
Journal of Organometallic Chemistry p. 79 - 92 (1990)
Update date:2022-08-02
Topics:
Sanchez-Pelaez, A.E.
Perpinan, M.F.
Gutierrez-Puebla, E.
Monge, A.
Ruiz-Valero, C.
The reactions of the zerovalent carbonyl complexes, M(CO)6, M(CO)5(Rpy), M(CO)4(Rpy)2 (M = Mo, W, R = 2-Me, H) with a series of potentially mono- or bi-dentate uninegative (S,X)-donor ligands (S,X = xanthates, dithiocarbamates, pyridine-2-thiol, P,P-diphenyl-N-phenylphosphinothioformomido, P,P-diphenylphosphinedithioformamide) have given two types of anionic complexes; a mono- or bi-dentate group, respectively, were isolated as their tetraphenylphosphonium or triethylammonium salts.Reactions of some of these species with allyl bromide and HgX2 are described.The crystal structure of a 14.555(4), b 12.44(1), c 17.950(2) Angstroem, U 3145.9(3) Angstroem3, Z = 4; Dc 1.65 g cm-3, μ(Mo-Kα) 39.68 cm-1, F(000) = 1544, R = 0.042 for 4278 observed reflections.In this complex the xanthate ligand is monodentate.
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