Functionally substituted organotin compounds I. Addition of thiols to alkenyltin compounds
作者:G. Ayrey、R.D. Brasington、R.C. Poller
DOI:10.1016/s0022-328x(00)86887-4
日期:1972.2
3-(Trialkylstannyl)propyl aryl sulphides (R3SnCH2CH2CH2SR′; R = Me, Et, Bu; R′ = Ph, p-tolyl) were prepared by the addition of arenethiols to allyltrialkyltin compounds. Preferential cleavage of the allyl group by the reaction R3SnCH2CHCH2+R′SH→R3SnSR′+CH3CHCH2 occurred when R = R′ = Bu and R = R′ = Ph. Diallyltin dibromide and benzenethiol gave stannous bromide. Mössbauer parameters of the products
通过将芳硫醇加入烯丙基三烷基锡化合物中来制备3-(三烷基锡烷基)丙基芳基硫化物(R 3 SnCH 2 CH 2 CH 2 SR'; R = Me,Et,Bu; R'= Ph,对甲苯基)。烯丙基的优先裂解由反应r 3 SNCH 2 CHCH 2 + R'SH→R 3 SNSR'+ CH 3 CHCH 2发生时R = R'= Bu和R = R'=苯基。Diallyltin二溴化物和苯硫醇制得溴化亚锡。记录产品的Mössbauer参数。