Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/352639
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dc.date.accessioned2021-12-23T10:25:05Z-
dc.date.available2021-12-23T10:25:05Z-
dc.identifier.urihttp://hdl.handle.net/10603/352639-
dc.description.abstractSchiff bases are used as common ligand in coordination chemistry and newlineit is widely used in medicinal chemistry. The benzoin condensation is a newlinecoupling reaction between two aldehydes that allows the preparation of newlineBenzoin(and#945;-hydroxyketones). Benzoin derivatives of Schiff bases and their newlinetransition metal complexes have been used as medicines and various newlineindustries for very long time. In the research, Schiff base ligands are being newlineprepared by benzoin with various amines such as 1, 4-diaminobutane, newline2,3-diaminopyridine, 1,3-diamino-2-propanol, thiourea, newline2-aminobenzenethiol and 2-aminophenol. Metal complexes have been newlinesynthesized by using the above Schiff base ligands with coordination of newlinecobalt(II), nickel(II), copper(II) and zinc(II) salts. The structure of all the newlinesynthesized ligands and their metal complexes have been characterized newlinethrough spectral studies such as IR, UV-Vis, 1H NMR, 13C NMR, Mass and newlineESR and other physical methods such as elemental analysis, magnetic newlinemoments, molar conductance and thermo gravimetric (TG) analysis. The newlineantimicrobial activity studies are carried out for the Schiff base ligand and newlineits metal complexes. The metal complexes possess a higher antimicrobial newlineactivity than their free ligands. Further the corrosion study also carried out newlineby weight loss method.
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dc.languageEnglish
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dc.rightsuniversity
dc.titleSynthesis Characterization and Biological Studies of some new transition metal complexes of the schiff bases derived from 2 hydroxy 1 2 Di phenyl ethanone
dc.title.alternative
dc.creator.researcherBalamurugan, V
dc.subject.keywordChemistry
dc.subject.keywordChemistry Applied
dc.subject.keywordPhysical Sciences
dc.description.note
dc.contributor.guideShankar, S
dc.publisher.placeTiruchirappalli
dc.publisher.universityBharathidasan University
dc.publisher.institutionDepartment of Chemistry
dc.date.registered
dc.date.completed2015
dc.date.awarded
dc.format.dimensions
dc.format.accompanyingmaterialDVD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Department of Chemistry

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abstract.pdf70.84 kBAdobe PDFView/Open
acknowledgement.pdf91.36 kBAdobe PDFView/Open
certificate.pdf93.18 kBAdobe PDFView/Open
chapter 1.pdf349.79 kBAdobe PDFView/Open
chapter 2.pdf855.41 kBAdobe PDFView/Open
chapter 3.pdf339.6 kBAdobe PDFView/Open
chapter 4.pdf1.27 MBAdobe PDFView/Open
chapter 5.pdf444.79 kBAdobe PDFView/Open
chapter 6.pdf615.62 kBAdobe PDFView/Open
chapter 7.pdf523.66 kBAdobe PDFView/Open
chapter 8.pdf235.14 kBAdobe PDFView/Open
conlusion.pdf175 kBAdobe PDFView/Open
contents.pdf55.4 kBAdobe PDFView/Open
figures.pdf113.57 kBAdobe PDFView/Open
publications.pdf142.04 kBAdobe PDFView/Open
title.pdf102.99 kBAdobe PDFView/Open


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