Low Carbon - Steel in acidic media

Author name: اسراء عبد الكاظم جاسم الشمري
Supervisor name: ساجد حسن كسار | حسام محمد كريدي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
Abstract: As it used for dyes (A1,A3) P-Phenylenediamine ,while using for dyes (A2,A4) O Phenylenediamine. | here is X for dyes (A1,A2) 3-ethoxy salicylaldehyde ,while representing for | dyes 3-methoxy salicylaldehyde. | he prepared copmpounds were identified by FT-IR spectroscopy, CHN analysis, 1H-NMR spectroscopy and GC-Mass spectroscopy.Also, determination of melting pointsWhere,XIn the recent study, four azo dyes compounds were prepared (A1-A4) and tested as The inhibition efficiency of the synthesized compounds was studied , using | weight loss method in acidic solution by corrosion rate determination for | carbon steel without and with different concentratins | ) 1 , 5 , 1 , 5 ( M | of inhibitor at different immersion times (1-5) hrs ,303K and static condition | .The inhibition efficiency of synthesized compounds was calculated ,the | optimum concentration ( 5 M ) and immersion time (5 hrs) were | determined at the same conditions.The compounds have agood corrosion | inhibition with efficiency percentage of (86.47-88.26%) for azo dyes. | The effect of temperature variation on the corrosion rate for different | concentrations (1 -5 M) of the prepared compounds was studied | by using weight loss method at four temperature degrees (303, 313,323 and | 333)K and (1-5) hrs. | The experimental results of temperature effect indicated the following : | 1-The rate of corrosion inhibitors increased with the rise of temperature, while | the corrosion rate decreased with increasing of inhibitor concentration at the | certain temperature.For example ,the corrosion rate for carbon steel in the | presence of A2 inhibitor increased from 39.22mpy at 303K to 464.75mpy at | 333K.while the corrosion rate decreased from 70.50mpy at concentration of | 1 M to 39.22 mpy at concentration of 5 M at constant | temperature of 303K. | 2-All inhibitors had high inhibition efficiency in reducing the corrosion rate.The | inhibition efficiency was decreased by increasing the temperature ,for example | inhibition efficiency for A2 inhibitor was decreased from 88.26% at 303K to | 85.44% at 333K. | 3-The adsorption of the molecules on the metal surface obey Langmuir | isotherm.The adsorption constant and free energy of adsorption were | calculated for the studied inhibitors.The results showed that the adsorption | constants were decreased with increasing the temperature and the negative | value of free energy indicated that the adsorption process is spontaneous. | 4-Thermodynamic functions H and S and the activation energy Ea were | determined.The results indicated that the activation energy for acidic solution | without inhibitor (16.21 KJmol-1 )was less than of the activation energy value | with the presence of inhibitor s, (17.08-31.07 KJmol-1 ) for azo dyes .The | positive value of enthalpy indicated that the metal dissolution process is | endothermic , while the negative value of entropy reflected the reducing in the | entropy value and formation stable layer on the metal surface. | Electrochemical method (Tafel plot) was used to evaluate the inhibition | efficiency for the azo compounds using carbon steel corrosion in 0.5M HCl | solution. The percentages of inhibition efficiency were 86.84%, 93.68%, 86.70 | and 93.06% for the inhibitors A1, A2, A3 and A4, respectively, at 303K and | concentration of 5 x 10-3M. Tafel plot results indicated that the prepared azo | dyes compounds are the doublet inhibitors type. | Studying of the growth inhibition against three types of pathogenic bacteria | namely for some pigments lecture(A1,A2) and their Nickel(II) complexes by | using diffusion method and measurement inhibition zone by using (DMSO) as a | solvent , using in this study three types from bacterial two its Gram negative | bacterial strains, Escherichia coli, Pseudomonas Aeruginosa and the other is Gram positive bacterial strains , Staphylococcus aureus , We notice that the biological activity against this bacterial showed a positivity results. | Ciprofloxacin were used as standard bactericide and compared inhibition this | bacterial with Ciprofloxacin.corrosion inhibitors in acidic medium ,0.5M HCl. These compounds have general chemical structure :

تحضير وتشخيص ودراسة الفعالية البايولوجية لمشتقات جديدة من 4.3.1 اوكسادايازول ومعقداتها مع بعض العناصر الانتقالية == Preparation , characterization and biological activity of a new1,3,4 - oxadiazole derivatives and some of their transition metal complexes

Author name: ايمان حسين شويل التميمي
Supervisor name: ابراهيم عبود فليفل | احمد حسن محمد
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
Abstract: The work described in this thesis is mainly concerned with preparation and characterization of three ligands (L1-L3) derived from 1,3,4-Oxadiazole .The study deals with reaction of these ligands with transition metal salts as (CrCl3.6H2O , CoCl2.6H2O , NiCl2.6H2O , CuCl2.2H2O) .The ligands and their complexes were characterized by the elemental analysis (C,H,N), Infrared spectroscopy (IR) , Proton Nuclear Magnetic Resonance Spectroscopy (1HNMR), Mass spectra and molar conductivity. However, the ligands and some of their were studied by using hyperchem7.5 program in order to know their geometry and proving their shapes and hypridizaion which were notice the chromium complexes is octahedral (oh), the hypridization is d2sp3 with the three ligands while the shapes of the complexes (cobalt(II), Nickel(II), Cupper (II) ) is four coor-dinated is square planar and the hypridizaion is sp3. | Antibacterial activity was carried out against Escherichia coli, Staphylococcus aureus, Streptococcus pyogenes and Klepsiella pneumonia, and with test compounds at four concentrations of (5, 2.5, 1.25, 0.625mg/ml). Azithromycin and Cefoaxime were the standard drugs utilize. Some of these compounds showed good efficacy, while others ranged from medium to small. | The hemolysis activity of the compounds was tested at different concentrations (5, 2.5, 1.25, 0.625mg/ml) and the results showed high percentage of hemolysis for all these compounds and these gave a conclusion about the contraindication use of these compounds in vivo .

تحضير وتشخيص قواعد شف ومعقداتها المشتقة من 4 - امينوانتيبايرين واستخدامها في استخلاص ايون النيكل الثنائي == Preparation and Characterization of Schiff Bases and their Complexes Derived from 4 - Aminoantipyrine and using them in the Extraction of Nickel (II) Ion

Author name: اسراء جرجيس نعمة
Supervisor name: ساهر عبد الرضا علي | حيدر عباس مهدي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
Abstract: The study includs the preparation and charazchtion of three new compounds of the schiff bases are : | 1- L1 is prepared from the condensation of 4-amino antipyrine with Penzaal acetone . | 4,4'-((1Z,1'E)-(1-phenylbutdiylidene)bis(azanylylidene))bis (1,5-dimethyl-2-phenyl-1Hpyrazol-(2H)-one)3 | 2- L2 is prepared from the condensation of4-amino antipyrine with Asetayl acetone | 4,4'-((1Z,1'E)-pentane-2,4-diylidenebis(azanylylidene))bis(1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)- one | 3- L3 is prepared from the condensation 4-amino antipyrine with Slsldehid as a first step then it is is reactance output with 3.4-di amino toluene . | 2,2'-((1Z,1'E)-( (3E,3'E)-3,3'((4-methyl-1,2-phenylene)bis(azanylylidene)) bis(1,5-dimethyl-2-phenyl-2,3-dihydro-1H-pyrazole-4-yl-3- ylidene))bis(azanylyidene))bis(methanylylidene))diphenol | The ligands were characterized by using Elemental Analysis (C.H.N), Infrared Spectroscopy (FT-IR) ,Uv-visible Spectroscopy , Nuclear Magnetic Resonance Spectroscopy (1H-NMR) , Mass Spectra . It is appeared that prepearing ligands are tetra chelatingagents kind (N2O2) for the ligands L1 and L2 and kind (N4) for the ligand L3. The complexed are prepeared from reaction the prepearing ligands with some transitional elements (Ni+2 , Co+2 , Cu+2) and the ligends and their complexes were characterized by methods of spectral analysis,Uv-visible Spectroscopy,Infrared Spectroscopy (FT-IR) , Mass Spectra and the Molar Electrical Conductivity .And from the result that we know the complexes are octahedral and their general formula [M(L) Cl2] , whereas M = Ni+2 , Co+2, Cu+2 . The study includs an extraction of nickel(II) ion from its aqueous solutions using solvent extraction technique by employing the reagent L3. The optimum extraction conditions are studied to obtain a better distribution ratio of values for (D) to reach the best percent extrected (%E) to extract nickel (II) ion . It is noted that the best values of distribution ratio (D) and the best percent extrected (% E) extracting nickel ion duo with the reagent L3 at the time of shake (15) minutes .The best extraction to nickel(II) ion with reagent L3 at temperature (25C°). As it turns out from this study that the best acidic function nickel(II) ion extraction in the aqueous phase with reagent L3 in the organic phase | when the (PH=9),also the study shows that the best values of distribution ratio (D) and the percent extrected (% E) for nickel(II) ion extraction when its constriction was (120 μg/ml) | (4.5×10-4 M ).The reagent L3 concentration (1× 10-4 M) . Chloroform was the best organic solvent for an extraction process for nickel(II) ion with reagent L3.The reagent L3 also is used for extraction Ni+2 from water of the Euphrates River City of Nasiriyah and the distribution ratio (D) =4.81 and the precent of extrected =%82 as it becomes out the reagent has high efficiency for extrected from the sample .

تحضير وتشخيص بعض مركبات النايترون الجديدة ودراسة الفعالية البايولوجية لها == SYNTHESIS And characterization OF Some new Nitrones Compound and The study of biological effectiveness

Author name: زهراء حميد كامل
Supervisor name: ماجد حمود مزيعل
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
Abstract: This study was included the preparation of a series of compounds heterogeneous Nitrones. Novel compounds were resulting from the reaction between azo compounds and hydroxylamine compounds through several steps. | the first step was synthesis of a new azo compounds for 2-aminopyridine includes (2a, 2b, 2c, 2d) by configuration the diazonium salt, which in turn enters the reaction of duplication with these aldehydes (2-nitro benzaldehyde, 4-dimethylamino benzaldehyde, 4-chloro benzaldehyde and 4-hydroxy benzaldehyde) respectively. | The second step was included the preparation of hydroxylamine compounds, (N-phenyl hydroxylamine and N-p-toluidine hydroxylamine) were reduced depending on the methods published in the literature. | The third step included the reaction between N-phenyl hydroxyl amine and azo compounds to gave nitrones compounds first set (3a, 3b, 3c, 3d) respectively. | Also we prepare nitrones compounds by the reaction between azo compounds with N-p-toluidine hydroxylamine to give Nitrones compounds second set (3e, 3f, 3g, 3h). | It has been identified the both novel azo-aldehydes and nitrones compounds by using infrared spectroscopy (FT-IR), spectrum NMR proton (1H-NMR), spectrum NMR carbon (13C-NMR) and mass spectrometry (Mass Spectra ) as well as we measured the Melting point for the preparing compounds. | We also Study the effectiveness of biological compounds of the prepared compounds inhibited the growth of some bacteria positive and negative gram, it has shown some compounds to be effective in killing or inhibition of these germs. | next table shows the compounds prepared in this study.

تحضير وتشخيص بعض مركبات N - Oxide جديدة ودراسة فعاليتها الحيوية == Synthesis and characterization of some novel N - Oxides and Study their Biological activities

Author name: نور عبد الخضر سلمان الاميري
Supervisor name: ماجد حمود الصافي | محمد عجه عوده
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
Abstract: In this study, we prepared a series of nitrones compounds resulting from the interaction of azo dyes prepared which contain Carbonyl edge with hydroxylamine compound . | It was prepared a series compounds of azo dyes (A1, A2, A4, A5) have been prepared by the reaction between 2- amino pyrimidine with diazonium salts which contain benzaldehyde derivatives(4-hydroxy benzaldehyde, 4- chloro benzaldehyde, 4-dimethylamino benzaldeyde, 2- nitro benzaldehde). While the compound A3 was prepared by the reaction between 6-amino-2-mercaptopyrimidin-4-ol with 4-hydroxy benzaldehyde.It was also prepared two groups of Nitrones, the first | group includes the compounds (B1, B2, B3, B4, B5) resulting by the reaction between azo dyes prepared (A4, A2, A5, A1, A3) respectively with N-phenyl hydroxylamine. | On the other hand the second group includes the compounds( C1, C2, C3) resulting by the reaction between azo dyes (A4, A2, A1) respectively with NParatolyl hydroxyl amine Those compounds have been confirmed the authenticity | of the molecular structures of the compounds prepared | using the TLC, infrared spectroscopy and 1H-NMR | spectrum and 13C-NMR spectrum. | It has also been study the toxicity by the calculation of the median lethal dose LD50 of one of the prepared Nitrone compound B1 on laboratory rats , the result was that the prepared compound was non toxic at the used doses ( 34.2-136.8 ) . | We also study the biological activity of the prepared compounds ( Alaldehydes and Nitrones ) by observing its effect on negative and positive bacteria of gram dye

تحوير فجوة طاقة ثاني اوكسيد التيتانيوم بواسطة تفاعلات الحالة الصلبة مع صوديوم بوروهيدريد والمنيوم ليثيوم هيدريد وتحديد فعالية التحفيز الضوئي == Modifying The Band Gap of Nano Titanium Dioxide By Solid State Reactions With Aluminum Lithium Hydride and Sodium Borohydride and Determining Their Photocatalytic Activity

Author name: سراج علي رحيم
Supervisor name: محسن عريبي الدخيلي | ابراهيم عبود فليفل
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: English
University location: Dhi Qar
Abstract: This study includes preparation of nanoparticles of titanium dioxide using sol-gel method and then, the band gap was modified by solid state reaction with (AlLiH4،NaBH4) reductive compounds. Modification reduced the band gap separating | energy levels between valance band (VB) and conduction band (CB), therefor; facilitating the transfer of excited electrons from (VB) to (CB). Absorption of the energy from incident photons having the same or larger energy than the energy of the | band gap promote the formation of the couple (electron - hole) . The resulting (e--h+) couple acts to produce (OH.) radicals. OH. radicals hav a high capability to destroy organic pollutants that adsorbed on surface of the photocatalytic TiO2. | The optical properties measured using UV-visible spectrophotometer (Absorbance (A), energy band gap (Eg) and absorption coefficient ( α ) . TiO2 and TiO2- solid state reaction showed clear blue shift of the absorption band gap which were (2.8ev, 2.7ev, 2.25ev, 2.0ev) to )TiO2- NaBH4(550 ) ,TiO2-NaBH4 (750 ) , TiO2-AlLiH4 (500 ) and TiO2 -AlLiH4 (750 )) respectively. The structure of prepared TiO2 nanopowders were identified using XRD, particle size distribution varied appreciably in comparison with crystallite size (D) calculated from Sheerer formula which was in a good accordant compared with ASTM results , the particle size and their distribution were characterized using (AFM) . To the surface forms and compositions diameters of nanoparticles)SEM) was implemented . The energy dispersive X-ray (EDX) microanalysis was utilized to investigate the chemical composition of the whole samples. | Photocatalytic reaction was studied by using UV-Vis spectrophotometry. | In photocatalytic reaction the effect of the catalyst on photocatalytic rate of decomposition of methylene blue dye through the use of catalyst TiO2 and TiO2- solid state reaction (TiO2 - NaBH4 (550 ,750 )) and (TiO2 - AlLiH4 (500 ,750 )) . Using constant weight of the catalyst and dye. The most effective weight was found (1*10-4 M). At best weight the influence of many factors on rate of decomposition of dye were studied the impact of change pH varies (4.5, 7.1 and 9.4) found that the highest percentage in the decomposition of the MB was in the acidic media than in neutral and then alkaline. The effect of temperature variation from (20, 30, 40ºC) and found that increased rate of decomposition with increasing the temperature of the MB. Activation energy (Ea) for each reaction was calculated by using the equation of Arrhenius equation between (5.73-11.31) kJ mol-1 . | A series of dark reactions with absorbance measurement by UV-Vis spectrophotometry, within different periods of time with the change of pH and temperature. The results indicate that no degradation of the methylene blue dye although all the factors affecting in photocatalytic present except UV-light .

تحضير بعض الفورمازنات والثايازوليدينونات الجديدة ودراسة فعالية بعض المركبات المحضرة في خفض سكر الدم

Author name: هبة محمد داغر راشد
Supervisor name: حيدر عباس مهدي | كريم سالم عباس
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: English
University location: Dhi Qar
First pages:
Abstract: The thesis consists of three chapters. The first chapter is concerned with the introduction described the chemistry of Schiff bases , formazans and thiazolidinones compounds including importance , applications , synthesis and literature reviews.The second chapter describes the chemicals and solvents which were used in the synthesis of the new Schiff bases, formazans and thiazolidinones derivatives, physical measurements , synthesis methods of compounds and evaluation of anti - hyperglycemic activity. The formazans compounds[4a - 4h] were prepared by reacting diazonium salts amines[3a - 3c] with the appropriate Schiff bases[2a - 2h].Schiff bases themselves are synthesized by the condensation of different primary amines with various aromaticaldehydes. The thiazolidinones derivatives[5c,5e,5i,5j,5k] are synthesized by condensing thioglycolic acid with various Schiff bases[2a - 2h]. All the structures prepared [2a - 2k] , [4a - 4h] and [2c, 2e ,2i ,2j , 2k] were shown in scheme(1), and characterized on the basis of the spectral data : IR, Mass, 1H and 13C NMR. The third chapter deals with , the results and discussion. The IR spectra show an important absorption band at (1558 - 1689)cm - 1 attributed to azomethine (C=N) for Schiff bases, the IR spectra showed important absorption band at (1681 - 1597 )cm - 1 attributed to azomethine (C=N) and (1465 - 1558) cm - 1 to ( - N=N - ) for formazans derivatives. Also, the IR spectra show an important absorption band at (1689 - 1658)cm - 1 attributed to the thiazolidinones ring . The 1H - NMR spectra of formazans show aromatic protons at the range (7.07 - 8.49 )ppm and pyridyl protons as downfield signal at (8.22 - 9.15 ) hydrazide signal at 11 ppm. The 1H - NMR of thiazolidinones exhibit new signals attributed to - CH2 and - CH of thiazolidnones ring at δ (4.52 - 4.71) and (5.70 - 5.81 ) ppm, respectively .13C - NMR spectra of formazans exhibit that the a signal at 156 - 168 ppm (amide carbonyl) , thiazolidinones show a signal at (207.35 - 208 .60) ppm attributed to the C=O ring thiazolidinones.The mass spectra of the formazans compounds [4d ,4e, 4g , 4h] show a molecular ion peak. M+(354 .401 . 516. 498) m/z corresponding to the target compounds. Also, mass spectra of thiazolidinones compounds [5e, 5i] show molecular ion peak. M+ (356 , 369 ) m/z corresponding to the target compounds .This study is also concerned with anti - hyperglycemic activity ,and male mice (Mus musculus Balb/c ) weighing (25 - 35)gm were used for the study of the effects of formazan compound [4e] and thiazolidinone compound [5e] on the blood glucose levels of the animals.Animals are divided into seven different groups, Group (A) : negative control (normal) that is only treated with distilled water (D.W). Group (B) : positive control that is treated with alloxan (125mg/kg) B.W. only to induce diabetes. Group (C) : that is only treated with (DMSO) only. Group (D) : alloxan - induced diabetes mice that are treated with (75 mg/kg) of formazan derivative [4e]. Group (E) : alloxan - induced diabetes mice that are treated with (150 mg/kg) of formazan derivative [4e]. Group (F) : injected alloxan and thiazolidinone [5e] (75 mg/kg). Group (G) : injected alloxan and compound thiazolidinone [5e] (150 mg/kg) .The mice were treated for two weeks and used Colorimetric to Determination of serum Glucose Level by spectrophotometer. The results how that the determination of serum glucose concentration is in males mice groups (A , B , C , D, E , F and G ).A significant decrease can be observed among ( D, E, F and G) groups as compared with group (A) after treatment (2 week) with (75 mg /kg) and (150 mg /kg ) respectively of formazans [4e] and also treatment with(75 mg /kg) and (150 mg /kg ) from thiazolidinone [5e] . while groups (A , C ) do

تحضير وتشخيص قواعد شف ومعقداتها المشتقة من الازاتين واستخدامها في استخلاص ايون النيكل الثنائي == Synthesis and characterization of Schiff Bases and its complexes derived from isatin and using in extraction of nickel ion(II)

Author name: الاء محمد علي عبد الامير
Supervisor name: ساهر عبد الرضا علي | ابراهيم عبود فليفل
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: English
University location: Dhi Qar
First pages:
Abstract: The present work include preparation of three ligands (schiff base) derived from condensation reaction isatin and 5 - Bromoisatin and 5 - Methyl isatin with (2 - aminoBenzylamine) ,to give the following ligands : (z) - 3 - (2 - ((z) - 2 - oxoindolin - 3 - ylideneamino)benzylimino)indolin - 2 - one (z)5 - bromo - 3 - (2 - ((z) - 2 - oxoindolin - 3 - ylideneamino)benzylimino)indolin - 2 - one (z)5 - methyl - 3 - (2 - ((z) - 2 - oxoindolin - 3 - ylideneamino)benzylimino)indolin - 2 - one The new complexes were prepared from the reactions of ligands L1,L2,L3 with the transition metal chlorides (NiCl2.6H2O,CoCl2.6H2O, CrCl3.6H2O).The prepared derivatives and Their complexes were studied and characterized by elemental analysis (CHN),Infrared(IR),Spectroscopy, Nuclear Magnetic Resonance Spectroscopy(1H - NMR),Mass Spectra , Molar conductivity techniques were used. The complexes of [Ni(II), Co(II), Cr(III)] for all ligands have shown octahedral configuration. Shiff base has been stadied by liquid - liquid extraction to words the metal ion Ni2+ from aqueous phase to organic phase .the study of condition o extraction shows that the optimum pH values for extraction was (pH= 8). the suitable concentration of (L3) was(1×10_2M).so the suitable concentration of Ni2+ ion in aqueous solution wich is giving highest distribution ratio (D) was(80μg/ml) .the optimum shaking time to reach the equilibria was(15 minute). The results show that D and (E%) depend on the structure of organic solvent used.the temperature effct that areduce in the efficiency of extraction with increase of temperature means that the reaction is exothermic .The (L3) use in the extraction of nickel from sample of tobacco . it was found that the efficiency of extraction is (E %= 98.98 ) .

تحضير وتشخيص وتقييم الفعالية البايولوجية لبعض مركبات الفورمازان المشتقة من قواعد شف ومركبات الازو الجديدة ومعقداتها مع الكادميوم الثنائي II == Synthesis , Charactrization and Evaluation Biological Activity of some New Formazan Compounds Derived from Schiff Bases and Azo Compounds and Their Complexes With Cadmium(II)

Author name: محمد عبد الحسن شلال
Supervisor name: حيدر عباس مهدي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
First pages:
Abstract: The letter includes the preparation of twenty new derivatives of Formazan compounds that include Schiff bases associated with AZO compounds.The spectrum of spectroscopy (FT.IR) for all compounds, the NMR spectrum, the NMR spectrum of NMR and the CHIS for all compounds and the identification of some of their physical properties such as grade (TPC), and then to prepare four complexes (two of them for morphine and two forformas) as complexes with cadmium ion, to determine optimal conditions for complex formation and then to measure the molecular conductivity of the complex as well as the electronic measurements Wa For magnetic sensitivity. And then studying of biological activity. For some of these vehicles the research has included two main parts : section One : I attended and identified a group of derivatives (Schiff bases) and then were linked through the interaction of the nuts under certain conditions for the preparation of new Formazan compounds containing (Schiff bases - AZO compounds) on the same compound and then attended four complexes of two Schiff bases and two of the Lycandat Formazan The new vehicles have been identified above Section Two : This part of the work was studied by studying the vital effectiveness of some compounds. Schiff bases and Formazan compounds were selected to determine the effect of the active groups of the compound on inhibiting the biological activity of the microorganisms studied in this thesis

تحضير وتشخيص بعض مشتقات قواعد شف والفورمازانات ومعقداتهما واستخدامهما في استخلاص ايون Cr+6 بطريقة استخلاص نقطة الغيمة == Preparation and Characterization of some Schiff base and formazans derivatives and their Complexes and using them in the Extraction of (Cr+6) Ion By Mothed Cloud - Point Extraction

Author name: بتول مهدي صالح
Supervisor name: ساهر عبد الرضا علي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
First pages:
Abstract: This study includes the preparation of ten ligands and it′s complexs : Ligand L4 (N - (4 - ((2 - (phenylcarbamothioyl)hydrazono)methyl)phenyl) acetamide) was prepared by the condensation of (4 - acetamido benzaldehyde) with (4 - phenylthiosemi carbazide). Ligand L5 (1, 3 - bis (2 - hydroxy - 3 - methoxy - (E) - benzylideneamino) eurea) was prepared by the condensation of (o - vanillin) with (carbohydrazide). Formazan F1 (1 - benzoyl - 3 - (2 - hydroxyphenyl) - 5 - phenylformazan) is prepared from coupling the diazonium salt with (L1) proportions Molar (1 : 1). Formazan F2 (3 - (2 - hydroxyphenyl) - 1 - nicotinyl - 5 - phenyl formazan) was prepared by coupling the diazonium salt with (L2) proportions Molar (1 : 1).Complexes were prepared for (L3), (F1) and (F2) by interaction with the salts of the elements NiCl2.6H2O, CoCl2.6H2O, CdCl2.6H2O, CrCl3.6H2O. The ligands and it′s complexes were characterized by using Elemental Analysis (C.H.N) Infrared Spectroscopy(FT - IR), Nuclear Magnetic Resonance Spectroscopy (1H - NMR) , Mass Spectra and Molar Electrical Conductivity and the results were identical to what is expected scientifically. The spatial shape of the complexes prepared is (octahedral). (ligand L1 and formazan F1) on distribution ratio values and percentage of extraction, where results showed that percentage values and distribution ratio in this way increase with increasing concentration of (L1 and F1) where he found that the best distribution ratio (D) and percentage (% E) to extract ion(Cr+6) when concentration (L1 & F1) is (5 * 10 - 4 M).

تحضير , تشخيص ودراسة بيولوجية لمشتقات جديدة من 4,3,1 - ثايادايازول ومعقداتها مع بعض ايونات العناصر الانتقالية == Preparation , Characterization and biological study of new derivatives of 1,3 , 4 - Thiadiazole and their complexes with some transitional element ions

Author name: نعيم عبد السادة بشير الخفاجي
Supervisor name: ابراهيم عبود فليفل
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
First pages:
Abstract: The present study involves preparation of three new ligands derived from the thiadiazole (2,5 - dihydrazineyl - 1,3,4 - thiadiazol) with 1H - indole - 2,3 - dione (Isatin) by the ratio (1 : 2). the ligands L1 and L2 were synthesized from the reaction between thiadiazole derivative with (Benzophenone) by the ratio (1 : 2). The ligand L3 was prepared from thiadiazole derivative and (3 - aminoacetophenone) by the ratio (1 : 2), the following are the structural formulas of the prepared ligands : Prepared the complexes of the transitional elements ions [Cr+3, Fe+3, Co+2, Ni+2 and Cu+2] with ligands (L1, L2 and L3), where the ligands and their complexes characterization by precision analysis of elements (C.H.N.), Infrared spectrum (FT - IR), proton Nuclear Magnetic Resonance (1H - NMR), Mass spectrometry, measurement magnetic sensitivity and measurement molarconductivity the results were practical exactly matching with the molecular and structural formulas of the proposed compounds. Hyperchem was used to draw ligands and their complexes and to show the distribution of electronic density. The data indicates that the configuration of the complexes {[CrL1Cl3], [FeL1 3] , [CoL1 3]}, {[CrL2 3], [FeL2 3] ,[CoL2Cl3]} {[Cr(L3)2Cl ]Cl, 3)2Cl2] and [Co(L )2Cl2]Cl} are octahedral , while the proposed configuration of the complexes {[NiL Cl2], 1Cl2]}, [NiL2Cl2] [CuL2Cl ]} ,{[NiL Cl2] and [CuL3Cl2 are square planer. A study was conducted testing the biological activity for the prepared ligands and their complexes against two types of bacteria (staphylococcus aureus) and (Escherichia coli) compared to the standard inhibitor (Ciprofloxacin), the obtained results confirmed the biological effectiveness of prepared preparations except for the third ligand higher than standard inhibitor (Cipro) towards the bacteria (Escherichia coli), the following complexes also showed (A5, C5, C4, C3 and C1) biological effectiveness towards the bacteria (Escherichia coli) higher than standard inhibitor (Cipro), while the rest complexes showed less effectiveness than the standard inhibitor (Cipro) ) 4and A 3, A2(A ) except the complexesEscherichia colitowards the bacteria (where don't showed any biological effectiveness. Also the study confirmed that ligands and their complexes did not show any biological activity towards the bacteria (staphylococcus aureus).

تحضير وتشخيص وتقيم الفعالية البيولوجية لبعض مركبات الفورمازان المشتقة من قواعد شف الجديدة ومعقداتها مع بعض العناصر الانتقالية == Synthesis, characterization and biological evaluation of some new Formazan compounds derived from Schiff Bases and their complexes with some transition Metals.

Author name: اعراف محمود داود
Supervisor name: حيدر عباس مهدي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: English
University location: Dhi Qar
First pages:
Abstract: This thesis contains three chapters represents, the first chapter introduction and interested in studying the chemistry of schiff base and derivatives of formazan, their complexes in terms of their characteristics, importance and synthesis.The second chapter is interested in describing the chemicals and procedures used in the synthesis of the required compounds, and the study of physical measurements, synthesis methods of compounds and evaluation as well as the biological activity.In this research, four new derivatives of formazan (L3, L4, L5 - 4d), which synthesized from the reaction of Diazonium salt amine with suitable Schiff base (L1, L2 - 2d). The Schiff base can product of different primary amines with several aromatic aldehyde and synthesized both of the (Schiff bases, formazans) suitable complexes.The third chapter Results and Discussion, identified synthesized formazan derivatives as well as Schiff bases prefix and its complexes by appropriate spectral methods including of infrared spectroscopy (FT - IR) for all compounds, Nuclear Magnetic Resonance spectrum (1H - NMR) for all compounds Microanalysis (CHNS) for the majority of compounds as well as Mass spectra. For all complexes were recording certain physical properties, such as melting point (m.p.). Monitoring progress of the chemical reaction by using thin chromatography layer (TLC). We synthesis eight complexes (three from Schiff bases and five from formazan derivatives) were complexes with ions (Co, Ni, Cd), then measuring the molar conductivity of complexes. Then study the biological effectiveness for some compounds have been chosen complexes Schiff bases, as well as formazan complexes to determine the effect of active groups in these compounds to evaluate the efficiency ofXIthe compounds against different type of bacteria.The research also includes a test of biological effectiveness of the prepared ligands and their metallic complexes, where we study response inhibitory to the three types of bacteria, a gram positive type of bacteria (Staphylococcus aureuse) and gram negative type of the bacteria (Escherichia Coli and salmonella species) and compared with the standard inhibitor (Cipro).The biological effectiveness swohs positive results as it was noted The ligand L1, L2, L3, L4, L5 and Schiff base 4d Showed lower efficiency than the standard inhibitor trend three types of bacteria. The prepared complexes from ligands appeared high effective than the effectiveness of the ligands itself The formazan (L3, L4, L5 dna 2d) appeared high effective than the effectiveness of the prepared Schiff base

دراسة كيمو حيوية مقارنه للاجهاد التاكسدي وانماط الدهون في المرضى كبار السن المصابين بمرض الارتجاف الاذني في محافظة ذي قار العراق == A Biochemical Comparative Study of Oxidative Stress and Lipid Profile in Elderly Patients With Atrial Fibrillation in Thi - Qar Governorate/Iraq

Author name: سارة عاشور ساير
Supervisor name: رائد معلك حنون الصالح | عدنان الطعان الخفاجي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: English
University location: Dhi Qar
First pages:
Abstract: Atrial fibrillation (AF) is the most common cardiac arrhythmia in the general population, and a major cause of morbidity and mortality. Lifetime risk for development of AF has been estimated to 1 in 4 in individuals aged 40 years or more.The present study is designed to determine the levels of oxidative stress by measuring lipid peroxidation product (malondialdehyde MDA), antioxidant state by measuring some antioxidants such as (ceruloplasmin Cp, Transferrin Tf, albumin Alb ,uric acid Ua) ,in addition to lipid profile (cholesterol TC, triglyceride TG, high density lipoprotein cholesterol HDL - C, low density lipoprotein cholesterol LDL - C and very low density lipoprotein cholesterol VLDL - C) in atrial fibrillation patients .The study included (150) subjects; (75) normal subjects (control) and (75) patients with atrial fibrillation. The patients are divided into two groups according to the age : (39) elderly patients [the age range (60 - 80) years] and (36) others patients [the age range (20 - 59) years], also patients are divided in to two groups according to the age with one or more risk factor (Hypertention (HTN), Ischemic Heart Disease(IHD), Heart Hailure (HF)) : elderly which included (18) patients (lone AF) , (21) patients (AF with HTN, IHD, HF) and others which included (17) patients (lone AF), (19) patients (AF with HTN, IHD, HF).The normal subjects (control) also divided into two groups according to the age : elderly [the age range (60 - 80) years] and others [the age range (20 - 59) years] .According to age, the results shown significant increase in the concentration of serum (MDA, Cp, uric acid, TC, TG, VLDL - C, LDL - C ) in elderly and other groups in comparison with their control groups (p≤0.05). It was found significant increase in the concentration of serum MDA in elderly group in comparison with other group, also it was found significant increase in the concentration of serum uric acid in control elderly group in comparison withXIVcontrol other group (p≤0.05). The results also showed non significant differences in the concentration of serum (Cp, uric acid, TC,TG, LDL - C, VLDL - C) between elderly and other groups. It was also found non significant differences in the concentration of serum ( Cp, TC, TG, LDL - C, VLDL - C) between control elderly and control other groups (p≤0.05). While serum Alb , serum Tf and serum HDL - C concentrations show a significant decrease in elderly and other groups in comparison with their control groups (p≤0.05). The results showed significant decrease in the concentration of serum HDL - C in control elderly group in comparison with control other group. Also there were no significant differences in the concentration of serum Alb serum Tf and serum HDL - C between elderly and others groups (p≤0.05).According to the age with one or more risk factor (HTN, IHD, HF) the results show a significant increase in the concentration of serum (MDA, Cp , uric acid, TC, TG, VLDL - C , LDL - C ) in elderly and other groups in comparison with their control groups (p≤0.05). It was found a significant increase in the concentration of serum MDA in the groups AF and AF with HTN, IHD, HF ( in elderly groups) in comparison with groups AF and AF with HTN, IHD, HF (in other groups) respectively (p≤0.05). It was also found a significant increase in the concentration of serum uric acid in control elderly groups in comparison with control other groups , also there were no significant differences in the concentration of serum (CP ,TC , TG ,VLDL - C, LDL - C) between elderly and other groups (p≤0.05). serum Alb ,serum Tf and serum HDL - C show a significant decrease in elderly and other groups in comparison with their control groups, also there was significant decrease in the concentration of serum HDL - C in control elderly groups in comparison with control other groups (p≤0.05). It was also found non significant differences in the concentration of serum Alb and serum Tf between elderly and other groups (p≤0.05).

تحضير وتشخيص ودراسة بايولوجية لمشتقات جديدة من - 3,4,0 اوكسادايزول و3,4,0 - ثايادايازول ومعقداتها مع بعض العناصر الانتقالية واستخدامها في استخلاص الكوبلت الثنائي == Synthesis, Characterization, and Biological activity Study of New 1,3,4 - Oxadiazole and 1,3,4 - Thiadiazole Derivatives and Some of Their Transition Metal Complexes and Using in extraction of cobalt ion (ll)

Author name: ازهار حميد كاطع
Supervisor name: ساهر عبد الرضا علي | ابراهيم عبود فليفل
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
First pages:
Abstract: The thesis include preparation and characterization of some new derivations of 1,3,4 - oxadiazole and 1,3,4 - thiadiazole as ligands which are : - L1 = 2,2' - [(1E,2E) - ethane - 1,2 - diylidenedi(2E)hydrazin - 1 - yl - 2 - ylidene]bis(5 - methyl - 1,3,4 - oxadiazole) L2 = 2 - hydrazinyl - 5 - [(2E) - 2 - {(2Z) - 2 - [2 - (5 - hydrazinyl - 1,3,4 - thiadiazol - 2 - yl)hydrazinylidene]ethylidene}hydrazinyl] - 1,3,4 - thiadiazole L3 = 2,2' - {1,3,4 - thiadiazole - 2,5 - diylbis[(1E)hydrazin - 2 - yl - 1 - ylidene(E)methylylidene]}bis(6 - methoxyphenol) with structural formula L1 L2 L3 The new complexes were prepared from the reactions of ligands L1,L2,L3 with the transition metal salts (CrCl3.6H2O, COCl2.6H2O,NiCl2.6H2O) . The elemental analysis (CHN) , Infrared(IR) Spectroscopy , Nuclear Magnetic Resonance Spectroscopy (1H - NMR) , Mass Spectra , Magnetic Susceptibility and Molar conductivity techniques were used to characterize the structural formula of these ligands and their complexes.1) The complexes of [Cr(III) , Co(III)] for all ligands have shown octahedral configuration. 2) Complexes of [Ni(II)] with all ligands have shown square planar configuration.liquid - liquid extraction using L2 as extracting agent , The best results were obtained from liquid - liquid extraction in which Co(ll) had a 95% extraction rate at pH 9 ,temperature degree at 40 C0 Testing the biological activity for ligands and their complex by using spreed method and measurement inhibition zone by using (DMSO) as solvent and erythromycin as standard bactericidal , using in this study two types from bacteria one gram negative bacterial strains (Escherichia coli ) and other isgram positive bacteria strains staphylococcus aureus

تخليق ودراسات طيفية لبعض معقدات العناصر الانتقالية لقواعد شف المشتقة من مركبات ثنائية الامين == Synthesis, Spectroscopic Studies of Some Transition Metal Complexes of Schiff Bases Derived from Diamine Compounds

Author name: فاطمة فلیح حسن الهلالي
Supervisor name: ساھر عبد الرضا علي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
First pages:

Synthesis And Charactrazation Of Some New ? Lactams

Author name: صاحب عوض كاطع الجياشي
Supervisor name: محمود شاكر مكطوف التميمي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: English
University location: Dhi Qar
First pages:

تحضير وتشخيص ودراسة بايولوجية لقواعد شف جديدة مشتقة من 2 - امينو - 5,3 - ثنائي برومو بنزالديهايد ومعقداتها مع بعض العناصر الانتقالية == Preparation, Identification, and Biological Activity of New Some Schiff Bases Derivative from 2 - amino - 3,5 - dibromobenzyldehyd and Their Complexes With Some Transition Metals

Author name: انغام طارق علي الشامي
Supervisor name: حيدر عباس مهدي | فالح حسن الموسوي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
First pages:

تخليق وتشخيص بعض مركبات ? - لاكتام الجديدة == SYNTHESIS AND CHARACTRIZAITION OF NEW ? - LACTAMS

Author name: زينب يحيى كاظم الموسوي
Supervisor name: محمود شاكر مكطوف التميمي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
First pages:

تحضير وتشخيص بعض قواعد شف الجديدة المشتقة ن 2 - هيدروكسي - 1نفثالديهايد ومعقداتها مع بعض العناصر الانتقالية ودراسة فعاليتها كمضادات الاكسدة == Preparation, Identification of Some New Schiff Bases Derivative from 2 - Hydroxy - 1 - naphthaldehyde and Their Complexes With Some Transition Metals and study Anti Oxidant Activities

Author name: رباب لفتة زغير
Supervisor name: حيدر عباس مهدي | علي حسين الموالي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Dhi Qar
First pages:

تحضير ودراسة الفعالية الخافضة للسكر في الدم لبعض مركبات البيتا لاكتام الاحادية والثنائية == Synthesis And Study Hypoglycemic Activity Of Some Mono/Di ? - Lactams Derivatives

Author name: اياد شلاكة فضالة التميمي
Supervisor name: محمود شاكر مكطوف التميمي | محمد عجة عودة
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: English
University location: Dhi Qar
First pages:

تحضير وتشخيص بعض مركبات البيتالاكتام المشتقه من حامض 5 - فنيل فلريك == Synthesis And Charectrazation Of Some ? - Lcatams Dervatives From 5 - Phenyl Valeric Acid A Thesis Submitted To The College Of Science

Author name: تحسين صدام فندي المذخوري
Supervisor name: محمود شاكر مكطوف التميمي | كريم سالم عباس
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: English
University location: Dhi Qar
First pages:

تثبيط تاكل بعض المعادن باستخدام مستخلصات مختلفة لنبات الحنظل == Corrosion Inhibition Of Some Metals Using Different Extracts Of Citrullus Colocynthis

Author name: رشا ناصر عنيد الجابري
Supervisor name: محسن عريبي حسين الدخيلي | حسام محمد كريدي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: English
University location: Dhi Qar
First pages:
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