{W(CO)4(η5-7,8-Me2-7,8-C2B9H8-10-CH2C6H4Me-4)} | 138923-80-5

• 英文名称: {W(CO)4(η5-7,8-Me2-7,8-C2B9H8-10-CH2C6H4Me-4)}
• CAS: 138923-80-5
• 化学式: C₁₆H₂₃B₉O₄W
• 分子量: 560.505
• InChiKey: ZHQNNNGLHDVJJR-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

• 作为反应物：
  描述：

  {W(CO)4(η5-7,8-Me2-7,8-C2B9H8-10-CH2C6H4Me-4)} 、 四乙基氯化铵一水合物 以 四氢呋喃 为溶剂， 以96%的产率得到{Et4N}{closo-1,8-Me2-11-(CH2C6H4Me-4)-2-chloro-2,2,2-(carbonyl)3-2,1,8-tungstacarborane}
  参考文献：
  名称：

  Brew, Stephen A.; Carr, Nicholas; Jeffery, John C., Journal of the American Chemical Society, 1992, vol. 114, # 6, p. 2203 - 2210

  摘要：

  DOI：
• 作为产物：
  描述：

  {PPh4}{closo-1,8-Me2-11-(CH2C6H4Me-4)-2-I-2,2,2-(CO)3-2,1,8-WC2B9H8} 在 CO 、 AgBF₄ 作用下， 以 二氯甲烷 为溶剂， 以42%的产率得到{W(CO)4(η5-7,8-Me2-7,8-C2B9H8-10-CH2C6H4Me-4)}
  参考文献：
  名称：

  Brew, Stephen A.; Carr, Nicholas; Jeffery, John C., Journal of the American Chemical Society, 1992, vol. 114, # 6, p. 2203 - 2210

  摘要：

  DOI：

文献信息

• Alkylidyne(carbaborane) complexes of the Group 6 metals. Part 1. Proton-induced alkylidyne ligand migration
  作者：Stephen A. Brew、David D. Devore、Paul D. Jenkins、Massimino U. Pilotti、F. Gordon A. Stone

  DOI：10.1039/dt9920000393

  日期：——

  Treatment of carbon monoxide-saturated solutions of the salts [NEt4][W(= CR)(CO)2(eta(5)-C2B9H9Me2)] (R = C6H4Me-4 or Me) at ca. -78-degrees-C with HBF4.Et2O affords the complexes [W(CO)4eta(5)-C2B9H8(CH2R)Me2}]. If these protonation reactions are carried out in the presence of PhC = CPh, the alkynetungsten complexes [W(CO)(PhC2Ph)2eta(5)-C2B9H8(CH2R)Me2}] are formed via the intermediacy of dicarbonyl species [W(CO)2(PhC2Ph)2eta(5)-C2B9H8(CH2R)Me2}]. The latter (R = C6H4Me-4) with PMe3 yields the compound [W(CO)(PMe3)(PhC2Ph)eta(5)-C2B9H8(CH2C6H4Me-4)Me2}]. Treatment of [NEt4][W(= CC6H4Me-4) (CO)2(eta(5)-C2B9H9Me2)] with HBF4.Et2O in the presence of CNBut yields [W(CO)2(CNBut)2eta(5)-C2B9H8(CH2C6H4Me-4)Me2}], whereas if PPh3 is used instead of CNBut a tricarbonyl species [W(CO)3(PPh3)eta(5)-C2B9H8(CH2C6H4Me-4)Me2}] is isolated. However, the latter disproportionates in solution to afford the bis(triphenylphosphine) complex [W(CO)2(PPh3)2eta(5)-C2B9H8(CH2C6H4Me-4)Me2}], crystals of which have been analysed by X-ray crystallography. The tungsten atom is eta(5) co-ordinated by the C2B9H8(CH2C6H4Me-4)Me2 ligand and is ligated by two CO and two PPh3 groups, having transoid arrangements. The CH2C6H4Me-4 substituent on the cage is bonded to the boron atom which is in the beta-site with respect to the two carbons in the open pentagonal activated CCBBB face of the nido-icosahedral C2B9 fragment. This geometry accounts for the NMR data (H-1, C-13-H-1} and B-11-H-1} for all the new complexes reported containing the C2B9H8(CH2R)Me2 cage system.
• Carr, Nicholas; Mullica, Donald F.; Sappenfield, Eric L., Organometallics, 1992, vol. 11, # 11, p. 3697 - 3704
  作者：Carr, Nicholas、Mullica, Donald F.、Sappenfield, Eric L.、Stone, F. Gordon A.

  DOI：——

  日期：——