<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>76(Pt 11)</volume><submitter>Tanaka T</submitter><pubmed_abstract>The title crystalline compound, [Cu&lt;sub>2&lt;/sub>(NCS)&lt;sub>2&lt;/sub>(C&lt;sub>9&lt;/sub>H&lt;sub>16&lt;/sub>N&lt;sub>2&lt;/sub>)&lt;sub>2&lt;/sub>], was obtained from the reaction of copper(I) thio-cyanate (CuSCN) with (&lt;i>N&lt;/i>-prop-2-en-1-yl)piperidine-1-carbo-thio-amide as a chelating and bridging thio-urea ligand in chloro-benzene. The Cu&lt;sub>2&lt;/sub>S&lt;sub>2&lt;/sub> core of the dimeric mol-ecule is situated on a crystallographic inversion centre. The copper atom is coordinated by a thio-cyanate nitro-gen atom, each sulfur atom of the two thio-urea ligands, and the C=C double bond of the ligand in a distorted tetra-hedral geometry. The dimers are linked by N-H⋯S hydrogen bonds, forming a network extending in two dimensions parallel to (100).</pubmed_abstract><journal>Acta crystallographica. Section E, Crystallographic communications</journal><pagination>1712-1715</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7643236</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Crystal structure of bis-[μ-&lt;i>N&lt;/i>-(η&lt;sup>2&lt;/sup>-prop-2-en-1-yl)piperidine-1-carbo-thio-amide-κ&lt;sup>2&lt;/sup> &lt;i>S&lt;/i>:&lt;i>S&lt;/i>]bis-[(thio-cyanato-κ&lt;i>N&lt;/i>)copper(I)].</pubmed_title><pmcid>PMC7643236</pmcid><pubmed_authors>Nakagawa M</pubmed_authors><pubmed_authors>Kashiwagi Y</pubmed_authors><pubmed_authors>Tanaka T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Crystal structure of bis-[μ-&lt;i>N&lt;/i>-(η&lt;sup>2&lt;/sup>-prop-2-en-1-yl)piperidine-1-carbo-thio-amide-κ&lt;sup>2&lt;/sup> &lt;i>S&lt;/i>:&lt;i>S&lt;/i>]bis-[(thio-cyanato-κ&lt;i>N&lt;/i>)copper(I)].</name><description>The title crystalline compound, [Cu&lt;sub>2&lt;/sub>(NCS)&lt;sub>2&lt;/sub>(C&lt;sub>9&lt;/sub>H&lt;sub>16&lt;/sub>N&lt;sub>2&lt;/sub>)&lt;sub>2&lt;/sub>], was obtained from the reaction of copper(I) thio-cyanate (CuSCN) with (&lt;i>N&lt;/i>-prop-2-en-1-yl)piperidine-1-carbo-thio-amide as a chelating and bridging thio-urea ligand in chloro-benzene. The Cu&lt;sub>2&lt;/sub>S&lt;sub>2&lt;/sub> core of the dimeric mol-ecule is situated on a crystallographic inversion centre. The copper atom is coordinated by a thio-cyanate nitro-gen atom, each sulfur atom of the two thio-urea ligands, and the C=C double bond of the ligand in a distorted tetra-hedral geometry. The dimers are linked by N-H⋯S hydrogen bonds, forming a network extending in two dimensions parallel to (100).</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2024-11-06T05:29:39.575Z</modification><creation>2020-11-22T09:39:19Z</creation></dates><accession>S-EPMC7643236</accession><cross_references><pubmed>33209338</pubmed><doi>10.1107/S2056989020013146</doi></cross_references></HashMap>