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Re2(CO)7(PMe3)3(μ-SC6H4CHCH) | 268217-85-2

中文名称
——
中文别名
——
英文名称
Re2(CO)7(PMe3)3(μ-SC6H4CHCH)
英文别名
——
Re2(CO)7(PMe3)3(μ-SC6H4CHCH)化学式
CAS
268217-85-2
化学式
C24H33O7P3Re2S
mdl
——
分子量
930.923
InChiKey
TYGBOKLNLQWDPU-UHFFFAOYSA-M
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:
    Re2(CO)7(μ-SC6H4CHCH) 、 三甲基膦甲苯 为溶剂, 生成 Re2(CO)7(PMe3)2(μ-SC6H4CHCH) 、 Re2(CO)7(PMe3)3(μ-SC6H4CHCH)
    参考文献:
    名称:
    Organometallic models of catalytic hydrodesulfurization: Re2(CO)10-promoted cleavage of C–S bonds in benzothiophene
    摘要:
    含有 Re2(CO)10 和苯并噻吩(BT)的己烷溶液经紫外线光解后得到 CâS 裂解产物 Re2(CO)7[Î-2(C2,C3)-μ2(C 2,S)-BT] 1,该产物在室温下与 PMe3 反应生成两种膦取代产物 2 和 3,其中破碎的 BT 配体部分脱离了金属;1、2 和 3 的分子结构是催化剂表面 BT 加氢脱硫过程中可能出现的中间产物的模型。
    DOI:
    10.1039/a909161k
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文献信息

  • Re<sub>2</sub>(CO)<sub>10</sub>-Promoted S-Binding, C−S Bond Cleavage, and Hydrogenation of Benzothiophenes:  Organometallic Models for the Hydrodesulfurization of Thiophenes
    作者:Michael A. Reynolds、Ilia A. Guzei、Robert J. Angelici
    DOI:10.1021/ja011725l
    日期:2002.2.1
    In hydrodesulfurization model reactions of dinuclear metal complexes with thiophenes, we observe that ultraviolet photolysis of Re-2(CO)(10) and benzothiophenes (BT*) in hexanes solution produces the ring-opened BT* complexes Re-2(CO)(7) (mu-BT*) (1a-d) (BT* = benzothiophene (BT) 1a, 2-methylbenzothiophene (2-MeBT) 1b, 3-methylbenzothiophene (3-MeBT) 1c, and 3,5-dimethylbenzothiophene (3,5-Me2BT) 1d). The eta(1)(S)-bound BT* complexes Re-2(CO)(9)(eta(1)(S)-BT*) (2a-d), prepared from Re-2(CO)(9)(THF) and BT*, are readily converted into 1a-d in good yields (40-60%) during UV photolysis in hexanes solution, which suggests that the eta(1)(S)-bound complexes 2a-d are precursors to 1a-d in the reactions of Re-2(CO)(10) with BT*. Irradiation of Re-2(CO)(10) and 3,5-Me2BT with UV light in decane solution under an atmosphere of H-2 produces complex 1d and the partially hydrogenated BT* complex Re-2(CO())7(mu-3,5-Me2BT-H)(mu-H) (3d). Reactions of 1a with phosphines yield further ring-opened BT-Re complexes of the types Re-2(CO)(7)(PMe3)(3)-(mu-BT) (4) and Re-2(CO)(7)(PR3)(2) (mu-BT) (R = Me (5), Pr-i (6), Cy (7), and bis(diethylphosphino)ethane (8)). Structures of 1d, 2c, 3d, and 6, which demonstrate various bonding modes of benzothiophene and its C-S cleaved derivatives to two metal centers, were determined by X-ray crystallographic studies.
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