Issue 12, 1982

Sulphur-substituted organotin compounds. Part 8. Preparation and reactions of 3-(p-tolylthio)propyl- and 4-(p-tolylthio)butyl-triphenyltin. Interactions with tetracyanoethylene

Abstract

The reactions of SnPh3[(CH2)nSC6H4Me-p](n= 3 or 4) with mercury(II) chloride, bromine, and iodine lead to phenyl–tin bond cleavage. In contrast, reactions with methyl iodide provide SnPh3[(CH2)nI] and MeSC6H4Me-p. Charge-transfer adducts are formed between SnPh3[(CH2)nSC6H4Me-p](n= 1–4) and tetracyanoethylene or p-bromoanil. The values of λmax. of the complexes indicate similar donor character for SnPh3[(CH2)nSC6H4Me-p](n= 2, 3, or 4); however, the compound SnPh3(CH2SC6H4Me-p) is a stronger donor.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1982, 2321-2326

Sulphur-substituted organotin compounds. Part 8. Preparation and reactions of 3-(p-tolylthio)propyl- and 4-(p-tolylthio)butyl-triphenyltin. Interactions with tetracyanoethylene

J. L. Wardell and J. McM. Wigzell, J. Chem. Soc., Dalton Trans., 1982, 2321 DOI: 10.1039/DT9820002321

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