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Rh(η5-2-ethyl-5-methyl-cyclopenta[b]thienyl)(CO)2 | 1021498-25-8

中文名称
——
中文别名
——
英文名称
Rh(η5-2-ethyl-5-methyl-cyclopenta[b]thienyl)(CO)2
英文别名
——
Rh(η5-2-ethyl-5-methyl-cyclopenta[b]thienyl)(CO)2化学式
CAS
1021498-25-8
化学式
C12H11O2RhS
mdl
——
分子量
322.19
InChiKey
UTGZVOWOMLSYSR-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

反应信息

  • 作为反应物:
    描述:
    Rh(η5-2-ethyl-5-methyl-cyclopenta[b]thienyl)(CO)2三苯基膦甲苯 为溶剂, 以100%的产率得到Rh(η5-2-ethyl-5-methyl-cyclopenta[b]thienyl)(CO)(PPh3)
    参考文献:
    名称:
    Evaluating the kinetic indenyl effect of a π-thiaphentalenyl ancillary ligand
    摘要:
    The magnitude of the "kinetic indenyl effect" for the pi-thiapentalenyl ligand, isoelectronic heteroanalogue of the indenyl ligand, has been tested using the reaction between complex, Rh(eta(5)-th)(CO)(2) 3 (th = 2-ethyl-5-methyl-cyclopenta[b]thienyl or thiapentalenyl) and PPh3 as a model process. Only moderate "kinetic indenyl effect" of the thiapentalenyl ligand was observed. The rational for such behavior was also supported by DFT computational correlation of ground and transition states for the reaction of carbonyl group substitution by a phosphine in the corresponding indenyl and thiapentalenyl rhodium complexes. (C) 2008 Published by Elsevier B.V.
    DOI:
    10.1016/j.jorganchem.2007.12.027
  • 作为产物:
    描述:
    di(rhodium)tetracarbonyl dichloride 、 一氧化碳 、 2-ethyl-5-methylcyclopenta[b]thienyl lithium 以 四氢呋喃 为溶剂, 以61%的产率得到Rh(η5-2-ethyl-5-methyl-cyclopenta[b]thienyl)(CO)2
    参考文献:
    名称:
    Evaluating the kinetic indenyl effect of a π-thiaphentalenyl ancillary ligand
    摘要:
    The magnitude of the "kinetic indenyl effect" for the pi-thiapentalenyl ligand, isoelectronic heteroanalogue of the indenyl ligand, has been tested using the reaction between complex, Rh(eta(5)-th)(CO)(2) 3 (th = 2-ethyl-5-methyl-cyclopenta[b]thienyl or thiapentalenyl) and PPh3 as a model process. Only moderate "kinetic indenyl effect" of the thiapentalenyl ligand was observed. The rational for such behavior was also supported by DFT computational correlation of ground and transition states for the reaction of carbonyl group substitution by a phosphine in the corresponding indenyl and thiapentalenyl rhodium complexes. (C) 2008 Published by Elsevier B.V.
    DOI:
    10.1016/j.jorganchem.2007.12.027
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