Microsoft Word - 72-85 72 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 Synthesis and Characterization of Some New Complexes With New Schiff Base Type (N2O2) Derived From Glyoxylic Acid and Ethylenediamine. Rehab K. Al-Shemary Jassim S. Sultan Sajid M. Lateef Dept. of Chemistry/College of Education for Pur Sciences (Ibn -Al-Haitham)/ University of Baghdad Received in: 2 /February/2015,Accepted in:7/June/2015 Abstract New tetradentate Schiff base [H2L] namely [2,2׳ -(ethane-1,2- diylbis (azan-1-yl- ylidene) diacetic acid)] was prepared from condensation of ethylenediamine with  glyoxylic acid in ethanol as a solvent in presence of drops of 48% HBr .The structure of ligand (H2L) was characterized by,F-IR, U.V-Vis.,1H-,13C-NMR, pectrophotometer,melting point and elemental microanalysis C.H.N. Metal complexes of the ligand (H2L) in general Molecular formula [M(L)(H2O)2], where M= Co(II), Ni(II), Cu(II), Mn(II) and Hg(II); L=(C6H8N2O4) were synthesized were characterized by, Atomic absorption, F-IR, U.V-Vis. spectra, molar conductivity and magnetic susceptibility.It was found that all the complexes showed octahedral geometries.And in vitro tests for antibacterial activity showed that most of the prepared compounds display a good activity to (Staphylococcus aureus),(Bacillus cereus ) ,(Escherichia coli) and (Pseudomonas). Keywords: Tetradentate Schiff base, Glyoxylic acid, Enylenediamine and Biological activity. 73 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 Introduction Compounds containing an azomethine group (-CH=N-) are known as Schiff-bases. The schiff bases are derived from the condensation reaction of aromatic/aliphatic aldehydes/ketones and aromatic/aliphatic primary amines[1]. The Schiff bases can be used in photochemical, catalytic, biological and electrochemical applications[2]. These are generally bi, tri, tetra-dentate ligands capable of forming very stable complexes with transition metals. The easy preparation and variable geometries of the metal complexes obtained makes them important stereochemical models in transition metal coordination chemistry[3]. Tetradentate Schiff bases type N2O2 are chelating ligands containing O and N donor atoms .It is well known that several Schiff base complexes have anti-inflammatory, antipyretic, analgesic, anti- diabetic, anti-bacterial, anti-cancer and anti-HIV activity [4-7].And they have attracted many authors[8] because of variety of ways to coordinate them with metal ions. Glyoxilic acid and its derivatives play an important role in natural processes, participating in glyoxylate cycle which functions in plants and advancement of inorganic biochemistry[9] . The presnce of aldehyde group in glyoxylic acid allows numerous acyclic derivatives containing (C=N) bond- azomethine and hydrazones [10]. In this paper we rported synthesis of new Schiff base by condinsation glyoxlic acid with ethylenediamine, and it's complexes with Mn(II), Co(II), Ni(II), Cu(II) and Hg(II) were prepared. Also  the antimicrobial and antifungal studies of the Schiff base and the complexes were done by disc diffusion method. Experimental Glyoxylic acid and ethylenadiamine were purchased from sigma chemical Co.(USA). Hydrobromic acid (HBr) (48%) reagent and all other solvents were of high purity (asigma) and were used without further purification).The metal salts used for complexation:Copper(II) chloride dihydrate; Cobalt(II) chloride hexahydrate; Nickel(II) chloride hexahydrate ; Manganese (II) chloride tetrahydrate and Mercury (II) chloride were obtained from British Drug House (BDH) chemical limited company. Instrumentation Melting point was determined on "Gallen kamp Melting point Apparatus".Elemental microanalys C.H.N. were carried out using Euro Vector EA 3000 A Elemental Analysis (Italy).FT-IR measurements were recorded on Shimadzu- 8300 Spectrophotometer in the range of (4000-400cm-1) as KBr disc. Electronic spectra were recorded using U.V-Vis. spectrophotometer type CECIL, England, with quartz cell of (1cm) path length in range (200- 1000)nm in H2O at room temperature.1H and13C-NMR spectra were recorded by using a Bruker 300 MHZ (Switzerland),Chemical shift was recordedin δ(ppm) unit downfield internal reference (TMS),using DMSO as a solvent.Conductictivity measurements were obtained from WTW conductivity meter by using distilled water as a solvent of 10-3M concentration at room temperuture. Magnetic susceptibility measurements were obtained at room temperuture on the solid state applying Faraday's Method using Bruker BM6 instrument. Metal analysis of comlexes were determined by Atomic Absorption(A.A.) technique. Using a shimadzu PR- 5.ORAPHIC PRINTER atomic absorption spectrophotometer. 74 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 Synthesis of [2,2۔ -(ethane -1,2- diylbis (azan-1-yl-ylidene )diacetic acid) (H2L) To a solution of ethylenediamine (0.06g. 1mmole) in (5mL) of ethanol, a solution of glyoxylic acid (0.148g. 2 mmole) in (5 mL) of ethanol with presence of drops of 48% HBr, was added. The mixture was refluxed at 80oC for 3 hrs. upon cooling a dark brown precipitate formed,was filtered off and recrystallized from a hot mixture of [(5mL) methanol, (5mL) acetone and (2mL) distilled water].A pale brown precipitate, yield 90%, melting point 171°C, and elemental microanalysis C.H.N were listed in Table(1). Synthesis of [Cu(L)(H2O)2] complex To a solution of ligand (H2L) (0.172g. 1mmole) in (5 mL) of ethanol, a solution of CuCl2.2H2O (0.170g. 1mmole) in (5 mL) of ethanol ,was added. The precipitate immediately formed, stirring at 50°C for (30 min.), filtered off, recrestallized from a hot of (10mL) methanol, a dark brown precipitate was formed , yield 88%, decomposed at 110 °C .Some physical properties of complex was listed in Table (1). Synthesis of [Mn(L)(H2O)2], [Co(L)(H2O)2], [Ni(L)(H2O)2] and [Hg(L)(H2O)2] complexes A similar method to that mentioned in preparing of [Cu(L)(H2O)2] complex was used to prepare the complexes: [Mn(L)(H2O)2], [Co(L)(H2O)2], [Ni(L)(H2O)2] and[Hg(L)(H2O)2] complexes. Table (1) shows some physical properties of all prepared complexes and their reactants quantities. Results and Discussion The Schiff base (H2L) was synthesized in one step. The structure of (H2L) was checked and confirmed by elemental miocranalyses data which are in good agreement with proposed formula C6H8N2O4. IR Spectrum of the ligand (H2L) The IR spectrum of the (H2L)Fig.(1) shows disappearance of two bands of υNH2 at (3500,3400) cm–1 which due to υasy.NH2 and υsy.NH2 and of appearance new strong bands at (1734, 1647) cm1 are due to υ(HC=N imine)[8-9] compared with precursors . The new two bands at (1436, 1319)cm1 are attributed to υasym.(COO-) and υsym. (COO-) respectively[14-15].The stretching band of middle intensity at (3446) cm-1 attributed to υ (OH) of carboxylic group, which indicates the ligand (H2L) has been obtained. Electronic Spectrum of the ligand (H2L) The U.V-Vis spectrum of ligand (H2L) Fig.(3) displayed two absorption peaks,the first peak at (222)nm (45045)cm-1 was assigned to π–π* electronic transition. The second peak at (356)nm (28089)cm-1 were attributed to n–π* electronic transition.The U.V-Vis spectral data of the ligand (H2L) were given in Table(5) . NMR spectrum for the ligand (H2L) 1H- NMR spectrum of the ligand (H2L) in DMSO–d6 Table(2), Fig. (5) is characterized by the appearance of chemical shift related to the proton of the protons aliphatic (-CH2-CH2-) at (2.50) ppm. The characteristic signals at (8.32-8.51)ppm. are assigned to HC=N. The COOH signal is found at (11.62 )ppm. .The DMSO signal appeared at (2.77-3.87) ppm. [13] . 75 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 13C–NMR of the free ligand(H2L) Table (3)Fig (6) shows the HC=N peak at (43.50) ppm., the COOH peak at (162.44 )ppm, and carbon peaks for aliphatic are detected at (15.20- 18.50) ppm.The peak at (40.25) ppm. assigned to DMSO [7-8]. The IR Spectra for the Complexes The IR spectra provide valuable information regarding the nature of the functional group attached to the metal ion. The IR data are presented in the Table(4). The (IR) spectra of the complexes showed band at the range (1589-1643) cm-1 were assigned to azomethine υ(C=N) groups., which shifted to a lower frequency in comparison with that of the free ligand, indicating the involvement of –C=N nitrogen in coordination to the metal ion[18,19]. Accordingly, the ligand acts as a tetradentate chelating agent, bonded to the metal ion via the nitrogen (–C=N) atoms and the oxygen atoms of carboxylic groups of the Schiff base.The υasym. (COO-) and υsym. (COO-) stretching vibrations of the carboxylate O are observed at (1436,1319) cm-1 for the free ligand (L), these stretching vibrations are shifted to lower or higher frequencies at (1450-1471) cm-1 and (1327-1392) cm-1 for all the complexes, (Δ υasym.- Δ υsym.)=(79-123) cm-1, supporting the idea that the ligand coordinate through deprotonated oxygen of carboxylate [14-15]. The broad bands at range (3402-3444)cm-1 and the weak bands at (925- 968 cm-1) were due to ν(OH) and δ(OH) for all the complexes refer to presence to coordinate aqua (H2O)[20-22]. The new bands at range (594-570) cm-1 were assigned to υ(M-N) mode[18] .The other new bands at (482-465)cm–1 were assigned to (M-O) mode[18] ].Therefore from IR spectra, it is concluded that the ligand behave as anion tetradentate and bind to the metal ions via the two imine N and two carboxylate-O. As shown in fig(2), the Table(4) The (IR) spectra of the [Ni(L)(H2O)2] complex υ(C=N) (1629-1618), υasym. (COO-) (1450), υsym. (COO-) (1327), ν(OH) (3429) ,δ(OH) (968), υ(M- N)(594) and (M-O)(468) The Electronic Absorption Spectral and Magnetic Studies The U.V-Vis spectrum of the Co(II) complex Table(5),Fig(4) displayed four absorption peaks. The first peak at (212)nm (47169 cm–1) was assigned to ligand field, while the second peak at(350) nm (28571) cm–1 refers to charge transfer electronic transition.The third peak at (793)nm (12610) cm–1 and the fourth peak at (817)nm (12240) cm–1 was attibuted to (d-d) electronic trasition type 4T1g(F) →4A2g(F) and 4T1g(F) →4T2g(F) respectively, suggesting high spin octahedral geometry around Co(II) central ion [20]. The magnetic susceptibility measurement for the solid Co(II) complex is (5.42) B.M. also is indicative of four unpaired electron per Co(II) ion suggesting consistency with its octahedral environment[21]. The U.V-Vis spectrum of the Cu(II) complex exhibited three absorption peaks .The first peak at (215) nm (46511 cm–1)   was assigned to ligand field, while the second peak at(357) nm (28011 cm–1)  referred  to  charge transfer electronic transition. The third peak at (741)nm (13495 cm–1) was attributed to (d-d) electronic transtion type 2B1g→2B2g, that is a good suggestment with high spin octahedral geometry [24].The magnetic susceptibility measurement of Cu(II) complex is (1.81) B.M., which suggests the presence of one unpaired electron with its octahedral environment[25]. The U.V-Vis spectrum of the Ni(II) complex displayed four absorption peaks .The first peak at (222)nm (45045cm–1) was refer to ligand field ,  while the second peak at (356)nm (28089cm–1) referred to charge transfer electronic transition.  The third peak at (625)nm (16000cm–1) and  the fourth peak at (892) nm (11210cm–1), were attributed to (d-d) electronic transtion type 3A2g(F) →3T1g(F), 3A2g(F) →3T2g(F), respectively, that is agood 76 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 suggestment with high spin octahedral geometry [22] Fig(4). The magnetic susceptibility measurement for the solid Ni(II) complex is (2.95) B.M. also is indicative of two unpaired electron per Ni (II) ion suggesting consistency with its octahedral geometry[23]. The U.V-Vis spectrum of the Mn(II) complex exhibits four absorption peaks. The first peak at (210) nm (47619 cm–1) was due to ligand field, while the second peak at (354) nm (28248 cm–1) was refer to charge electronic transtion. The third peak at (400)nm (25000cm–1) and the fourth peak at (744) nm (13440 cm–1 ) were assigned to (d-d) forbbiden electronic transtion type 6A1g(F) →4T2g(G) and 6A1g →4T1g(G) respectively,which suggested a high spin octahedral geometry around Mn(II) centeral ion [20]. The magnetic susceptibility measurement of Mn(II) complex is (5.72) B.M.,which suggests the presence of one unpaired electron with its octahedral environment[26]. The U.V-Vis spectrum of the Hg complex displayed two absorption peaks. The first  peak at(212) nm (47619 cm–1)  was assigned to    ligand field , while  the second peak (350) nm referred (28571 cm–1)  was refer to charge electronic transtion only [27,28]. The U.V- Vis spectrum of the Hg(II) complex showed no d-d transitions in the visible region, indicating for  Hg(II), this means electronic transitions happened octahedral geometry has been assigned to the Hg(II) complex. Table(2) and Table-3.According to the elemental analysis Table(1) and FT-IR spectra, the structures of these complexes can be suggested octahedral[29]. Molar Conductivity The molar conductance values of the the complexes in H2O lie in the range 107 to 35 S.cm2mol-1 which is quite lower than that expected for an electrolyte and reveal their non- electrolytic nature as in Table(6) . Biological Activities The biological activities of the prepared ligand and its complexes were studied by using inhibition method [24,25] for four types of pathogenic bacteria. Two types of bacteria were gram positive which are Staphylococcus aureus and Bacillus, the second two were gram negative which are Escherichia coli and Pseudomonas. The data reveal that all compounds have good biological activity and some complexes have higher activities than the free ligand. This may be due to that the chelation considerably reduces the polarity of the metal ion mainly because of partial sharing of its positive charge with the donor groups and possible electron delocalization over the whole chelate ring such, chelation could also enhance the lipophilic character of the central metal atom, which subsequently favors its permeation through the lipid layer of the cell membrane [26,32] . Diameter of zone of inhibition Table (7) and (Figures.8,9,10,11) Conclusion The new schiff ligand (H2L) and metal complexes were aprepared [Mn(L)(H2O)2], [Co(L)(H2O)2], [Ni(L)(H2O)2],  [Cu(L)(H2O)2] and [Hg(L) (H2O)2].The metal (II) ions are coordinated by two carboxylate- O atoms and two imine(H-C=N) atoms.Spectroscopic, structurical and magnetic data show that all complexes are six- coordinate metal complexes owing to the lgation of tetradentate schiff base moieties with two coordinated water as fellows in Scheme(1): 77 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 Scheme (1) References 1. Dominik, C. and Branko, K. (2011) Schiff base derived from 2-hydroxyl-1- naphthaldehyde and liquid- assisted mechanochemical synthesis of its isostructural Cu(II) and Co(II) Complexes, crysteng-comm, 13, 4351-4357. 2. 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Al-Sha'alan,N.H.; (2007) Antimicrobial activity, Spectral, Magnetic and Thermal studies of some transition metal complexes of aSchiff base hydrazone containing aquinoline miety.Molecules.,12: 1080–1091. 80 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 L) and it's complexes2(1): Some physical properties of prepared lignad (H Table and weight of metal salts Solubility Found)Calc% (. Weight (g) 1mmole Metal salt Colour M.P ºC Yi el d % Empirical Formula Metal N H C Water ,DMSO DMF - (15.88) 16.27 (4.65) 3.94 (41.12) 41.86 - pale brown 173 90 L2H = (22.09) 21.80 - - - 0.238 O2.6H2CoCl dark brown <256 89 ]2O)2(H2[Co(L) = (23.38) 22.91 - - - 0.170 O2.2H2CuCl dark brown 110 88 ]2O)2(H2[Cu(L) = (22.09) 21.80 - - - 0.238 O2.6H2NiCl greenth brown 204 94 ]2O)2(H2[Ni(L) = (15.88) 16.27 - - - O2.4H2MnCl white <256 88 ]2O)2(H2[Mn(L) = (15.54) 16.12 - - - 2HgCl brown 123 91 ]2O)2(H2[Hg(L) Table (2): 1H-NMR Chemical Shifts for ligand (H2L) (ppm in DMSO) DMSO Aliphatic protons HC=N COOH 2.5 ppm 2.77-3.87ppm. 8.42ppm 11.62ppm Table (3):13C-NMR Chemical shifts for ligand (H2L) (ppm in DMSO) DMSO Aliphatic crobons HC=N COOH 40.25ppm 15.20-18.50 ppm 143.50ppm 162.44ppm Table (4): Infrared spectral data (wave number υʹ) cm–1for the ligand (H2L), precursors and its complexes Compound υ(OH) υ(C=O) υ(NH2) υ(HC=N)imine υassm.COO – υsymm.COO– ∆υ cm–1 δ(OH)rokin g M–N M–O Glyoxylic acid 3361 1745 - - - - - - - Ethylene diamine - - 3387 3363 - - - - - - H2L 3446 - - 1647 1616 1436 1319 117 - - [CO(L)(H2O)2] 3419 - - 1635 1618 1456 1338 118 966 570 478 [Cu(L)(H2O)2] 3407 - - 1623 1597 1455 1339 116 928 574 468 [Ni(L)(H2O)2] 3429 - - 1629 1618 1450 1327 123 968 594 468 [Mn(L)(H2O)2] 3444 - - 1620 1589 1471 1392 79 925 582 482 [Hg(L)(H2O)2] 3402 - - 1643 1624 1454 1341 113 926 577 450 81 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 Table (5): Electronic spectral data of the ligand (H2L) and its metal complexes Compound µeff ᴧm S.Cm 2 molar -1 λnm υ–wave number cm–1 (εmax molar–1 Assignments H2L - - 222 45045 2295 π→π* [Co(L)(H2O)2] 5.42 83 212 47169 1909 L.F 350 28571 264 C.T 793 12610 22 4T1g(F)→4A2g(P) 817 12240 21 4T1g(F)→4T2g(F) [Cu(L)(H2O)2] 1.81 79 215 46511 2031 L.F 357 28011 392 C.T 741 13495 32 4Eg →4T2g [Ni(L)(H2O)2] 3.23 70 222 45045 2281 L.F 356 28089 238 C.T 625 12610 16 3A2g(F)→3T1g(F) 892 12240 4 3A2g(F)→3T2g(F) [Mn(L)(H2O)2] 5.72 92 210 47619 1821 L.F 354 28248 124 C.T 400 25000 106 6A1g(F)→4T2g(G) 744 13440 8 6A1g(F)→4T1g(G) [Hg(L)(H2O)2] - 72 212 47169 1888 L.F 350 28571 242 C.T Table (6) Diameter of zone of inhibition (mm)       Fig. (1): The IR spectrum of the ligand (H2L) ]2O)2[Hg(L) (H ]2O)2[Ni(L)(H ]2O)2[Mn(L)(H ]2O)2[Cu(L)(H ]2O)2[Co(L) (H L2H Comp. 9 10 13 7 8 2 Escherichia. Coli 18 7 17 15 10 6 Staphylococcus aureus 11 13 22 25 12 5 Bacllus 11 20 12 10 23 1 pseudmonas 82 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015   Fig.(2) :The IR spectrum of [Ni(L)(H2O)2]complex Fig.(3): Electronic spectrum of the ligand(H2L)  Fig.(4):Electronic spectrum of [Ni(L)(H2O)2]complex 83 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 Fig.(5): The1H-NMR spectrum of the ligand (H2L) Fig.(6): The 13C-NMR spectrum of the ligand (H2L)  Fig. (7) :Effect of Escherichia .Coli gram negative  84 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 Fig. (8): Effect of Staphylococcus aureus   Fig.(9): Effect of Bacllus gram Fig.(10): Effect of pseudmonas gram 85 | Chemistry 2015) عام 3العدد ( 28مجلة إبن الھيثم للعلوم الصرفة والتطبيقية المجلد Ibn Al-Haitham Jour. for Pure & Appl. Sci. Vol. 28 (3) 2015 2O2(N تحضير وتشخيص بعض المعقدات الجديدة مع قاعدة شف جديدة نوع( مشتقة من حامض الكاليوكسيلك مع إثيلين ثنائي أمين رحاب كاظم الشمري جاسم شھاب سلطان ساجد محمود لطيف /قسم الكيمياء )أبن الھيثم (جامعة بغداد /كلية التربية للعلوم الصرفة 2015/حزيران/7،قبل البحث في:2015/شباط/2استلم البحث في: الخالصة يليدين) ثناثي حامض - يل -1- دايل بس (أزان -1،2- (أيثان -ʹ2،2[تم تحضير قاعدة شف رباعية السن جديدة أسمھا من تكثيف حامض كاليوكسيلك مع إثيلين ثنائي أمين في االيثانول كمذيب بوجود بعض قطرات من حامض ]الخليك فوق البنفسجية ، –بوساطة أطياف (االشعة تحت الحمراء، المرئية L]2[H) شخص تركيب الليكاند%48الھايدروبروميك ( الرنين النووي المغناطيسي) و التحليل الكمي الدقيق للعناصر وقياس درجة االنصھار .كما تم تحضير معقدات لليكاند شخصت L4O2N8H6= M; (C (II)Co ,(II), Mn(II),Cu(II)Hg= ( أذ H)2O)2[M(L) [بالصيغة الجزيئية العامة فوق البنفسجية و االمتصاص –المعقدات المحضرة بوساطة أطياف تحت الحمراء ، طيف االشعة ، طيف االشعة المرئية وقد وجد أن الشكل الھندسي لجميع المعقدات المحضرة ھو ثماني .الذري التوصيلية الموالرية والحساسية المغناطيسية لبعض أنواع من البكتريا ھي جيدة فعالية مضادة ا ذومركبات المحضرة أغلبھوقد وجد أن ال.السطوح :(Escherichiacoli),(Bacillus), (Staphylococcus aureus) و(Pesudomonas). .قاعدة شف رباعية السن ، حامض كاليوكسيلك ،اثيلين ثنائي امين والفعالية البايولوجية : كلمات مفتاحيةال