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[rhodium(I)(cycloocta-1,5-diene)(N(C6H5)CHC3H2N2(CH3))] tetrakis[3,5-bis(trifluoromethyl)phenyl]-borate | 1450619-16-5

中文名称
——
中文别名
——
英文名称
[rhodium(I)(cycloocta-1,5-diene)(N(C6H5)CHC3H2N2(CH3))] tetrakis[3,5-bis(trifluoromethyl)phenyl]-borate
英文别名
——
[rhodium(I)(cycloocta-1,5-diene)(N(C6H5)CHC3H2N2(CH3))] tetrakis[3,5-bis(trifluoromethyl)phenyl]-borate化学式
CAS
1450619-16-5
化学式
C19H23N3Rh*C32H12BF24
mdl
——
分子量
1259.54
InChiKey
BPQHYOCATWDIQS-JSHANCFJSA-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:
    描述:
    一氧化碳[rhodium(I)(cycloocta-1,5-diene)(N(C6H5)CHC3H2N2(CH3))] tetrakis[3,5-bis(trifluoromethyl)phenyl]-borate二氯甲烷 为溶剂, 反应 0.25h, 以76%的产率得到[rhodium(I)(carbonyl)2(N(C6H5)CHC3H2N2(CH3))] tetrakis[3,5-bis(trifluoromethyl)phenyl]-borate
    参考文献:
    名称:
    Cooperative Catalysis: Large Rate Enhancements with Bimetallic Rhodium Complexes
    摘要:
    A large increase in reaction rate was observed for the catalyzed mono- and dihydroalkoxylation of alkynes when structurally constrained bimetallic Rh(I) catalysts with imidazolyl-imine ligands were compared to their monometallic analogues. The "cooperative" enhancement was vastly improved by restricting the conformational freedom of the bimetallic structure and minimizing the intermetallic Rh center dot center dot center dot Rh distance.
    DOI:
    10.1021/om400613b
  • 作为产物:
    描述:
    [Rh(cod)2]BARF1-(1-methylimidazol-2-yl)-N-phenylmethanimine四氢呋喃 为溶剂, 反应 2.0h, 以89%的产率得到[rhodium(I)(cycloocta-1,5-diene)(N(C6H5)CHC3H2N2(CH3))] tetrakis[3,5-bis(trifluoromethyl)phenyl]-borate
    参考文献:
    名称:
    Cooperative Catalysis: Large Rate Enhancements with Bimetallic Rhodium Complexes
    摘要:
    A large increase in reaction rate was observed for the catalyzed mono- and dihydroalkoxylation of alkynes when structurally constrained bimetallic Rh(I) catalysts with imidazolyl-imine ligands were compared to their monometallic analogues. The "cooperative" enhancement was vastly improved by restricting the conformational freedom of the bimetallic structure and minimizing the intermetallic Rh center dot center dot center dot Rh distance.
    DOI:
    10.1021/om400613b
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相关结构分类