Abstract
The interaction of carbon disulphide with triphenylphosphine complexes of Ni, Pd, Pt, Rh, and Ir in zero or +1 oxidation states leads to complexes in which the CS2 ligand is “π-bonded”, as exemplified by the first member of this new class of compound whose structure has been confirmed by crystallographic methods, bis(triphenylphosphine)(carbon disulphide)platinum(II). Evidence for a donor complex of CS2 has been obtained in one case. Structurally related “π-complexes” have been obtained from carbonyl sulphide, and alkyl and aryl isothiocyanates. An allyl isothiocyanate–platinum complex is best formulated with metal-bonded π-allyl and thiocyanato-groups, however. In the interaction of the isothiocyanates with tris(triphenylphosphine)chlororhodium(I), both “π-bonded” and donor co-ordinated isothiocyanates are present. A π-perfluorothioacetone complex (Ph3P)2Pt(C2F6CS) and a benzoyl complex (Ph3P)2PtCl(COPh) are obtained from the interaction of Pt(PPh3)3 with 2,2,4,4-tetrakis(trifluoromethyl)-1,3-dithietan and benzoyl chloride, respectively; also described is the arylazo-complex RhCl2(p-FC6H4N2)(PPh3)2, 0·5CHCl3, obtained by interaction of para-fluorophenyldiazonium tetrafluoroborate with RhCl2H(PPh3)2.