<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>68(Pt 4)</volume><submitter>Schell AC</submitter><pubmed_abstract>In the title coordination polymer, [Pb(C(5)H(9)NO(2)S)](n) {systematic name: catena-poly[(μ-2-amino-3-methyl-3-sulfido-butano-ato)lead(II)]}, the d-penicillaminate ligand coordin-ates to the metal ion in an N,S,O-tridentate mode. The S atom acts as a bridge to two neighbouring Pb(II) ions, thereby forming a double thiol-ate chain. Moreover, the coordinating carboxyl-ate O atom forms bridges to the Pb(II) ions in the adjacent chain. The overall coordination sphere of the Pb(II) ion can be described as a highly distorted penta-gonal bipyramid with a void in the equatorial plane between the long Pb-S bonds probably occupied by the stereochemically active inert electron pair. The amino H atoms form N-H⋯S and N-H⋯O hydrogen bonds, resulting in a cluster of four complex units, giving rise to an </pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>m489-90</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3343873</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Redetermination of (d-penicillaminato)lead(II).</pubmed_title><pmcid>PMC3343873</pmcid><pubmed_authors>Parvez M</pubmed_authors><pubmed_authors>Schell AC</pubmed_authors><pubmed_authors>Jalilehvand F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Redetermination of (d-penicillaminato)lead(II).</name><description>In the title coordination polymer, [Pb(C(5)H(9)NO(2)S)](n) {systematic name: catena-poly[(μ-2-amino-3-methyl-3-sulfido-butano-ato)lead(II)]}, the d-penicillaminate ligand coordin-ates to the metal ion in an N,S,O-tridentate mode. The S atom acts as a bridge to two neighbouring Pb(II) ions, thereby forming a double thiol-ate chain. Moreover, the coordinating carboxyl-ate O atom forms bridges to the Pb(II) ions in the adjacent chain. The overall coordination sphere of the Pb(II) ion can be described as a highly distorted penta-gonal bipyramid with a void in the equatorial plane between the long Pb-S bonds probably occupied by the stereochemically active inert electron pair. The amino H atoms form N-H⋯S and N-H⋯O hydrogen bonds, resulting in a cluster of four complex units, giving rise to an </description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Apr</publication><modification>2025-04-04T09:12:17.892Z</modification><creation>2019-03-27T00:53:02Z</creation></dates><accession>S-EPMC3343873</accession><cross_references><pubmed>22589847</pubmed><doi>10.1107/S1600536812011877</doi></cross_references></HashMap>