MAIN-GROUP METAL HALIDE-COMPLEXES WITH STERICALLY HINDERED THIOUREAS .15. THE CRYSTAL AND MOLECULAR-STRUCTURES OF 2 UNIQUE MONOMERIC BISMUTH(III) THIOCYANATE COMPLEXES WITH 1,3-DIMETHYL-2(3H)-IMIDAZOLETHIONE
Dj. Williams et al., MAIN-GROUP METAL HALIDE-COMPLEXES WITH STERICALLY HINDERED THIOUREAS .15. THE CRYSTAL AND MOLECULAR-STRUCTURES OF 2 UNIQUE MONOMERIC BISMUTH(III) THIOCYANATE COMPLEXES WITH 1,3-DIMETHYL-2(3H)-IMIDAZOLETHIONE, Inorganica Chimica Acta, 228(2), 1995, pp. 69-72
Two new bismuth(III) thiocyanate complexes with a sterically hindered
thiourea, 1,3-dimethyl-2(3H)-imidazolethione (dmit), have been prepare
d and characterized via X-ray crystallography and IR spectroscopy. One
complex, [Bi(S)NCS(dmit)(3)]. 2H(2)O (I), could not be obtained in an
alytically pure form, but an individual crystal reveals a slightly dis
torted octahedral structure With one of the water molecules occupying
the position trans to the sulfide group. The other complex, [Bi(SCN)(N
CS),(dmit)(3)] (II), was also a distorted octahedral with the dmit lig
ands in a meridional configuration, Two of the thiocyanates are N-bond
ed and the other is S-bonded. IR spectra show characteristic thiocyana
te CN stretches correlating to the bonding mode for both complexes, an
d neither complex shows strong evidence of a stereoactive lone pair.