[(1,1,1-tris(diphenylphosphinomethyl)ethane)Ir(C2H4)(H)2]BPh4 | 134882-83-0

• 英文名称: [(1,1,1-tris(diphenylphosphinomethyl)ethane)Ir(C2H4)(H)2]BPh4
• 英文别名: {(triphos)Ir(H)2(C2H4)}BPh4
• CAS: 134882-83-0
• 化学式: C₂₄H₂₀B*C₄₃H₄₅IrP₃
• 分子量: 1166.21
• InChiKey: YKCTUCKYFONVEL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 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：

  [(1,1,1-tris(diphenylphosphinomethyl)ethane)Ir(C2H4)(H)2]BPh4 在 氢气 作用下， 以 neat (no solvent) 为溶剂， 以100%的产率得到{(triphos)IrH(μ-H)2HIr(triphos)}(BPh4)2
  参考文献：
  名称：

  三足（聚膦）金属配合物的分子固态有机金属化学。乙烯在铱催化加氢

  摘要：

  [(triphos)Ir(H) 2 (C 2 H 4 )]BPh 4 (1) 与 CO、C 2 H 4 和 H 2 的固-气反应描述为 [triphos=MeC(CH 2 PPh 2 ) 3]。气态反应物促进从 1 中消除乙烷并形成 [(triphos)Ir(CO) 2 ]BPh 4 、[(triphos)Ir(C 2 H 4 ) 2 )BPh 4 和 [(triphos)Ir( H) 2 ]BPh 4 ，分别。后一种 16 电子物种在低于 70 o C 的温度下以固态分离

  DOI：

  10.1021/ja00058a021
• 作为产物：
  描述：

  在 一氧化碳 作用下， 以 neat (no solvent) 为溶剂， 以>99的产率得到[(1,1,1-tris(diphenylphosphinomethyl)ethane)Ir(C2H4)(H)2]BPh4
  参考文献：
  名称：

  三足（聚膦）金属配合物的分子固态有机金属化学。乙烯在铱催化加氢

  摘要：

  [(triphos)Ir(H) 2 (C 2 H 4 )]BPh 4 (1) 与 CO、C 2 H 4 和 H 2 的固-气反应描述为 [triphos=MeC(CH 2 PPh 2 ) 3]。气态反应物促进从 1 中消除乙烷并形成 [(triphos)Ir(CO) 2 ]BPh 4 、[(triphos)Ir(C 2 H 4 ) 2 )BPh 4 和 [(triphos)Ir( H) 2 ]BPh 4 ，分别。后一种 16 电子物种在低于 70 o C 的温度下以固态分离

  DOI：

  10.1021/ja00058a021

文献信息

• Barbara, Pierluigi; Bianchini, Claudio; Meli, Andrea, Organometallics, 1991, vol. 10, # 7, p. 2227 - 2238
  作者：Barbara, Pierluigi、Bianchini, Claudio、Meli, Andrea、Peruzzini, Maurizio、Vacca, Alberto、Vizza, Francesco

  DOI：——

  日期：——
• Mechanistic Study of Ir(H)2-Assisted Transformations of Ethyne: Cyclotrimerization, Cooligomerization with Ethene, and Reductive Coupling
  作者：Claudio Bianchini、Kenneth G. Caulton、Todd J. Johnson、Andrea Meli、Maurizio Peruzzini、Francesco Vizza

  DOI：10.1021/om00002a046

  日期：1995.2

  The (ethene)dihydride complex [(triphos)Ir(H)(2)(C2H4)]BPh(4) (1) is capable of promoting a variety of transformations of ethyne, including cyclotrimerization to benzene, cooligomerization with ethene to hexa-1,3,5-triene, reductive coupling to buta-1,3-diene, and hydrogenation to ethene (triphos = MeC(CH(2)PPh(2))(3)). A detailed study under various experimental conditions, the detection of several intermediates along the various reaction paths, and the use of isolated complexes in independent reactions, taken together, permit mechanistic conclusions that account for the varied products. In particular, the cyclotrimerization and cooligomerization reactions are mediated by an iridacyclopentadiene species which is trapped by either ethyne or ethene. Consumption of the hydride ligands of 1 by C2H2 or C2H4 is an ingredient for both cyclotrimerization and cooligomerization reactions but is not. necessary to accomplish the reductive dimerization of ethyne to buta-1,3-diene for which, conversely, the two hydride ligands are mandatory.
• Molecular Solid-Gas Organometallic Chemistry. Catalytic and Stoichiometric Iridium-Assisted C-C Bond-Forming Reactions Involving Ethyne and Ethene
  作者：Claudio Bianchini、Mauro Graziani、Jan Kaspar、Andrea Meli、Francesco Vizza

  DOI：10.1021/om00016a020

  日期：1994.4

  Treatment of crystals of the (eta2-ethene)dihydride complex [(triphos)Ir(H)2(C2H4)]BPh4 (1; triphos = MeC(CH2PPh2)3) with ethyne (4 atm) at 70-degrees-C for 3 h results in evolution of ethene and but-2-ene and formation of five different organometallic products, namely the eta4-benzene complex [(triphos)Ir(eta4-C6H6)]BPh4 (2), the eta4-buta-1,3-diene complex [(triphos)Ir(eta4-C4H6)]BPh4 (3), the eta4-cyclohexa-1,3-diene complex [(triphos)Ir(eta4-C6H8)]BPh4 (4), and the crotyl hydride isomers [(triphos)Ir(H) (eta3-MeC3H4)]BPh4 (5-anti and 5-syn) in a kinetic product ratio of 35:5:23:28:9. At 100-degrees-C, the solid-gas reaction produces catalytic amounts of benzene, the catalyst precursor being the eta4-benzene complex 2. Temperature-programmed reactions carried out in a flow reactor and the use of isolated complexes in independent solid-gas reactions permit mechanistic conclusions which account for the varied organic and organometallic products. The ethene ligand in 1 is an essential ingredient for both cyclotrimerization and cooligomerization reactions of ethyne, which are traversed by eta3-crotyl complexes. Conversely, the ethene ligand is a competitive inhibitor for the reductive dimerization of ethyne to buta-1,3-diene, for which the two hydride ligands are mandatory. Comparison with fluid solution-phase systems provides evidence for the control exerted by the constraining environment of the crystal lattice on the solid-gas reactions.
• Bianchini, Claudio; Moneti, Simonetta; Peruzzini, Maurizio, Inorganic Chemistry, 1997, vol. 36, # 25, p. 5818 - 5825
  作者：Bianchini, Claudio、Moneti, Simonetta、Peruzzini, Maurizio、Vizza, Francesco

  DOI：——

  日期：——
• Molecular solid-gas organometallic chemistry. Catalytic and stoichiometric transformations of ethyne at iridium
  作者：Claudio Bianchini、Piero Frediani、Mauro Graziani、Jan Kaspar、Andrea Meli、Maurizio Peruzzini、Francesco Vizza

  DOI：10.1021/om00032a006

  日期：1993.8

  The eta2-ethene dihydride [(triphos)Ir(H)2-(C2H4)]BPh4 (1; triphos = MeC(CH2PPh2)3) reacts in the solid state with ethyne (4 atm) at 70-degrees-C to give five different organometallic products, namely [(triphos)-Ir(eta4-C6H6)]BPh4 (2), [(triphos)Ir(eta4-C6H8)]BPh4 (3), [(triphos)Ir(eta4-C4H6)]BPh4 (4), [(triphos)Ir(H)(eta3-MeC3H4)]BPh4 (5-anti), and [(triphos)Ir(H)(eta3-MeC3H4V-BPh4 (5-syn), and but-2-ene. At 100-degrees-C, the solid-gas reaction produces catalytic amounts of benzene, the real catalyst being the eta4-benzene complex 2. Comparison with fluid solution systems provides evidence for the control exerted by the constraining environment of the crystal lattice of the organometallic complex on the reaction.