首页> 外文期刊>Journal of chemical crystallography >Synthesis and crystal structure of [WI(CO)(cis-dppen)(#eat#~2-MeC_2Me)_2]I centre dot CH_2Cl_2 {cis-dppen = bis(diphenylphosphino)ethene}
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Synthesis and crystal structure of [WI(CO)(cis-dppen)(#eat#~2-MeC_2Me)_2]I centre dot CH_2Cl_2 {cis-dppen = bis(diphenylphosphino)ethene}

机译:[WI(CO)(cis-dppen)(#eat#〜2-MeC_2Me)_2] I中心点CH_2Cl_2的合成与晶体结构{cis-dppen = bis(diphenylphosphino)ethene}

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摘要

The complex [WI(CO)(cis-dppen)(#eta#~2-MeC_2Me)_2]I centre dot CH_2Cl_2(1) is prepared as a by-product from the reaction of equimolar quantities of [WI_2(CO)(NCMe)(#eta#~2-MeC_2Me)_2] and cis-dppen {dppen = bis(diphenylphosphino)ethene}. Complex 1, [WI(CO)(cis-dppen)(#eta#~2-MeC_2Me)_2]I centre dot CH_2Cl_2 crystallizes in the triclinic space group P1-bar with a = 11.189(13), b = 12.331(14), c = 15.395(17) A, #alpha# = 83.61(1), #beta# = 86.06(1), #gamma# = 64.48(1) deg, U = 1904 A~3, and Z = 2. The metal environment in the cation can best be considered as a distorted octahedron with the two but-2-yne groups taking up individual sites trans to phosphorus atoms of the dppen ligand. The coordination sphere is completed by mutually trans-carbonyl and iodide groups.
机译:[WI(CO)(cis-dppen)(#eta#〜2-MeC_2Me)_2] I中心点CH_2Cl_2(1)由等摩尔量的[WI_2(CO)( NCMe)(#eta#〜2-MeC_2Me)_2]和顺式-dppen {dppen =双(二苯基膦基)乙烯}。配合物1,[WI(CO)(cis-dppen)(#eta#〜2-MeC_2Me)_2] I中心点CH_2Cl_2在三斜空间群P1-bar中结晶,a = 11.189(13),b = 12.331(14) ),c = 15.395(17)A,#alpha#= 83.61(1),#beta#= 86.06(1),#gamma#= 64.48(1)度,U = 1904 A〜3,Z = 2。阳离子中的金属环境最好被认为是扭曲的八面体,其中的两个丁-2-炔基占据了可逆于dppen配体的磷原子的单个位点。配位球由相互的反羰基和碘化物基团完成。

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