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Redetermination of (d-penicillaminato)lead(II)
Adam C Schell1, Masood Parvez, Farideh Jalilehvand
1Department of Chemistry, The University of Calgary, 2500 University Drive NW, Calgary, Alberta, Canada T2N 1N4.
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 R(4) (4)(16) ring lying in the ab plane. The crystal structure of the title compound has been reported previously [Freeman et al. (1974 ▶). Chem. Soc. Chem. Commun. pp. 366-367] but the atomic coordinates have not been deposited in the Cambridge Structural Database (refcode DPENPB). Additional details of the hydrogen bonding are presented here.
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