Regioselective versus complete chalcogen transfer reactions of the bis(bidentate) phosphine cis,trans,cis-1,2,3,4-tetrakis(diphenylphosphino)cyclobutane: full characterization of new, hemilabile ligands and their complexes with palladium(<scp>ii</scp>) and platinum(<scp>ii</scp>)
作者:Thomas Stampfl、Rene Gutmann、Georg Czermak、Christoph Langes、Alexander Dumfort、Holger Kopacka、Karl-Hans Ongania、Peter Brüggeller
DOI:10.1039/b305775e
日期:——
The bis(bidentate) phosphine cis,trans,cis-1,2,3,4-tetrakis(diphenylphosphino)cyclobutane (dppcb) has been regioselectively oxidized by sulfur to the novel, hemilabile disulfide cis,trans,cis-2,3-bis(diphenylphosphinothioyl)-1,4-bis(diphenylphosphino)cyclobutane (2,3-trans-dppcbS2, I). Also the tetrachalcogenides cis,trans,cis-1,2,3,4-tetrakis(diphenylphosphinoyl)cyclobutane (dppcbO4, II), cis,trans
之二 膦顺,反式,顺式-1,2,3,四(
二苯基膦)环(dppcb)已被
硫区域选择性氧化为新颖的,半不稳定的二
硫键顺式,反式,顺式-2,3-双(
二苯基膦硫基)-1,4-双(
二苯基膦基)
环丁烷(2,3-反式-dppcbS 2,I)。还有四
硫属元素化物顺,反,顺-1,2,3,4-四(
二苯基膦酰基)
环丁烷(dppcbO 4,II),顺式,反式,顺式-1,2,3,4-四(
二苯基膦硫基)
环丁烷(dppcbS 4,III)和顺式,反式,顺式-1,2,3,4-四(
二苯基膦基硒酰基)
环丁烷(dppcbSe 4,IV)已获得。先前制备的二
硫化物顺,反,顺-1,3-双(
二苯基膦硫基)-2,4-双(
二苯基膦基)
环丁烷(1,3-反-dppcbS 2)的区域选择性
硒化导致独特的混合
硫族化物顺式,反式,顺式-1,3-双(
二苯基膦基硒酰基)-2,4-双(
二苯基膦硫基)
环丁烷(反式-dppcbSe 2 S 2,V)。所有新的
配体