and 1,4-phenylene distibines, 1,3-C6H4(SbMe2)2 and 1,4-C6H4(SbMe2)2, were made similarly. The new ligands have been characterised by mass spectrometry, 1H and 13C[1H] NMR spectroscopy, and by the preparation of methiodide derivatives. The crystal structures of 1,4-C6H4(CH2SbMe2)2 and [1,3-C6H4(CH2SbMe3)2]I2 have been determined. The synthesis of 1,2-C6H4(CH2SbPh2)2 has been achieved similarly in modest
高产率合成1,2-,1,3-和1,4-二
甲苯基二
异戊二烯(1,2-
C6H4(CH2SbMe2)2、1,3- (CH2SbMe2)2、1,4- (CH2SbMe2)报告了分别由Me2SbCl(方便地由Me2PhSb和HCl气体原位制得)和适当的di-Grignard制得的。类似地制备1,3-和1,4-亚苯基二甲
苯二胺1,3-C 6 H 4(SbMe 2)2和1,4-C 6 H 4(SbMe 2)2。通过质谱,1H和13C [1H] NMR光谱,以及通过制备甲
硫醚衍
生物,对新的
配体进行了表征。已经确定了1,4- (CH2SbMe2)2和[1,3- (CH2SbMe3)2] I2的晶体结构。相似地,以适度的产率完成了1,2- (CH2SbPh2I2)2的合成,并且二苯乙啶转化为四
碘衍
生物的1,2- (CH2SbPh2I2)2。这些
配体可利用的配位模式已通过与
镍