Abstract

The title complex, [Co2(C8H5NO4S)2(C10H8N2)3(H2O)2]·1.3H2O, was synthesized under hydro­thermal conditions. The CoII ion is six-coordinated in a slightly distorted octa­hedral environment resulting from two carboxyl­ate O atoms of two 2-carb­oxy­methyl­sulfanyl nicotinate (2-CMSN2−) anions, one water mol­ecule and three N atoms of three 4,4′-bi­pyridine ligands, with one 4,4′-bi­pyridine ligand situated on a centre of inversion. Two neighboring CoII ions are linked by two anions, giving a dinuclear [Co2(2-CMSN)2] subunit with a Co⋯Co separation of 6.8600 (3) Å. The dinuclear subunits are joined by bridging 4,4′-bi­pyridine linkers, generating a three-dimensional network structure. Disordered water mol­ecules are situated in the free space of this network. O—H⋯O hydrogen bonding within and between the subunits enhances the stability of the structure.

Highlights

  • Zhejiang Key Laboratory for Reactive Chemistry on Solid Surfaces, College of Chemistry and Life Science, Zhejiang Normal University, Jinhua, Zhejiang 321004, People’s Republic of China

  • CoII ion is six-coordinated in a slightly distorted octahedral environment resulting from two carboxylate O atoms of two 2carboxymethylsulfanyl nicotinate (2-CMSN2) anions, one water molecule and three N atoms of three 4,40 -bipyridine ligands, with one 4,40 -bipyridine ligand situated on a centre of inversion

  • Two neighboring CoII ions are linked by two anions, giving a dinuclear [Co2(2-CMSN)2] subunit with a Co Co separation of 6.8600 (3) Å

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Summary

Crystal data

Poly[[diaquatris(l2-4,40 -bipyridine)bis[l2-2-(carboxylatomethylsulfanyl)nicotinato]dicobalt(II)] 1.3-hydrate] Zhejiang Key Laboratory for Reactive Chemistry on Solid Surfaces, College of Chemistry and Life Science, Zhejiang Normal University, Jinhua, Zhejiang 321004, People’s Republic of China Key indicators: single-crystal X-ray study; T = 296 K; mean (C–C) = 0.003 Å; Hatom completeness 94%; disorder in solvent or counterion; R factor = 0.033; wR factor = 0.093; data-to-parameter ratio = 17.3.

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