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.