<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>74(Pt 6)</volume><submitter>Ndoye C</submitter><funding>Sonatel Foundation</funding><pubmed_abstract>The binuclear complex, [Sn&lt;sub>2&lt;/sub>(C&lt;sub>4&lt;/sub>H&lt;sub>9&lt;/sub>)&lt;sub>4&lt;/sub>(C&lt;sub>16&lt;/sub>H&lt;sub>10&lt;/sub>N&lt;sub>4&lt;/sub>O&lt;sub>4&lt;/sub>)], contains two Sn&lt;sup>4+&lt;/sup> ions, connected by doubly N-deprotonated oxalylbis[(2-oxido-benzyl-idene)hydrazide] ligands, and each Sn&lt;sup>4+&lt;/sup> ion is linked to two &lt;i>tert&lt;/i>-butyl groups. The coordination sphere of each Sn atom is best described as a distorted trigonal bipyramid. Each stannic ion in the complex is in a C&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>N environment. The two homologous parts of the doubly deprotonated ligand are located in &lt;i>trans&lt;/i> positions with respect to the C-C bond of the oxalamide group. The oxalamide group exhibits an asymmetric coordination geometry, as seen by the slight difference between the C-O and C-N bond lengths. The thre</pubmed_abstract><journal>Acta crystallographica. Section E, Crystallographic communications</journal><pagination>799-802</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6002830</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Crystal structure of (μ-&lt;i>trans&lt;/i>-1,2-bis-{2-[(2-oxido-phen-yl)methyl-idene]hydrazin-1-yl-idene}ethane-1,2-diolato-κ&lt;sup>3&lt;/sup>&lt;i>O&lt;/i>,&lt;i>O&lt;/i>',&lt;i>N&lt;/i>)bis-[di-&lt;i>tert&lt;/i>-butyl-tin(IV)].</pubmed_title><pmcid>PMC6002830</pmcid><pubmed_authors>Gautier R</pubmed_authors><pubmed_authors>Diallo W</pubmed_authors><pubmed_authors>Gaye M</pubmed_authors><pubmed_authors>Ndoye C</pubmed_authors><pubmed_authors>Diouf O</pubmed_authors><pubmed_authors>Barry AH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Crystal structure of (μ-&lt;i>trans&lt;/i>-1,2-bis-{2-[(2-oxido-phen-yl)methyl-idene]hydrazin-1-yl-idene}ethane-1,2-diolato-κ&lt;sup>3&lt;/sup>&lt;i>O&lt;/i>,&lt;i>O&lt;/i>',&lt;i>N&lt;/i>)bis-[di-&lt;i>tert&lt;/i>-butyl-tin(IV)].</name><description>The binuclear complex, [Sn&lt;sub>2&lt;/sub>(C&lt;sub>4&lt;/sub>H&lt;sub>9&lt;/sub>)&lt;sub>4&lt;/sub>(C&lt;sub>16&lt;/sub>H&lt;sub>10&lt;/sub>N&lt;sub>4&lt;/sub>O&lt;sub>4&lt;/sub>)], contains two Sn&lt;sup>4+&lt;/sup> ions, connected by doubly N-deprotonated oxalylbis[(2-oxido-benzyl-idene)hydrazide] ligands, and each Sn&lt;sup>4+&lt;/sup> ion is linked to two &lt;i>tert&lt;/i>-butyl groups. The coordination sphere of each Sn atom is best described as a distorted trigonal bipyramid. Each stannic ion in the complex is in a C&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>N environment. The two homologous parts of the doubly deprotonated ligand are located in &lt;i>trans&lt;/i> positions with respect to the C-C bond of the oxalamide group. The oxalamide group exhibits an asymmetric coordination geometry, as seen by the slight difference between the C-O and C-N bond lengths. The thre</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jun</publication><modification>2026-07-08T03:17:12.258Z</modification><creation>2019-03-26T23:43:33Z</creation></dates><accession>S-EPMC6002830</accession><cross_references><pubmed>29951233</pubmed><doi>10.1107/S2056989018007077</doi></cross_references></HashMap>