<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>68(Pt 5)</volume><submitter>Fonseca Ade S</submitter><pubmed_abstract>The reaction of cadmium acetate dihydrate with 2-acetyl-pyridine (4-phenyl-thio-semicarbazone) yielded the title compound, [Cd(C(14)H(13)N(4)S)(2)]. The Cd(II) atom is six-coordin-ated in a distorted octa-hedral environment by two deproton-ated thio-semicarbazone ligands acting in a tridentate chelating mode through two N and one S atoms, forming metalla-rings. In the crystal, mol-ecules are connected through inversion centers via pairs of N-H⋯S inter-actions, building a one-dimensional hydrogen-bonded polymer along [0-1-1].</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>m635-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3344363</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Bis{4-phenyl-1-[1-(pyridin-2-yl-κN)ethyl-idene]thio-semicarbazidato-κ(2)N(1),S}cadmium.</pubmed_title><pmcid>PMC3344363</pmcid><pubmed_authors>Fonseca Ade S</pubmed_authors><pubmed_authors>Gervini VC</pubmed_authors><pubmed_authors>Bresolin L</pubmed_authors><pubmed_authors>de Oliveira AB</pubmed_authors><pubmed_authors>Locatelli A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bis{4-phenyl-1-[1-(pyridin-2-yl-κN)ethyl-idene]thio-semicarbazidato-κ(2)N(1),S}cadmium.</name><description>The reaction of cadmium acetate dihydrate with 2-acetyl-pyridine (4-phenyl-thio-semicarbazone) yielded the title compound, [Cd(C(14)H(13)N(4)S)(2)]. The Cd(II) atom is six-coordin-ated in a distorted octa-hedral environment by two deproton-ated thio-semicarbazone ligands acting in a tridentate chelating mode through two N and one S atoms, forming metalla-rings. In the crystal, mol-ecules are connected through inversion centers via pairs of N-H⋯S inter-actions, building a one-dimensional hydrogen-bonded polymer along [0-1-1].</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 May</publication><modification>2025-04-04T14:12:37.42Z</modification><creation>2019-03-27T00:53:05Z</creation></dates><accession>S-EPMC3344363</accession><cross_references><pubmed>22590129</pubmed><doi>10.1107/S1600536812016558</doi></cross_references></HashMap>