Please use this identifier to cite or link to this item: http://dspace.cus.ac.in/jspui/handle/1/6361
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dc.contributor.authorSarkar, Prasenjit-
dc.contributor.authorTiwari, Archana-
dc.contributor.authorSarmah, Amrit-
dc.contributor.authorBhandary, Subhrajyoti-
dc.contributor.authorRoy, Ram Kinkar-
dc.contributor.authorMukherjee, Chandan-
dc.date.accessioned2019-09-25T11:42:49Z-
dc.date.available2019-09-25T11:42:49Z-
dc.date.issued2016-
dc.identifier.citationChemical Communications V.52 (70), 2016,10613-10616 pp.en_US
dc.identifier.issn1359-7345-
dc.identifier.urihttps://doi.org/10.1039/c6cc02751b-
dc.identifier.urihttp://dspace.cus.ac.in/jspui/handle/1/6361-
dc.description.abstractRedox-active ligand H4Praedt(AP/AP) experienced C–S bond cleavage during complexation reaction with Co(OAc)2·2H2O in the presence of Et3N in CH3OH in air. Thus, formed complex 1 was composed of two iminobenzosemiquinone radicals in its coordination sphere and an unprecedented stable tethered-vinyl radical. The complex has been characterized by mass, X-ray single crystal, X-band EPR, variable-temperature magnetic moment measurements and DFT based computational study.en_US
dc.language.isoenen_US
dc.publisherThe Royal Society of Chemistryen_US
dc.titleAn elusive vinyl radical isolated as an appended unit in a five-coordinate Co(III)–bis(iminobenzosemiquinone) complex formed via ligand-centered C–S bond cleavageen_US
dc.typeArticleen_US
dc.identifier.Volume52-
dc.identifier.Issue70-
dc.identifier.eissn1364-548X-
Appears in Collections:Archana Tiwari

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