(CO)Fe(5,10,15-tris(2,6-dichlorophenyl)corrole)(1-) | 431892-37-4

• 英文名称: (CO)Fe(5,10,15-tris(2,6-dichlorophenyl)corrole)(1-)
• CAS: 431892-37-4
• 化学式: C₃₈H₁₇Cl₆FeN₄O
• 分子量: 814.144
• InChiKey: LJZRPCOHOYIVOZ-UNFHWNMOSA-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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• 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：

  Fe(5,10,15-tris(2,6-dichlorophenyl)corrole) 、 一氧化碳 在 对三联苯 、 三乙胺 作用下， 以 乙腈 为溶剂， 生成 (CO)Fe(5,10,15-tris(2,6-dichlorophenyl)corrole)(1-)
  参考文献：
  名称：

  Reduction of Cobalt and Iron Corroles and Catalyzed Reduction of CO₂

  摘要：

  The role of cobalt and iron corroles in catalytic CO2 reduction has been studied. Chemical, electrochemical, and photochemical reductions of the stable metal corroles Ph3PCoIII(tpfc) (tpfc = 5,10,15-tris(pentafluorophenyl)corrole), ClFeIV(tpfc), and CIFeIV(tdcc) (tdcc = 5,10,15-tris(2,6-dichlorophenyl)corrole) have been carried out in acetonitrile solutions. Stepwise reduction to the [M-II(tpfc)](-) and [M-1(tpfc)](2-) states was observed in all cases. Gradual reduction with sodium amalgam permitted recording of the optical absorption spectra of the various oxidation states and showed that the M-1 state reacts with CO2. Cyclic voltammetry in Ar-saturated acetonitrile solutions permitted determination of the following half-wave potentials: for Ph3PCOIII (tpfc), 1.11 V, 0.72 V, -0.42 V (E-pc), - 1.44 V, -2.3 V (E-pc); for ClFeIV(tpfc), 0.44 V, - 1.01 V (E-pc), - 1.60 V, -2.2 V (E-pc); for ClFeIV(tdcc), 0.24 V, - 1.18 V (E-pc), - 1.78 V vs SCE with a scan rate of 0. 1 V s(-1). Cyclic voltammetry in CO2-saturated solutions indicated that the Co-1 and Fe-1 complexes react with CO2 and that the reduced Fe(tdcc) complex is the most efficient electrocatalyst for CO2 reduction, showing the largest catalytic currents among these corroles. Photochemical reduction in CO2-saturated acetonitrile solutions containing p-terphenyl (TP) as a sensitizer and triethylamine (TEA) as a reductant led to production of CO and H, These experiments also show that Fe(tdcc) is more effective than the other corroles as a CO2 reduction catalyst. The present finding that the M-1 oxidation states of the cobalt and iron corroles can react with CO2 is in contrast with the case of the respective porphyrins and phthalocyanines, which do not react with CO2 until they are reduced beyond the M-1 state.

  DOI：

  10.1021/jp013668o