4-tolyl (16)]. The structure of complex 16 establishes that the bridging 2-C6H4PPh2 group is generated by reduction of the phosphine selenide unit, not by ortho-metallation of the coordinated triphenylphosphine. The chloro-bridges of 5 and 6 are also cleaved by acetylacetonate (acac) and deprotonated Schiff bases forming mononuclear species [Pdκ2-2-C6H4P(X)Ph2}L2] [L2 = acac, X = S (9), Se (10); L2 = 2-OC6H4CHNC6H4-4-R
的治疗[
PTI 2(COD)](COD =
1,5-环辛二烯)与2- LIC 6 ħ 4 P(S)PH 2给出了复杂的顺式- [
铂κ 2 -2-C 6 H ^ 4 P( S)Ph 2 } 2 ](1)含有一对邻
金属化的
三苯基膦硫化物环。
硒对方,[
铂κ 2 -2-C 6 H ^ 4 P(
硒)PH 2 } 2 ](2),它存在如顺式-和反式-异构体在溶液中,将
钯类似物,顺式- [
钯κ 2 -2-C 6 H ^ 4 P(X)PH 2 } 2 ] [X = S(3),
硒(4)],由得到的[的MC1的
金属转移2与
有机锡试剂2-ME(COD)] 3的SnO 6 ħ 4 P(X)PH 2 2摩尔比:在一个1。[PdCl 2(COD)]与2-Me 3 SnC 6 H 4 P(X)Ph 2的摩尔比为1:1,3与
钯的反应(II))
乙酸乙酯,给双核,阴离子桥连的络合物[
钯2(μ-Cl)的2 κ 2 -2-C