| 144030-56-8

• CAS: 144030-56-8
• 化学式: C₂₃H₃₄Cl₂P₂W
• 分子量: 627.226
• InChiKey: ZUSZBSBIZLIZSS-UHFFFAOYSA-L

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
  None
• 环数：
  None
• sp3杂化的碳原子比例：
  None
• 拓扑面积：
  None
• 氢给体数：
  None
• 氢受体数：
  None

反应信息

• 作为产物：
  描述：

  三聚丙烯 、 WCl3(PhC2Ph)(PMe3)2 在 sodium amalgam 作用下， 以 苯 为溶剂， 生成
  参考文献：
  名称：

  The synthesis of octahedral mixed bis-alkyne and alkyne–alkene complexes of tungsten

  摘要：

  用 PhCCPh、PhCCH 和 HCCH 取代 [WCl2(PhC2Ph)(PMe3)3]中的膦配体，或在 MeC2Me 和 Me(CH2)2C2Me 存在下还原 [WCl3(PhC2Ph)(PMe3)2]，可得到混合双炔络合物；在乙烯或丙烯条件下，还原反应生成混合炔烃络合物，[WCl2(PhC2Ph)(CH2CH2)(PMe3)2] 的结构已通过 X 射线晶体学得到证实。

  DOI：

  10.1039/c39920001069

文献信息

• Diphenylacetylene complexes of tungsten containing π-acceptor ligands
  作者：George R. Clark、Alastair J. Nielson、A. David Rae、Clifton E. F. Rickard

  DOI：10.1039/dt9940001783

  日期：——

  Reaction of PhC2Ph with [WCI2(PhC2Ph)(PMe3)3] gave [WCI2(PhC2Ph)2(PMe3)2] 1 for which IR and NMR spectral data indicated cis-chloro ligands. trans phosphines and mutually-cis diphenylacetylene ligands. This geometry was confirmed by X-ray crystallography. The average W-C bond lengths are 2.071 (3) angstrom. The C-13 NMR spectrum showed the acetylenic carbon resonance at delta 185.45. The alkynes HC2H and PhC2H reacted with [WCI2(PhCPh)(PMe3)3] giving [WCl2(PhC2Ph)(HC2H)(PMe3)2] 2 and [WCl2(PhC2Ph)(PhC2H)(PMe3)2] 3. The phenylacetylene ligand gave rise to asymmetry in complex 3 leading to an AB system P-31-H-1} NMR spectrum. Different values of 1J(PW) indicated small differences in the W-P bonding. Alkyl-substituted acetylenes did not react cleanly with [WCl2(PhC2Ph)(PMe3)3]. The complexes [WCl2(PhC2Ph)(PrC2Me)(PMe3)2] 4 and [WCl2(PhC2Ph)(MeC2Me)(PMe3)2] 5 were prepared by sodium-mercury amalgam reduction of [WCl3(PhC2Ph)(PMe3)2] with hex-2-yne or but-2-yne present but were not particularly stable in solution. Sodium-mercury amalgam reduction of [WCI3(PhC2Ph)(PMe3)2] under ethylene or propene gave [WCl2(PhC2Ph)(CH2CH2)(PMe3)2] 6 or [WCI2(PhC2Ph)(MeCHCH2)(PMe3)2] 9. Complex 9 was unstable in solution and was characterised by NMR spectroscopy. The C-13 NMR acetylenic carbon resonances in complexes 6 and 9 are at delta 218.11 and 218.82. Reduction of [WCI3(PhC2Ph)(PMe3)2] under cis- or trans-but-2-ene or 2-methyl propene afforded [WCl2(PhC2Ph)(PMe3)3] and [WCl2(PhC2Ph)(PMe3)2]x 10 as characterised by NMR spectroscopy. Reduction of [WCI3(PhC2Ph)L2] (L = PMe3 or PMePh2) under CO gave [WCI2(PhC2Ph)(CO)(PMe3)2] 11 and [WCl2(PhC2Ph)(CO)(PMePh2)2] 12 for which X-ray crystal structure determinations showed cis-chloro ligands, trans phosphines and mutually-cis PhC2Ph and CO ligands. The W-C and C-C bond lengths for complex 11 are 2.009(5), 2.024(5) and 1.341(6) angstrom, respectively. Overall the reactions showed that the diphenylacetylene ligand in these complexes acts like an organoimido or oxo ligand.