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dc.contributor.authorSarkar, Madhushree-
dc.date.accessioned2021-11-11T10:42:32Z-
dc.date.available2021-11-11T10:42:32Z-
dc.date.issued2014-
dc.identifier.urihttps://pubs.rsc.org/en/Content/ArticleLanding/2014/RA/c4ra04166f-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3199-
dc.description.abstractThe coordination polymer (CP) of bis(3-pyridyl)butanediamide with Cu(ClO4)2 is a 2D network (CP-3-Cu), which showed two-fold parallel interpenetration, whereas with Cd(ClO4)2 it is a 1D network containing rectangular loops (CP-4-Cd). The metal metathesis of CP-4-Cd with Cu(II) resulted in the isomorphous replacement of the Cd(II) centre with Cu(II). Transmetallation reaction resulted in retaining the structural features of CP-4-Cd even in case of a flexible ligand. The CP formed via transmetallation couldn't be synthesized from a direct reaction of bis(3-pyridyl)butanediamide and Cu(ClO4)2. The transmetallation kinetic studies were performed with an atomic absorption spectrophotometer (AAS) and wavelength dispersive X-ray fluorescence (WDXRF).en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectMetathesisen_US
dc.subjectTransmetallationen_US
dc.titleIs metal metathesis a framework-templating strategy to synthesize coordination polymers (CPs)? Transmetallation studies involving flexible ligandsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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