{(triphos)IrCl(C2H4)} | 128549-59-7

• 英文名称: {(triphos)IrCl(C2H4)}
• CAS: 128549-59-7
• 化学式: C₄₃H₄₃ClIrP₃
• 分子量: 880.409
• InChiKey: LVSRWCFRIFYYJC-UHFFFAOYSA-M

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

• 作为反应物：
  描述：

  {(triphos)IrCl(C2H4)} 在 氧气 作用下， 以 二氯甲烷 为溶剂， 以95%的产率得到{(triphos)IrCl(η2-O2)}
  参考文献：
  名称：

  Oxidation of primary alcohols to carboxylic acids made easy at iridium

  摘要：

  DOI：

  10.1021/ja00174a051
• 作为产物：
  描述：

  diμ-chlorotetrakis(η2-cyclooctene)diiridium(I) 、 1,1,1-三(二苯基膦甲基)乙烷 在 ethylene 作用下， 以 四氢呋喃 为溶剂， 以85%的产率得到{(triphos)IrCl(C2H4)}
  参考文献：
  名称：

  Barbara, Pierluigi; Bianchini, Claudio; Meli, Andrea, Organometallics, 1991, vol. 10, # 7, p. 2227 - 2238

  摘要：

  DOI：

文献信息

• Dioxygen uptake and transfer by Co(III), Rh(III) and Ir(III) catecholate complexes
  作者：Pierluigi Barbaro、Claudio Bianchini、Klaus Linn、Carlo Mealli、Andrea Meli、Francesco Vizza、Franco Laschi、Piero Zanello

  DOI：10.1016/s0020-1693(00)92345-4

  日期：1992.8

  compounds undergo electron-transfer reactions that encompass the M(III), M(II) and M(I) oxidation states of the metal, and the catecholate, semiquinone and quinone oxidation levels of the quinoid ligand. Paramagnetic Ir(III) semiquinonate complexes, [(triphos)Ir(SQ)]2+, and Ir(II) catecholates, [(triphos)Ir(Cat)], have been characterized by X-band ESR spectroscopy. The reactions of the metal catecholates in

  摘要已合成了大量通式为[（triphos）M（Cat）] Y的五配位金属儿茶酚盐配合物，并通过化学，光谱和电化学技术对其进行了表征（MCo，Rh，Ir； Cat = 9， 10-邻苯二酚邻苯二甲酸酯，1,2-萘邻苯二甲酸酯，3,5-二叔丁基邻苯二甲酸酯，4-甲基邻苯二甲酸酯，4-羧基邻苯二甲酸酯-乙酯，四氯邻苯二甲酸酯; Y = BPh4，PF6; triphos = MeC（CH2PPh2）3）。所有这些化合物都经历电子转移反应，其中包括金属的M（III），M（II）和M（I）氧化态，以及醌型配体的儿茶酸，半醌和醌氧化水平。顺磁性的Ir（III）半奎宁酸盐络合物[（triphos）Ir（SQ）] 2+和Ir（II）儿茶酚酸盐[（triphos）Ir（Cat）]已通过X波段ESR光谱进行了表征。已经研究了非水介质中儿茶酚酸金属与双氧的反应。除极少数例外外，所有化合物均与O2反应生成通式[（triphos）M（OO）（SQ）]
• Barbaro, Pierluigi; Bianchini, Claudio; Frediani, Piero, Inorganic Chemistry, 1992, vol. 31, # 8, p. 1523 - 1529
  作者：Barbaro, Pierluigi、Bianchini, Claudio、Frediani, Piero、Meli, Andrea、Vizza, Francesco

  DOI：——

  日期：——
• Bianchini, Claudio; Caulton, Kenneth G.; Chardon, Catherine, Journal of the American Chemical Society, 1991, vol. 113, # 13, p. 5127 - 5129
  作者：Bianchini, Claudio、Caulton, Kenneth G.、Chardon, Catherine、Eisenstein, Odile、Folting, Kirsten、Johnson, Todd J.、Meli, Andrea、Peruzzini, Maurizio、Rauscher, David J.、Streib, William E.、Vizza, Francesco

  DOI：——

  日期：——
• The Mechanism of Acetylene Cyclotrimerization Catalyzed by the fac-IrP3+ Fragment: The Relationship between Fluxionality and Catalysis
  作者：Claudio Bianchini、Kenneth G. Caulton、Catherine Chardon、Marie-Liesse Doublet、Odile Eisenstein、Sarah A. Jackson、Todd J. Johnson、Andrea Meli、Maurizio Peruzzini

  DOI：10.1021/om00017a067

  日期：1994.5

  Reaction of [(triphos)Ir(C2H4)2](BPh4) with C2H2 at 25-degrees-C gives [(triphos)Ir(eta4-C6H6)](BPh4), 1, which was shown to have this Ir/benzene connectivity by single crystal X-ray diffraction. Crystal data (-155-degrees-C): a = 16.471(6) angstrom, b = 17.126(6) angstrom, c = 12.030(4) angstrom, alpha = 101.22(2)-degrees, beta = 93.61(2)-degrees, and gamma = 75.46(1)-degrees with Z = 2 in space group Pi. This species reacts with C2H2 in the presence of Cl- to give (triphos)IrCl(eta2-C4H4), 2, which can be converted back to 1 with C2H2 in the presence of the chloride scavenger TlPF6. Ethyne will displace C6H6 from 1 at 60-degrees-C in THF, thus completing a catalytic cyclotrimerization of C2H2 to benzene. While the phosphorus nuclei in 1 form an AM2 spin system, these undergo site exchange with activation parameters DELTAH = 10.7(3) kcal/mol and DELTAS = -9.5(6) kcal-1 mol-1. The benzene ring H-1 NMR spectra are also temperature-dependent, and the fluxionality can be accounted for by the same activation parameters appropriate to P-31 site exchange; the same physical mechanism thus accomplishes both site exchanges. The structural study indicates that eta4-C6H6, which is nonplanar, is a stronger pi-acceptor than is butadiene itself. A multistep mechanism has been studied with extended Huckel calculations. It is shown that the C-C bond formation between the first two alkynes to give the unsaturated metallacyclopentadiene is permitted when the three spectator ligands are in a fac geometry but is forbidden when they are in a mer geometry, which explains the puzzling difference of reactivity between monodentate triphosphine and tripodal complexes. It is shown that this unsaturated metallacycle is highly reactive toward an incoming ligand since it is not strongly stabilized by conjugation within the pi system. This explains why it can be isolated by trapping with a Lewis base. The addition of the third alkyne to the metallacyclopentadiene, leading to the eta4-benzene complex, can be achieved in a concerted manner and leads directly to the product. The C-C bond lengths within the eta4-benzene are shown to be due to the presence of a potent metal donor and to the nonplanarity of the benzene ring. The fluxionality of the eta4-benzene, which makes all carbons of the ring and the three phosphine ligands equivalent on the NMR time scale, is suggested to be due to an easy displacement/rotation of the IrP3+ fragment around the ring. This displacement avoids eta6-coordination (20-electron species) but passes through unsaturated eta3- and eta2-benzene coordination modes. These unsaturated species (notably the eta2 one) have the proper low-lying LUMO to coordinate an additional alkyne. This leads back to the monoalkyne complex and benzene production. Fluxionality and reactivity of the eta4-benzene ring are therefore interrelated. The efficiency of the catalysis is suggested to be due to the fact that all intermediates are reactive 16-electron species stabilized by additional donation from the conjugated pi system of the organic ligand. The presence of an enforced fac arrangement of the three spectator ligands avoids the thermodynamic trap of the trigonal bipyramidal bis(alkyne) complex.