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Synthesis, characterization and structures of cadmium(II) and mercury(II) complexes with bis(dipiperidinylphosphino)methylamine dichalcogenides

机译:双(二哌啶基膦基)甲胺二卤化镉(II)和汞(II)配合物的合成,表征和结构

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摘要

Two new bidentate phosphine dichalcogenide ligands of the type MeN(PipPE) [(Pip = piperidinyl; E = S () or Se ()] and their cadmium(II) and mercury(II) chloride complexes MCl{MeN(PipPE)} [M = Cd; E = S (); Se () or M = Hg; L = S (); Se ()] were prepared and characterized by elemental analysis, IR, multinuclear (P, Se and Cd) NMR spectroscopy and single crystal X-ray analyses. Ligands and were found to adopt anti conformation structures in the solid state in which both P=E groups are trans to each other. Complexes - are comprised of one ligand coordinated in a bidentate fashion to the metal centre in a distorted tetrahedral arrangement [98.46(3)-121.24(4)°]. The P=S bond lengths of 1.999(15)-2.003(14) Å in the complex () are slightly elongated compared to those in free ligand [1.933(15)-1.950(14) Å]. The results are discussed and compared with closely related analogues.
机译:MeN(PipPE)类型的两个新的双齿膦二硫代膦配体[[Pip =哌啶基; E = S()或Se()]以及它们的氯化镉和氯化汞配合物MCl {MeN(PipPE)} [ M = Cd; E = S(); Se()或M = Hg; L = S(); Se()]的制备和表征通过元素分析,IR,多核(P,Se和Cd)NMR光谱和单原子晶体和X射线分析发现,配体和处于固态的反构象结构,其中两个P = E基团彼此互反。配合物-由一个配体组成,该配体以双齿的方式与金属中心形成双键配位。扭曲的四面体排列[98.46(3)-121.24(4)°。与自由配体[1.933(15)-2]中的1.999(15)-2.003(14)Å相比,复合物()中的P = S键长略长15)-1.950(14)Å]。对结果进行了讨论,并与密切相关的类似物进行了比较。

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