[Ni(η²-diphenylacetylene)(1,2-bis(dimethylphosphino)ethane)] | 98316-12-2

• 英文名称: [Ni(η²-diphenylacetylene)(1,2-bis(dimethylphosphino)ethane)]
• 英文别名: [Ni(η²-PhCCPh)(dmpe)]；[Ni(η2-PhC2Ph)(dmpe)]；[Ni(η2-PhC2Ph)(1,2-bis(dimethylphosphino)ethane)]
• CAS: 98316-12-2
• 化学式: C₂₀H₂₆NiP₂
• 分子量: 387.064
• InChiKey: UEHPBIJUAFANLK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
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• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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反应信息

• 作为产物：
  描述：

  、 二苯基乙炔 以 乙醚 为溶剂， 以91%的产率得到[Ni(η²-diphenylacetylene)(1,2-bis(dimethylphosphino)ethane)]
  参考文献：
  名称：

  Poerschke, Klaus R.; Mynott, Richard; Angermund, Klaus, Zeitschrift fur Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1985, vol. 40, # 2, p. 199 - 209

  摘要：

  DOI：

文献信息

• Reaction of an alkyne with dinickel-diphenylsilyl complexes. An emissive disilane formed via the consecutive Si–C and Si–Si bond-making processes
  作者：Makoto Tanabe、Ryouhei Yumoto、Kohtaro Osakada

  DOI：10.1039/c2cc16063c

  日期：——

  [Ni(dmpe)}2(μ-SiHPh2)2] (dmpe = 1,2-bis(dimethylphosphino)ethane) reacted with PhCCPh to yield fluorescent 1,2-bis(E)-1,2-diphenylethenyl}-1,1,2,2-tetraphenyldisilanevia addition of the Si–H bond of the ligand to the alkyne and subsequent coupling of the tertiary silyl ligands forming the Si–Si bond.

  [Ni(dmpe)}2(μ-SiHPh2)2]（dmpe = 1,2-二（二甲基磷基）乙烷）与PhCCPh反应，生成荧光性1,2-二(E)-1,2-二苯乙烯}-1,1,2,2-四苯基二硅烷，该反应通过配体的Si-H键与炔烃的加成以及后续三硅配体的偶联形成Si-Si键。
• Preparation and Properties of Perarylated 3,4-Disila-1,5-hexadienes. A Fluorescent Disilane Accommodated in the Crystal Lattice
  作者：Makoto Tanabe、Ryouhei Yumoto、Kohtaro Osakada、Takanobu Sanji、Masato Tanaka

  DOI：10.1021/om300551t

  日期：2012.10.8

  A dinickel complex with bridging silyl ligands, [Ni(PCy3)}(2)(mu-SiHPh2)(2)] (1), prepared from [Ni(cod)(2)], PCy3, and H2SiPh2, underwent exchange of the PCy3 ligands with 1,2-bis(dimethylphosphino)-ethane (dmpe) to yield a complex coordinated by the two bidentate ligands, [Ni(dmpe)}(2)(mu-SiHPh2)(2)]. Reactions of diarylacetylenes, ArC CAr (Ar = C6H5, C6H4OMe-4, C6H4Me-(4), C6H4F-(4), C6H4CF3-4, C6H4CN-4), with 1 in a 4/1 ratio afforded 1,2-bis(E)-1,2-diarylethenyl}-1,1,2,2-tetraphenyldisilanes via addition of the Si-H bond of the bridging silyl ligand to the alkynes and subsequent coupling of the resulted tertiary silyl ligand. X-ray crystallography of the dialkenyldisilanes resulted in three kinds of conformation of the C=C-Si-Si-C=C chain depending on the aryl group at the vinyl carbon. The disilane with phenyl substituents, 4a (Ar = C6H5), contained a planar C=C-Si-Si-C=C alignment with small Si-Si-C=C torsion angles (1.7(5) and 6.9(5)degrees). The other dialkenyldisilanes, 4b,c,e,f, had much larger torsion angles (30.9(3)-49.2(3)degrees), and the twisted conformation of the molecules was classified into two types. Compound 4a exhibited a fluorescence maximum at 488 nm in the solid state, while 4b f showed peaks at 393-427 nm. The red shift in the emission of 4a is ascribed to orthogonal intramolecular charge transfer (OICT) from the electron-donating Si Si to accepting C=C bonds.