Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/21195
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dc.contributor.authorMaurya, Mannar R-
dc.contributor.authorAgarwal, Neeraj-
dc.contributor.authorKhurana, Shilpa-
dc.date.accessioned2013-09-16T09:10:28Z-
dc.date.available2013-09-16T09:10:28Z-
dc.date.issued2000-10-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21195-
dc.description1093-1097en_US
dc.description.abstractThe flexibly-bridged tetraanionic hexadentate ligands (LH4), methylenbis(salicylaldehyde-o-hydroxybenzylamine) [CH2(H2sal-OHYBA)2] and methylenebis(salicylaldehyde –o-aminobenzylalcohol) [CH2(H2sal-OABA)2] react with acetates of copper(II), nickel(II), cobalt(II), dioxouranium(VI) to give the corresponding metal complexes of formula [Cu2L], [Ni2L.4H2O), [Co2L.4H2O] and [(UO2)2L.2CH3OH], respectively. Reaction of these ligands with [MO2(acac)2](M=Mo, W) in refluxing methanol affords [(MO2)2L.nCH3OH] (n=0 or 2). Thermogravimetric analyses confirm the coordination of H2O/CH3OH in complexes.1H NMR spectral data of molybdenum, tungsten and uranium complexes suggest coordination of the ligands through deprotonated phenolic/enolic oxygen and azomethine nitrogen atoms. Electronic spectral data suggest square planar structure for copper complexes while an octahedral structure for other complexes.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.39A(10) [October 2000]en_US
dc.titleSynthesis and characterization of metal complexes of methylene bridged hexadentate tetraanionic ligandsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.39A(10) [October 2000]

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