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[Re(2,2'-bipyridine)(CO)3(P(OEt)3)](PF6) | 186969-29-9

中文名称
——
中文别名
——
英文名称
[Re(2,2'-bipyridine)(CO)3(P(OEt)3)](PF6)
英文别名
——
[Re(2,2'-bipyridine)(CO)3(P(OEt)3)](PF6)化学式
CAS
186969-29-9
化学式
C19H23N2O6PRe*F6P
mdl
——
分子量
737.546
InChiKey
UHMHYVAALVKQGQ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

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:
    参考文献:
    名称:
    Key Process of the Photocatalytic Reduction of CO2 Using [Re(4,4‘-X2-bipyridine)(CO)3PR3]+ (X = CH3, H, CF3; PR3 = Phosphorus Ligands):  Dark Reaction of the One-Electron-Reduced Complexes with CO2
    摘要:
    Reduction of CO2 to CO was efficiently photocatalyzed by [Re(4,4'-X(2)bpy)(CO)(3)PR3](+) (X = H, Me; PR3 = P(OEt)(3), P(O-i-Pr)(3)) in quantum yields of 0.16-0.20. Complexes with CF3 as X or trialkylphosphine as PR3 have much lower photocatalytic ability. One-electron-reduced species of the complexes, which were produced by the photoinduced electron-transfer reaction with triethanolamine, reacted with CO2 in the dark with rate constants of 3.5 x 10(-4)-1.9 x 10(-2) M-1 s(-1). The faster the rate of this process, the higher the quantum yield of CO formation. The calculated amount of CO formation, based on the assumption that the process gives CO quantitatively, was similar to the actually observed amount under various conditions. This is consistent with the thermal process being one of the rate-limiting steps in the photocatalyzed reduction of CO2 by the rhenium complexes.
    DOI:
    10.1021/om970608p
  • 作为产物:
    描述:
    亚磷酸三乙酯tricarbonyl(2,2'-bipyridine)chlororhenium(I) 、 ammonium hexafluorophosphate 在 silver trifluoromethanesulfonate 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 3.0h, 以87%的产率得到[Re(2,2'-bipyridine)(CO)3(P(OEt)3)](PF6)
    参考文献:
    名称:
    Re(二亚胺)(CO) 2 (L)Cl(L = 膦或亚磷酸酯)化合物的非光化学合成
    摘要:
    摘要 报道了一系列 Re(二亚胺)(CO)2(L)Cl(其中 L = P(OEt)3,PMe3)类型的化合物的合成和表征。非光化学配体取代 (non-PLS) 利用磷配体的转稳定作用来促进羰基取代。非 PLS 途径导致单一异构体产品的高产率 (> 60%),与类似 PLS 途径的低产率、混合异构体产品相比具有优势。羰基被膦/亚磷酸酯配体取代,将吸收进一步转移到可见光区域,而不会降低摩尔吸收率。所提出的合成为相关的光敏中性铼/锰羰基卤化物化合物提供了一种通用的简便配体取代途径。
    DOI:
    10.1016/j.inoche.2015.07.001
  • 作为试剂:
    参考文献:
    名称:
    Key Process of the Photocatalytic Reduction of CO2 Using [Re(4,4‘-X2-bipyridine)(CO)3PR3]+ (X = CH3, H, CF3; PR3 = Phosphorus Ligands):  Dark Reaction of the One-Electron-Reduced Complexes with CO2
    摘要:
    Reduction of CO2 to CO was efficiently photocatalyzed by [Re(4,4'-X(2)bpy)(CO)(3)PR3](+) (X = H, Me; PR3 = P(OEt)(3), P(O-i-Pr)(3)) in quantum yields of 0.16-0.20. Complexes with CF3 as X or trialkylphosphine as PR3 have much lower photocatalytic ability. One-electron-reduced species of the complexes, which were produced by the photoinduced electron-transfer reaction with triethanolamine, reacted with CO2 in the dark with rate constants of 3.5 x 10(-4)-1.9 x 10(-2) M-1 s(-1). The faster the rate of this process, the higher the quantum yield of CO formation. The calculated amount of CO formation, based on the assumption that the process gives CO quantitatively, was similar to the actually observed amount under various conditions. This is consistent with the thermal process being one of the rate-limiting steps in the photocatalyzed reduction of CO2 by the rhenium complexes.
    DOI:
    10.1021/om970608p
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