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dc.contributor.authorAgarwal, Shilpi-
dc.date.accessioned2014-12-03T06:22:50Z-
dc.date.available2014-12-03T06:22:50Z-
dc.date.issued2008-
dc.identifierM.Techen_US
dc.identifier.urihttp://hdl.handle.net/123456789/12819-
dc.guideSingh, U. P.-
dc.description.abstractThe reaction of iron (II) chloride with 3,5-diisopropylpyrazole resulted in the formation of [(3,5-Pr12pzH)2FeC12]. The same reaction mixture in presence of different para substituted benzoate (p-X-OBz) and excess amount of H202 gave mononuclear Fe(III) complex [Fe(3-OCMe2,5-Pr'2pz)3].2X-OBz (where X = H, Cl, F, CH3, OCH3, CHO, CN, NH2, NO2). In these complexes one of the methine groups present in each of three 3,5-diisopropylpyrazole rings were oxidized during • oxidation and coordinated to iron centre. These complexes were characterized by elemental analysis, IR, UV-Visible and thermal studiesen_US
dc.language.isoenen_US
dc.subjectCHEMISTRYen_US
dc.subjectMETAL COMPLEXESen_US
dc.subjectC-H BOND ACTIVATIONen_US
dc.subjectUV-VISIBLEen_US
dc.titleSYNTHESIS AND ANALYTICAL STUDIES ON METAL COMPLEXES FOR C-H BOND ACTIVATIONen_US
dc.typeM.Tech Dessertationen_US
dc.accession.numberG13990en_US
Appears in Collections:MASTERS' THESES (Chemistry)

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