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dc.contributorWichita State University. Department of Chemistryen_US
dc.contributor.authorPanja, Anangamohanen_US
dc.contributor.authorCampana, Charlesen_US
dc.contributor.authorLeavitt, Christopher M.en_US
dc.contributor.authorVan Stipdonk, Michael J.en_US
dc.contributor.authorEichhorn, David M.en_US
dc.date.accessioned2012-02-06T17:17:14Z
dc.date.available2012-02-06T17:17:14Z
dc.date.issued2009-03-02en_US
dc.identifier20161238en_US
dc.identifier9875013en_US
dc.identifierP20 RR017708-030013/ P20 RR017708-040013en_US
dc.identifier.citationInorganica chimica acta. 2009Mar2; 362(4): 1348-1354.en_US
dc.identifier.issn0020-1693en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.ica.2008.06.031en_US
dc.identifier.urihttp://hdl.handle.net/10057/4402
dc.descriptionClick on the DOI link below to access the article.en_US
dc.description.abstractThe syntheses, characterization, and single-crystal X-ray crystal structures are reported for four complexes of iron and cobalt with the pentadentate ligands, 2,6-diacetylpyridinebis(thiosemicarbazone) (H(2)L(1)) and 2,6-diacetylpyridinebis-(phenylthiosemicarbazone) (H(2)L(2)), including a cobalt dimer displaying a deviation from planarity which is unprecedented for this class of ligands and allows the ligand to occupy five positions of a pseudo-octahedral coordination sphere. This dimer reacts with KCN to produce a mononuclear complex of relevance to the active site of cobalt nitrile hydratase.en_US
dc.description.sponsorshipNCRR NIH HHS/ NCRR NIH HHSen_US
dc.format.extent1348-1354en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesInorganica chimica actaen_US
dc.relation.ispartofseriesInorganica Chim Actaen_US
dc.sourceNLMen_US
dc.titleIron and cobalt complexes of 2,6-Diacetylpyridine-bis(R-thiosemicarbazone) (R=H, phenyl) showing unprecedented ligand deviation from planarityen_US
dc.typeArticleen_US
dc.description.versionpeer revieweden_US
dc.rights.holderCopyright © 2009, Elsevieren_US


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