Structural studies of group 5B–halide–dithio-ligand complexes. Part 6. Crystal structures of dichloro (NN-diethyldithiocarbamato) tris(pyridine)-bismuth(III)–pyridine (1/1) and its di-iodo-analogue

Abstract

Recrystallization of [Bi(S2CNEt2)X2], X = Cl, Br, or I, from pyridine solution has been shown to yield adducts Bi(S2CNEt2)X2(py)4. Single-crystal X-ray structure determinations have shown the three compounds to be isomorphous within a monoclinic unit cell (P21/c) with a ca. 13.7, b ca. 14.4, c ca. 16.0 A, βca. 93–101°, Z= 4, and to comprise [Bi(S2CNEt2)X2(py)3] molecules with a further pyridine solvate molecule in the lattice. The bismuth environment is pseudo-seven-co-ordinate, the pyridine ligands being rather loosely bound, and the stereochemistry pseudo-pentagonal bipyramidal, with axial halogen substituents (Bi–Cl,2.69; Bi–l, 3.06A).