Synthesis, Characterization and Biological Activity of Mixed Ligand (Imine of Benzidine and 1,10-Phenanthroline) Complexes with Fe(II), Co(II), Ni(II) and Cu(II) Ions

dc.citation.epage24
dc.citation.issue1
dc.citation.spage15
dc.contributor.affiliationUniversity of Kerbala
dc.contributor.authorHassan, Zainab M.
dc.contributor.authorAlattar, Rawaa A.
dc.contributor.authorAbass, Suhad Kareem
dc.contributor.authorMihsen, Hayder Hamied
dc.contributor.authorAbbas, Zainab Fadhil
dc.coverage.placenameЛьвів
dc.coverage.placenameLviv
dc.date.accessioned2024-01-22T10:41:33Z
dc.date.available2024-01-22T10:41:33Z
dc.date.created2022-03-16
dc.date.issued2022-03-16
dc.description.abstractЗа реакцією первинного ліганду (іміну бензидину) (H2L) та вторинного ліганду (1,10-фенантролін) (L`) з йонами металів Fe(II), Co(II), Ni(II) та Cu(II) у мольному співвідношенні 1:2:2 синтезовані бінуклеарні металічні комплекси. За допомогою елементарного аналізу, FT-IR, UV-VIS, магнітної сприйнятливості, молярної провідності, 1H ЯМР та термогравіметричного аналізу TGA-DTA визначено характеристику комплексів. Показано, що комплекси з Fe(II), Co(II) і Ni(II) мають восьмигранну геометрію, тоді як комплекс з Cu(II) має квадратну площинну геометрію. Всі синтезовані комплекси стійкі і можуть зберігатися місяцями без суттєвих змін. З використанням дифузійних агарових пластинок проведено оцінку антибактеріальної активності одержаних сполук стосовно двох видів бактерій, грампозитивної та грамнегативної (Kelbsiella та Proteus). Встановлено, що бактерія Klebsiella є більш чутливою до цих сполук, ніж Proteus. Показано, що синтезовані сполуки мають більший вплив на бактерії у порівнянні з антибіотиком (Амікацин).
dc.description.abstractIn this paper, binuclear metal complexes of the metal ions Fe(II), Co(II), Ni(II) and Cu(II) were synthesized by the reaction of the primary ligand (imine of benzidine) (H2L) and the secondary ligand (1,10-phenanthroline) (L`) with these metal ions in a molar ratio of 1:2:2, respectively. The complexes were characterized using CHN elemental analysis, FT-IR, UV-Vis, magnetic susceptibility, molar conductivity, 1H NMR, and TGA-DTA thermogravimetric analysis. According to the results obtained from the elemental analysis and spectral measurements where complexes of Fe(II), Co(II) and Ni(II) have octahedral geometry, while the complex with Cu(II) has a square planar geometry. All the prepared complexes are wholly stable and can keep for months without any significant change. The antibacterial activities of the prepared compounds were evaluated with regard to two bacteria species, gram-negative Proteus and Kelbsiella, by using diffusion agar plates. The inhibition zone diameter around the holes indicated the sensitivity of the bacteria to these compounds, where the Klebsiella bacteria were revealed to be more highly sensitive to these compounds than Proteus bacteria. All synthesized complexes showed more significant effects against Kelbsiella and Protea than the antibiotic (Amikacin).
dc.format.extent15-24
dc.format.pages10
dc.identifier.citationSynthesis, Characterization and Biological Activity of Mixed Ligand (Imine of Benzidine and 1,10-Phenanthroline) Complexes with Fe(II), Co(II), Ni(II) and Cu(II) Ions / Zainab M. Hassan, Rawaa A. Alattar, Suhad Kareem Abass, Hayder Hamied Mihsen, Zainab Fadhil Abbas // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2022. — Vol 16. — No 1. — P. 15–24.
dc.identifier.citationenSynthesis, Characterization and Biological Activity of Mixed Ligand (Imine of Benzidine and 1,10-Phenanthroline) Complexes with Fe(II), Co(II), Ni(II) and Cu(II) Ions / Zainab M. Hassan, Rawaa A. Alattar, Suhad Kareem Abass, Hayder Hamied Mihsen, Zainab Fadhil Abbas // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2022. — Vol 16. — No 1. — P. 15–24.
dc.identifier.doidoi.org/10.23939/chcht16.01.015
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/60956
dc.language.isoen
dc.publisherВидавництво Львівської політехніки
dc.publisherLviv Politechnic Publishing House
dc.relation.ispartofChemistry & Chemical Technology, 1 (16), 2022
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dc.relation.referencesen[1] Yousif, E.; Majeed, A.; Al-Sammarrae, K.; Salih N.; Salimon J.; Abdullah B. Metal Complexes of Schiff base: Preparation, Characterization and Antibacterial Activity. Arab. J. Chem. 2017, 10, 1639-1644. https://doi.org/10.1016/j.arabjc.2013.06.006
dc.relation.referencesen[2] Ejidike, I.; Ajibade, P. Ruthenium(III) Complexes of Heterocyclic Tridentate (ONN) Schiff Base: Synthesis, Characterization and its Biological Properties as an Antiradical and Antiproliferative Agent. Int. J. Mol. Sci. 2016, 17, 60. https://doi.org/10.3390/ijms17010060
dc.relation.referencesen[3] Murtaza, S.; Akhtar, M.; Kanwal, F.; Abbas, A.; Ashiq, S.; Shamim S. Synthesis and Biological Evaluation of Schiff Bases of 4-Aminophenazone as an Anti-inflammatory, Analgesic and Antipyretic Agent. J. Saudi Chem. Soc. 2017, 21, 359-372. https://doi.org/10.1016/j.jscs.2014.04.003
dc.relation.referencesen[4] Divya, K.; Pinto, G.; Pinto, A. Application of Metal Complexes of Schiff Bases as an Antimicrobial Drug: A Review of Recent Works. Int. J. Curr. Pharm. Res. 2017, 9, 27-30. https://doi.org/10.22159/ijcpr.2017.v9i3.19966
dc.relation.referencesen[5] Anacona, J.; Mago, K.; Camus, J. Antibacterial Activity of Transition Metal Complexes with a Tridentate NNO Amoxicillin Derived Schiff Base. Synthesis and Characterization. Appl. Organomet. Chem. 2018, 32, 1. https://doi.org/10.1002/aoc.4374
dc.relation.referencesen[6] Barnabas, M.; Parambadath, S.; Nagappan, S.; Ha, C. Sulfamerazine Schiff-Base Complex Intercalated Layered Double Hydroxide: Synthesis, Characterization, and Antimicrobial Activity. Heliyon. 2019, 5, e01521. https://doi.org/10.1016/j.heliyon.2019.e01521
dc.relation.referencesen[7] Sunday Nworie, F. Bis(Salicylidene) Ethylenediamine(salen) and bis(Salicylidene) Ethylenediamine-Metal Complexes: from Structure to Biological Activity. J. Anal. Pharm. Res. 2016, 3, 1. https://doi.org/10.15406/japlr.2016.03.00076
dc.relation.referencesen[8] Akhter, S.; Zaman, H.; Mir, S. Dar, A.M. Synthesis of Schiff Base Metal Complexes: A Concise Review. Eur. Chem. Bull. 2017, 6, 475-483. https://doi.org/10.17628/ecb.2017.6.475-483
dc.relation.referencesen[9] Rao, N.; Mishra, D.; Maurya, R. Synthesis and Characterisation of Some Novel CIS-Dioxo-Molybdenum(VI) Complexes of Schiff Bases Derived from Salicylaldehyde. Synth. React. Inorg. Met. Chem. 1995, 25, 437-449. https://doi.org/10.1080/15533179508218232
dc.relation.referencesen[10] Felthouse, T.; Hendrickson, D. Magnetic Exchange Interactions in Binuclear Transition-Metal Complexes. 17. Benzidine and p-Phenylenediamine, Extended Aromatic Diamine Bridging Ligands in Binuclear Copper(II) 2,2',2''-triaminotriethylamine and Vanadyl Bis(hexafluoroacetylacetonate) Complexes. Inorg. Chem. 1978, 17, 2636-2648. https://doi.org/10.1021/ic50187a054
dc.relation.referencesen[11] El-Tabl, A. Synthesis and Physico-Chemical Studies on Cobalt(II), Nickel(II) and Copper(II) Complexes of Benzidine Diacetyloxime Transit. Met. Chem. 2002, 27, 166-170. https://doi.org/10.1023/A:1013952726823
dc.relation.referencesen[12] Zhao, P.; Zhai, S.; Dong, J., Gao, L.; Liu X.; Wang L.; Kong J.; Li L. Synthesis, Structure, DNA Interaction, and SOD Activity of Three Nickel(II) Complexes Containing L-Phenylalanine Schiff Base and 1,10-Phenanthroline. Bioinorg. Chem. Appl. 2018, 2018, 8478152. https://doi.org/10.1155/2018/8478152
dc.relation.referencesen[13] Patel, R. N.; Singh, N. G.; Gundla, V.L.N. Synthesis, Structure and Properties of Ternary Copper(II) Complexes of ONO Donor Schiff Base, Imidazole, 2,2′-Bipyridine and 1,10-Phenanthroline. Polyhedron 2006, 25, 3312-3318. https://doi.org/10.1016/j.poly.2006.06.017
dc.relation.referencesen[14] Kosolapov, D.; Kuschak, P.; Vainshtein, M.; Vatsourina, A.V.; Weibner, A.; Kästner, M.; Müller, R.A. Microbial Processes of Heavy Metal Removal from Carbon-Deficient Effluents in Constructed Wetlands. Eng. Life Sci. 2004, 4, 403-411. https://doi.org/10.1002/elsc.200420048
dc.relation.referencesen[15] Selvamohan, T.; Sandhya, V. Studies on Bactericidal Activity of Different Soaps Against Bacterial Strains J. Microbiol. Biotechnol. Res. 2012, 2, 646-650.
dc.relation.referencesen[16] Bauer, A.W.; Kirby, W.M.M.; Sherris, J.C.; Turck, M. Antibiotic Susceptibility Testing by a Standardized Single Disk Method: Am. J. Clin. Pathol. 1966, 45, 493-496. https://doi.org/10.1093/ajcp/45.4_ts.493
dc.relation.referencesen[17] More, G.; Raut, D.; Aruna, K.; Bootwala, S. Synthesis, Spectroscopic Characterization and Antimicrobial Activity Evaluation of New Tridentate Schiff Bases and their Co(II) Complexes. J. Saudi Chem. Soc. 2017, 21, 954-964. https://doi.org/10.1016/j.jscs.2017.05.002
dc.relation.referencesen[18] Singh, D.K.; Singh, N.; Singh, R. Transethmoidal Meningocele: an Unusual Complication of Intracranial Neoplasm. Int. J. Inorg. Chem. 2013, 2013, 1. https://doi.org/10.1136/bcr-2013-009200
dc.relation.referencesen[19] Krishnaveni, G.; Mubarak, M.S; Kiruthika, M.; Elayaperumal, R. Synthesis, Spectral Characterization, Electrochemical Behaviour, In vitro Antimicrobial and DPPH Radical Scavenging Activities of Iron (II), Cobalt (II) Complexes with Imidazolyl Terpyridine. Der Chem. Sin. [Online] 2017, 8. https://www.imedpub.com/articles/synthesis-spectral-characterization-ele... (accessed Oct 06, 2021).
dc.relation.referencesen[20] Larsen, C.; Wenger, O. Photoredox Catalysis with Metal Complexes Made from Earth-Abundant Elements. Chem A Eur J., 2018, 24, 2039-2058. https://doi.org/10.1002/chem.201703602
dc.relation.referencesen[21] San Tan, S.; Yanagisawa, S.; Inagaki, K.; Kassim, M.B.; Morikawa, Y. Experimental and Computational Studies on Ruthenium(ii) bis-Diimine Complexes of N,N′-chelate Ligands: the Origin of Changes in Absorption Spectra Upon Oxidation and Reduction. Phys. Chem. Chem. Phys. 2019, 21, 7973. https://doi.org/10.1039/P.8CP05016C
dc.relation.referencesen[22] Goodgame, D.M.L.; Goodgame, M.; Cotton, F.A. Electronic Spectra of Some Tetrahedral Nickel(II) Complexes. J. Am. Chem. Soc., 1961, 83, 4161-4167. https://doi.org/10.1021/ja01481a014
dc.relation.referencesen[23] Lever, A. Inorganic Electronic Spectroscopy, 2nd ed.; Elsevier Pub. Co: Amsterdam, New York, 1968.
dc.relation.referencesen[24] Mihsen, H.H.; Shareef N.D. Synthesis, Characterization of Mixed-Ligand Complexes Containing 2,2-Bipyridine and 3-Aminopropyltriethoxysilane. J. Phys. Conf. Ser. 2018, 1032, 1. https://doi.org/10.1088/1742-6596/1032/1/012066
dc.relation.referencesen[25] Venanzi, L.M. Tetrahedral Complexes of Nickel (II) and the Factors Determining their Formation. J. Inorg. Nucl. Chem. 1958, 8(C), 137-142. https://doi.org/10.1016/0022-1902(58)80175-X
dc.relation.referencesen[26] Knittl, E.T.; Abou-Hussein, A.A.; Linert, W. Syntheses, Characterization, and Biological Activity of Novel Mono- and Binuclear Transition Metal Complexes with a Hydrazone Schiff Base Derived from a Coumarin Derivative and Oxalyldihydrazine. Monatshefte für Chemie-Chemical Mon. 2018, 149, 431-443. https://doi.org/10.1007/s00706-017-2075-9
dc.relation.referencesen[27] Mihsen, H.H.; Abass, S.K.; Abass, A.K.; Hussain, K.A.; Abbas, Z.F. Template Synthesis of Sn(II), Sn(IV) and Co(II) Complexes via 3-Aminopropyltriethoxysilane and Salicylaldehyde and Evaluate their Antibacterial Sensitivity. Asian J. Chem. 2018, 30, 2277-2280. https://doi.org/10.14233/ajchem.2018.21439
dc.relation.referencesen[28] Czakis-Sulikowska, D.; Malinowska, A.; Radwañska-Doczekalska, J. Synthesis, Properties and Thermal Decomposition of Bipyridine-Oxalato Complexes with Mn(II), Co(II), Ni(II) and Cu(II). Pol. J. Chem. 2000, 74, 607-614.
dc.relation.referencesen[29] Pearson, R.G. Hard and Soft Acids and Bases. J. Am. Chem. Soc. 1963, 85, 3533-3539. https://doi.org/10.1021/ja00905a001
dc.relation.referencesen[30] Sundaram, S.; Kanniappan, G.V.; Kannappan, P. Enzymatic and Non Enzymatic Antioxidant Activity of Tabernaemontana divaricate R.Br. against DEN and Fe-NTA Induced Renal Damage in Wistar Albino Rats. J. Appl. Pharm. Sci. 2015, 5, 33-37. https://doi.org/10.7324/JAPS.2015.50506
dc.relation.urihttps://doi.org/10.1016/j.arabjc.2013.06.006
dc.relation.urihttps://doi.org/10.3390/ijms17010060
dc.relation.urihttps://doi.org/10.1016/j.jscs.2014.04.003
dc.relation.urihttps://doi.org/10.22159/ijcpr.2017.v9i3.19966
dc.relation.urihttps://doi.org/10.1002/aoc.4374
dc.relation.urihttps://doi.org/10.1016/j.heliyon.2019.e01521
dc.relation.urihttps://doi.org/10.15406/japlr.2016.03.00076
dc.relation.urihttps://doi.org/10.17628/ecb.2017.6.475-483
dc.relation.urihttps://doi.org/10.1080/15533179508218232
dc.relation.urihttps://doi.org/10.1021/ic50187a054
dc.relation.urihttps://doi.org/10.1023/A:1013952726823
dc.relation.urihttps://doi.org/10.1155/2018/8478152
dc.relation.urihttps://doi.org/10.1016/j.poly.2006.06.017
dc.relation.urihttps://doi.org/10.1002/elsc.200420048
dc.relation.urihttps://doi.org/10.1093/ajcp/45.4_ts.493
dc.relation.urihttps://doi.org/10.1016/j.jscs.2017.05.002
dc.relation.urihttps://doi.org/10.1136/bcr-2013-009200
dc.relation.urihttps://www.imedpub.com/articles/synthesis-spectral-characterization-ele..
dc.relation.urihttps://doi.org/10.1002/chem.201703602
dc.relation.urihttps://doi.org/10.1039/C8CP05016C
dc.relation.urihttps://doi.org/10.1021/ja01481a014
dc.relation.urihttps://doi.org/10.1088/1742-6596/1032/1/012066
dc.relation.urihttps://doi.org/10.1016/0022-1902(58)80175-X
dc.relation.urihttps://doi.org/10.1007/s00706-017-2075-9
dc.relation.urihttps://doi.org/10.14233/ajchem.2018.21439
dc.relation.urihttps://doi.org/10.1021/ja00905a001
dc.relation.urihttps://doi.org/10.7324/JAPS.2015.50506
dc.rights.holder© Національний університет “Львівська політехніка”, 2022
dc.rights.holder© Hassan Z. M., Alattar R. A., Abass S. K., Mihsen H. H., Abbas Z. F., Hussain K. A., 2022
dc.subjectоснова Шиффа
dc.subjectбінуклеарні металічні комплекси
dc.subject1
dc.subject10-фенантролін
dc.subjectтермогравіметричний аналіз
dc.subjectбіологічна активність
dc.subjectSchiff base
dc.subjectbinuclear metal complexes
dc.subject1
dc.subject10-phenanthroline
dc.subjectthermogravimetric analysis
dc.subjectbiological activities
dc.titleSynthesis, Characterization and Biological Activity of Mixed Ligand (Imine of Benzidine and 1,10-Phenanthroline) Complexes with Fe(II), Co(II), Ni(II) and Cu(II) Ions
dc.title.alternativeСинтез, характеристика і біологічна активність суміші лігандів (іміну бензидину та 1,10-фенантроліну) та йонів Fe(II), Co(II), Ni(II) та Cu(II)
dc.typeArticle

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