93122-20-4Relevant articles and documents
SULPHUR-CONTAINING METAL COMPLEXES. PART 9. SYNTHESIS OF TRISUBSTITUTED AMINOCARBENE-THIOETHER CHELATES OF CHROMIUM(0) AND TUNGSTEN(0)
Viljoen, Johanna C.,Lotz, Simon,Linford, Lorna,Raubenheimer, Helgard G.
, p. 1041 - 1046 (2007/10/02)
Several isocyanide-thioether complexes, cis-1)CH2R2>> t, R1R2 = (CH2)3S; R = R1= Ph, R2 = SPh; R = cyclo-C6H11 or CH2Ph, R1R2 = (CH2)3S.M = W: R = But, R1R2 = (CH2)3S> were prepared by u.v. irradiation of the corresponding pentacarbonyl(isocyanide) complexes in the presence of the thioether compounds.Deprotonation of two of these, cis- (M = Cr or W), with LiBu and addition of PEt3, resulted (via consecutive carbonylation and isocyanide insertion into a metal-carbene bond) in the formation of the evasive trisubstituted aminocarbene-thioether chelates, fac-, upon alkylation with .Replacement of the phosphine by 1,3-dithiolane-2-thione under similar reaction conditions yielded, unexpectedly, the substitution products cis (R = But or Ph).When in addition, the isocyanide had been substituted for CO, the first saturated cyclic dithiocarbene complex of chromium, , was formed.