<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>66(Pt 7)</volume><submitter>Tsai YF</submitter><pubmed_abstract>In the title compound, [N(C(4)H(9))(4)][V(C(23)H(21)NS(3)Si)(2)]·4CH(3)CN, the V(III) atom (site symmetry ) is coordinated by two N,S,S'-tridentate 4,4'-dimethyl-2,2'-(3,7-dimethyl-1H-4,2,1-benzothiaza-siline-1,1-di-yl)dibenzene-thiol-ate ligands in a distorted trans-VN(2)S(4) octa-hedral geometry. The complete cation is generated by crystallographic twofold symmetry, with the V atom lying on the rotation axis. The unusual ligand arose from nucleophilic attack on the coordinated nitrile by the thiol-ate precursor and reduction of nitrile to the imidate.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>m844</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3006863</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tetra-butyl-ammonium bis-[4,4'-dimethyl-2,2'-(3,7-dimethyl-1H-4,2,1-benzothiaza-siline-1,1-di-yl)dibenzene-thiol-ato]vanadium(III) acetonitrile tetra-solvate.</pubmed_title><pmcid>PMC3006863</pmcid><pubmed_authors>Hsu HF</pubmed_authors><pubmed_authors>Hsu KF</pubmed_authors><pubmed_authors>Wang JC</pubmed_authors><pubmed_authors>Tsai YF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tetra-butyl-ammonium bis-[4,4'-dimethyl-2,2'-(3,7-dimethyl-1H-4,2,1-benzothiaza-siline-1,1-di-yl)dibenzene-thiol-ato]vanadium(III) acetonitrile tetra-solvate.</name><description>In the title compound, [N(C(4)H(9))(4)][V(C(23)H(21)NS(3)Si)(2)]·4CH(3)CN, the V(III) atom (site symmetry ) is coordinated by two N,S,S'-tridentate 4,4'-dimethyl-2,2'-(3,7-dimethyl-1H-4,2,1-benzothiaza-siline-1,1-di-yl)dibenzene-thiol-ate ligands in a distorted trans-VN(2)S(4) octa-hedral geometry. The complete cation is generated by crystallographic twofold symmetry, with the V atom lying on the rotation axis. The unusual ligand arose from nucleophilic attack on the coordinated nitrile by the thiol-ate precursor and reduction of nitrile to the imidate.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jun</publication><modification>2025-04-26T05:08:37.162Z</modification><creation>2019-03-27T00:00:34Z</creation></dates><accession>S-EPMC3006863</accession><cross_references><pubmed>21587755</pubmed><doi>10.1107/S1600536810022014</doi></cross_references></HashMap>