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K[HRe(CO)4-(μ-H)-ReH(CO4)] | 1221273-60-4

中文名称
——
中文别名
——
英文名称
K[HRe(CO)4-(μ-H)-ReH(CO4)]
英文别名
——
K[HRe(CO)4-(μ-H)-ReH(CO4)]化学式
CAS
1221273-60-4
化学式
C8H3O8Re2*K
mdl
——
分子量
638.619
InChiKey
XAKMEHWVTLAPHQ-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

  • 作为产物:
    描述:
    Re2(μ-H)2(CO)8 、 potassium tri-sec-butyl-borohydride 以 tetrahydrofuran-d8 为溶剂, 生成 K[HRe(CO)4-(μ-H)-ReH(CO4)]
    参考文献:
    名称:
    New chain clusters of rhenium connected by Re–H–Re interactions: A low-temperature NMR investigation
    摘要:
    Low temperature NMR spectroscopy has been used to characterize the mixtures formed in the oligomerization reactions of the unsaturated complex [Re-2(mu-H)(2)(CO)(8)] (1), promoted by hydrido-carbonyl rhenates. Three families of chain clusters, constituted by Re(CO)(4) units connected through Re(mu-H)Re interactions, have been obtained. The first one, of general formula [(CO)(5)Re-{HRe(CO)(4)}(2n+1)], was formed using [HRe2(CO)(9)] as promoter. The nature of the products was confirmed by C-13 NMR of (CO)-C-13 enriched samples. The formation of Re-6 and Re-8 chain clusters was recognized. The other two families have general formula [H-{HRe(CO)(4)}(2n)] and [H-{HRe(CO)(4)}(2n+1)] and were obtained using as initiators [HB(Bu-s)(3)] or [H2Re(CO)(4)], respectively. Mixtures of oligomers with mean chain lengths higher than 10 have been observed. The addition of a strong acid caused H-2 evolution, leading back to the "monomer" 1. For all the three families, each oligomerization step was reversible, with the longer oligomers favoured at the lowest temperatures, where, however, the reactions were very slow, usually preventing the attainment of the equilibrium. Variable temperature NMR spectra revealed a dynamic process involving the terminal H2Re(CO)(4) moiety(ies), that simultaneously exchanges terminal/bridging hydrides and the carbonyls trans to them (Delta G(#) 41-44 kJ mol (1)). At room temperature, the more hydrogen-rich chain clusters also underwent dehydrogenation/cyclization reactions. (C) 2009 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2009.05.005
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