Abstract

The reactions of the metallacyclic complex [Cp(CO) FeC(S)SC(Fp)S ] ( 1) (Cp = η-C 5H 5) with Group IB and IIB metal compounds have been investigated. Electrophilic addition at the thione sulphur atom has been observed in all cases. The reactions of 1 with the coinage metal complexes [MX(PPh 3)] n (M = Cu, X = I, n = 4; M = Ag, X = Cl, n = 4; M = Au, X = Cl, n = 1) in the presence of TlPF 6 give the adducts [Cp(CO) FeC{SM(PPh 3)}SC(Fp)S ]PF 6 ( 2), which have been characterizded spectroscopically. The mercury salt [HgMe]PF 6 reacts similarly with 1 to afford [Cp(CO) FeC(SHgMe)SC(Fp)S ]PF 6 ( 3), whereas mercury dihalides give products that have been shown by an X-ray diffraction study in the case in which X = Br to be halogen-bridged dimers of the type [Cp(CO) FeC(SHgX 2)SC(Fp)S ] 2. The bromine-bridged dimer displays C i symmetry. The coordination around the Hg atoms involves four normal and one weak bonds, and the geometry can be described as a distorted trigonal bipyramid. Zinc chloride reacts with 1 to give an air-sensitive unstable derivative that is tentatively formulated as [Cp(CO) FeC(SZnCl 2)SC(Fp)S ].

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