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| 190390-99-9

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
190390-99-9
化学式
C13H14FeNO2P
mdl
——
分子量
303.08
InChiKey
KYPYWFMOGSPECP-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:
    描述:
    、 sodium tetrahydroborate 在 NiCl2*6H2O 作用下, 以 四氢呋喃甲醇 为溶剂, 以89%的产率得到
    参考文献:
    名称:
    A New Concept for Chelate Ligands with Planar Chirality
    摘要:
    The chiral donor substituted phosphaferrocene derivatives CpFe(3,4-Me-2-2-R-C4HP) 6 (R = CH2CH2NMe2), 7 (R = CH2NMe2), and 8 (R = CH2OPPh2) were synthesized as racemates starting from 2-formyl-3,4-dimethylphosphaferrocene. The P,N-ligand 6 reacted with [Cp*RuCl](4) in THF to give the six-ring chelate complex Cp*RuCl(6) (=10) which was characterized by single-crystal X-ray diffraction analysis. The complexation reaction was found to proceed diastereoselectively with respect to the newly created stereogenic center on the ruthenium atom. Under similar conditions, the reaction of ligand 7 with [Cp*RuCl](4) did not lead to chelate formation. Instead, two isomers of the bis-P-coordinated complex Cp*RuCl(7)(2) (=11) were observed by NMR spectroscopy. Reaction of the phosphinite ligand 8 with (PhCN)(2)PdCl2 in toluene produced the six-ring chelate complex cis-PdCl2(8) (=12). The crystal structure of 12 has been determined.
    DOI:
    10.1021/om970059n
  • 作为产物:
    描述:
    硝基甲烷(3,4-dimethylphosphaferrocen-2-yl)carbaldehyde甲醇 为溶剂, 以78%的产率得到
    参考文献:
    名称:
    A New Concept for Chelate Ligands with Planar Chirality
    摘要:
    The chiral donor substituted phosphaferrocene derivatives CpFe(3,4-Me-2-2-R-C4HP) 6 (R = CH2CH2NMe2), 7 (R = CH2NMe2), and 8 (R = CH2OPPh2) were synthesized as racemates starting from 2-formyl-3,4-dimethylphosphaferrocene. The P,N-ligand 6 reacted with [Cp*RuCl](4) in THF to give the six-ring chelate complex Cp*RuCl(6) (=10) which was characterized by single-crystal X-ray diffraction analysis. The complexation reaction was found to proceed diastereoselectively with respect to the newly created stereogenic center on the ruthenium atom. Under similar conditions, the reaction of ligand 7 with [Cp*RuCl](4) did not lead to chelate formation. Instead, two isomers of the bis-P-coordinated complex Cp*RuCl(7)(2) (=11) were observed by NMR spectroscopy. Reaction of the phosphinite ligand 8 with (PhCN)(2)PdCl2 in toluene produced the six-ring chelate complex cis-PdCl2(8) (=12). The crystal structure of 12 has been determined.
    DOI:
    10.1021/om970059n
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