首页> 中文期刊> 《无机化学学报》 >金属配合物MBr{(Ph2PCH2CH2)2C6H3),M=Pd(Ⅱ)、Pt(Ⅱ)的合成及晶体结构

金属配合物MBr{(Ph2PCH2CH2)2C6H3),M=Pd(Ⅱ)、Pt(Ⅱ)的合成及晶体结构

         

摘要

A new diphosphine ligand, 2, 6-bis (diphenylphosphinoethyl) bromobenzene, was synthesized and two new complexes , [PdBr{ (Ph2PCH2CH2)2C6H3} ] (1) and [PtBr{ (Ph2PCH2CH2)2C6H3} ] (2), were obtained by the oxidative addition reaction of Pd0(DBA)2(DBA is PhHC = CHCOCH = CHPh) and Pt0(PPh3) 4 with this ligand, respectively. The two complexes were characterized by 31p NMR, 1H NMR and X-ray diffraction. The crystallographic data of complex (1) are: space group Pna21, a = 16. 806(2)A, b=18.578(2)A, c =9.643(5)A and these of complex (2) are: space group P21/a, a=12.364(3)A, b=17.676(4)A, c=13.672(7)A, β=94.8b(3)°.%合成了一个新的双膦配位体:2,6-双(二苯基膦乙基)溴苯,通过Pd0(DBA)2,(DBA为PhHC=CHCOCH=CHPh),pt0(PPh3)4和该配位体的氧化加成反应,分别得到了两个新的金属配合物:rn[PdBr{(pH2PCH2CH2)2C6H3}](1)和[PtBr{(Ph2PCH2CH2)2C6H3}](2),并进行了31P NMR,1H NMR的表征。通过X-[PdBr{(pH2PCH2CH2)2C6H3}](1)和[PtBr{(Ph2PCH2CH2)2C6H3}](2),并进行了31P NMR,1H NMR的表征。通过X-射线晶体结构测定,这两个配合物的晶体学参数分别为:配合物(1)的晶体属正交晶系,空间群Pna21,a=16.806(2)A,b=18.578(2)A,c=9.643(5)A;配合物(2)的晶体属单斜晶系,空间群P21/a,α=12.364(3) ,b=17.676(4)A,c=13.672(7)A,β=94.86(3)°。

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