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Ru(CO)(triisopropylphosphine)(SC6H4N(CH3)CH2CH2N(CH3)C6H4S) | 590361-80-1

中文名称
——
中文别名
——
英文名称
Ru(CO)(triisopropylphosphine)(SC6H4N(CH3)CH2CH2N(CH3)C6H4S)
英文别名
——
Ru(CO)(triisopropylphosphine)(SC6H4N(CH3)CH2CH2N(CH3)C6H4S)化学式
CAS
590361-80-1
化学式
C26H39N2OPRuS2
mdl
——
分子量
591.784
InChiKey
RWHOINZTRONNJT-UHFFFAOYSA-L
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

  • 作为产物:
    描述:
    一氧化碳 、 以 四氢呋喃 为溶剂, 以98%的产率得到Ru(CO)(triisopropylphosphine)(SC6H4N(CH3)CH2CH2N(CH3)C6H4S)
    参考文献:
    名称:
    Metal thiolate complexes binding molecular nitrogen under mild conditions: [μ-N2{Ru(PiPr3)(N2Me2S2)}2], the first dinuclear example
    摘要:
    Binding N-2 to the metal sulfur cofactors of nitrogenase is considered the first step of biological N-2 fixation. In quest of low-molecular weight complexes modeling this step [mu-N-2{Ru((PPr3)-Pr-i)(N2Me2S2)}(2)] (3) was synthesized and completely characterized. Complex 3 was obtained from [Ru(N-2)((PPr3)-Pr-i)(N2Me2S2)] (1) that dissociates N-2 under reduced partial pressure of N,. Complex 1, in turn, forms from [Ru(CH3CN)((PPr3)-Pr-i)(N2Me2S2)] (2) and N-2 at standard conditions (20 degreesC, 1 bar) such that the formation of 3 corresponds with a binding of molecular nitrogen to metal thiolate complex fragments under mild conditions, not requiring abiologically strong reductants. Complex 3 forms as racemate of (R,R)-3 and (S,S)-3 enantiomers which spontaneously separate upon crystallization and could both be characterized by X-ray crystallography. Complex 3 exhibits short bonds trans to the N-2 ligand, a v(N-2) frequency (2042 cm(-1)) low in comparison with that of 1 (2113 cm(-1)) and a non-linear [Ru-NdropN-Ru] entity. The thiolate donors of 3 represent Broensted-basic sites for reversible protonations so that 3 becomes a complex suited for investigations aiming at the reduction of N-2 by nitrogenase-like coupled [2H(+)/2e(-)] transfer steps. (C) 2003 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(03)00008-2
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