<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>78(Pt 3)</volume><submitter>Nather C</submitter><pubmed_abstract>Reaction of Co(ClO&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>·6H&lt;sub>2&lt;/sub>O with cyclam (cyclam = 1,4,8,11-tetra-aza-cyclo-tetra-deca-ne) and Na&lt;sub>3&lt;/sub>SbS&lt;sub>4&lt;/sub>·9H&lt;sub>2&lt;/sub>O (Schlippesches salt) in a mixture of aceto-nitrile and water leads to the formation of crystals of the title compound with the composition {[Co&lt;sub>3&lt;/sub>(SbS&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>(C&lt;sub>10&lt;/sub>H&lt;sub>24&lt;/sub>N&lt;sub>4&lt;/sub>)&lt;sub>3&lt;/sub>]·2CH&lt;sub>3&lt;/sub>CN·2H&lt;sub>2&lt;/sub>O} &lt;sub>&lt;i>n&lt;/i>&lt;/sub> or {[(Co-cyclam)&lt;sub>3&lt;/sub>(SbS&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>]·2(aceto-nitrile)·2H&lt;sub>2&lt;/sub>O} &lt;sub>&lt;i>n&lt;/i>&lt;/sub> . The crystal structure of the title compound consists of three crystallographically independent [Co-cyclam]&lt;sup>2+&lt;/sup> cations, which are located on centers of inversion, one [SbS&lt;sub>4&lt;/sub>]&lt;sup>3-&lt;/sup> anion, one water and one aceto-nitrile mol-ecule that occupy general positions. The aceto-nitrile mol-ecule is disordered over two orientations and was refined using a split model. The Co&lt;sup>II&lt;/sup> cations are coordinated by four N atoms of the cyclam ligand and two &lt;i>trans&lt;/i>-S atoms of the tetra-thio-anti-monate anion within slightly distorted octa-hedra. The unique [SbS&lt;sub>4&lt;/sub>]&lt;sup>3-&lt;/sup> anion is coordinated to all three crystallographically independent Co&lt;sup>II&lt;/sup> cations and this unit, with its symmetry-related counterparts, forms rings composed of six Co-cyclam cations and six tetra-thio-anti-monate anions that are further condensed into layers. These layers are perfectly stacked onto each other so that channels are formed in which acetontrile solvate mol-ecules that are hydrogen bonded to the anions are embedded. The water solvate mol-ecules are located between the layers and are connected to the cyclam ligands and the [SbS&lt;sub>4&lt;/sub>]&lt;sup>3-&lt;/sup> anions &lt;i>via&lt;/i> inter-molecular N-H⋯O and O-H⋯S hydrogen bonding.</pubmed_abstract><journal>Acta crystallographica. Section E, Crystallographic communications</journal><pagination>270-274</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8900515</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis and crystal structure of poly[[di-μ&lt;sub>3&lt;/sub>-tetra-thio-anti-monato-tris-[(cyclam)cobalt(II)]] aceto-nitrile disolvate dihydrate] (cyclam = 1,4,8,11-tetra-aza-cyclo-tetra-deca-ne).</pubmed_title><pmcid>PMC8900515</pmcid><pubmed_authors>Nather C</pubmed_authors><pubmed_authors>Danker F</pubmed_authors><pubmed_authors>Bensch W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and crystal structure of poly[[di-μ&lt;sub>3&lt;/sub>-tetra-thio-anti-monato-tris-[(cyclam)cobalt(II)]] aceto-nitrile disolvate dihydrate] (cyclam = 1,4,8,11-tetra-aza-cyclo-tetra-deca-ne).</name><description>Reaction of Co(ClO&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>·6H&lt;sub>2&lt;/sub>O with cyclam (cyclam = 1,4,8,11-tetra-aza-cyclo-tetra-deca-ne) and Na&lt;sub>3&lt;/sub>SbS&lt;sub>4&lt;/sub>·9H&lt;sub>2&lt;/sub>O (Schlippesches salt) in a mixture of aceto-nitrile and water leads to the formation of crystals of the title compound with the composition {[Co&lt;sub>3&lt;/sub>(SbS&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>(C&lt;sub>10&lt;/sub>H&lt;sub>24&lt;/sub>N&lt;sub>4&lt;/sub>)&lt;sub>3&lt;/sub>]·2CH&lt;sub>3&lt;/sub>CN·2H&lt;sub>2&lt;/sub>O} &lt;sub>&lt;i>n&lt;/i>&lt;/sub> or {[(Co-cyclam)&lt;sub>3&lt;/sub>(SbS&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>]·2(aceto-nitrile)·2H&lt;sub>2&lt;/sub>O} &lt;sub>&lt;i>n&lt;/i>&lt;/sub> . The crystal structure of the title compound consists of three crystallographically independent [Co-cyclam]&lt;sup>2+&lt;/sup> cations, which are located on centers of inversion, one [SbS&lt;sub>4&lt;/sub>]&lt;sup>3-&lt;/sup> anion, one water and one aceto-nitrile mol-ecule that occupy general positions. The aceto-nitrile mol-ecule is disordered over two orientations and was refined using a split model. The Co&lt;sup>II&lt;/sup> cations are coordinated by four N atoms of the cyclam ligand and two &lt;i>trans&lt;/i>-S atoms of the tetra-thio-anti-monate anion within slightly distorted octa-hedra. The unique [SbS&lt;sub>4&lt;/sub>]&lt;sup>3-&lt;/sup> anion is coordinated to all three crystallographically independent Co&lt;sup>II&lt;/sup> cations and this unit, with its symmetry-related counterparts, forms rings composed of six Co-cyclam cations and six tetra-thio-anti-monate anions that are further condensed into layers. These layers are perfectly stacked onto each other so that channels are formed in which acetontrile solvate mol-ecules that are hydrogen bonded to the anions are embedded. The water solvate mol-ecules are located between the layers and are connected to the cyclam ligands and the [SbS&lt;sub>4&lt;/sub>]&lt;sup>3-&lt;/sup> anions &lt;i>via&lt;/i> inter-molecular N-H⋯O and O-H⋯S hydrogen bonding.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-19T16:20:07.538Z</modification><creation>2025-04-19T16:20:07.538Z</creation></dates><accession>S-EPMC8900515</accession><cross_references><pubmed>35371547</pubmed><doi>10.1107/S2056989022001074</doi></cross_references></HashMap>