Issue 14, 1992

Reactivity of co-ordinated S2CPR3 ligands. Crystal and molecular structure of [Mo{η3-SC(SMe)PMe3}(CO)2(PMe3)2]I

Abstract

Treatment of [Mo(S2CPMe3)(CO)2(PMe3)2]1 with HBF4 or RI affords respectively [Mo{S2C(H)PMe3}(CO)2(PMe3)2]BF42 and [Mo{η3-SC(SR)PMe3}(CO)2(PMe3)2]I (R = Me 3a or Et 3b); an X-ray study of 3a shows that alkylation takes place at sulfur and that the resulting phosphoniodithioester ligand is trihapto (S,S′,C) bonded to molybdenum.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1992, 2307-2308

Reactivity of co-ordinated S2CPR3 ligands. Crystal and molecular structure of [Mo{η3-SC(SMe)PMe3}(CO)2(PMe3)2]I

A. Galindo, E. Gutiérrez-Puebla, A. Monge, M. A. Muñoz, A. Pastor, C. Ruiz and E. Carmona, J. Chem. Soc., Dalton Trans., 1992, 2307 DOI: 10.1039/DT9920002307

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