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{(μ-nitrido)bis(triphenylphosphorus)}{Rh(CO)2Cl2} | 89654-69-3

中文名称
——
中文别名
——
英文名称
{(μ-nitrido)bis(triphenylphosphorus)}{Rh(CO)2Cl2}
英文别名
cis-bis(triphenylphosphine)iminium dichlorodicarbonylrhodium(I)
{(μ-nitrido)bis(triphenylphosphorus)}{Rh(CO)2Cl2}化学式
CAS
89654-69-3
化学式
C2Cl2O2Rh*C36H30NP2
mdl
——
分子量
768.421
InChiKey
JTVQNMPBVCUICE-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

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

点击查看最新优质反应信息

文献信息

  • Promotion of the [PPN][Rh(CO)4]-catalysed carbonylation of nitrobenzene by 2-hydroxypyridine and related molecules: an apparent bifunctional activation
    作者:Fabio Ragaini、Emma Gallo、Sergio Cenini
    DOI:10.1016/s0022-328x(99)00502-1
    日期:2000.1
    2-Hydroxypyridine and related molecules have a large activating effect on the previously reported [PPN][Rh(CO)4]-based catalytic system for the reductive carbonylation of nitrobenzene to methyl phenylcarbamate (PPN+=(PPh3)2N+). The effect is not due to the known 2-hydroxypyridine–2-pyridone tautomeric equilibrium, since 4-hydroxypyridine, for which the same tautomeric equilibrium exists, completely
    2-羟基吡啶和相关分子对先前报道的基于[PPN] [Rh(CO)4 ]的催化体系具有很大的活化作用,该体系可将硝基苯还原羰基化为苯基氨基甲酸甲酯(PPN + =(PPh 3)2 N +) 。该作用不是由于已知的2-羟基吡啶-2-吡啶酮互变异构平衡所致,因为存在相同互变异构平衡的4-羟基吡啶完全抑制了反应。在先前分离的属环配合物[PPN] [,据信是催化反应的中间体。然而,催化反应速率对苯胺浓度的依赖性表明,发现的化学计量反应的影响不可能是与催化反应的加速有关的影响。因此,存在两种不同的作用,这两种作用似乎都归因于启动子分子中碱性位点和酸性位点的近端位置。
  • Hydroformylation of formaldehyde to give glycolaldehyde with halide-promoted Rh4(CO)12
    作者:Mario Marchionna、Giuliano Longoni
    DOI:10.1039/c39870001097
    日期:——
    Hydroformylation of paraformaldehyde and 37% aqueous formaldehyde to give glycolaldehyde with selectivity up to ca. 90% has been carried out in acetone at 90–140 °C and 100–140 atm of carbon monoxide–hydrogen with halide-promoted Rh4(CO)12 as catalyst precursor.
    聚甲醛和37%的甲醛溶液的加氢甲酰化反应生成的乙醇醛选择性高达约。90%已在丙酮中于90–140°C和100–140 atm的一氧化碳-氢气中进行了卤化促进的Rh 4(CO)12作为催化剂前体。
  • A spectroscopic study of halocarbonyl complexes of rhodium(I) and (III)
    作者:Brian T. Heaton、Chacko Jacob、Steven Moffet
    DOI:10.1016/0022-328x(93)83376-7
    日期:1993.12
    NMR studies (13C and 103Rh) show that mixing of equimolar amounts of [RhX2(CO)2]− and [RhY2(CO)2]− (X≠Y  Cl, Br, or I) results in approximately statistical X/Y exchange to give cis-[RhXY(CO)2]−. Products resulting from the addition of X2 to [RhX2(CO)2]− (X  Cl, Br, or I) have been characterized by NMR and IR spectroscopic studies, and include the anions cis- and trans-[RhX4(CO)2]− which slowly lose
    NMR研究(13 C和103 Rh)表明,等摩尔量的[RhX 2(CO)2 ] -和[RhY 2(CO)2 ] -(X≠YCl,Br或I)混合统计X / Y交换得到顺式-[RhXY(CO)2 ] -。将X 2加到[RhX 2(CO)2 ] -(X Cl,Br或I)中所得的产物已通过NMR和IR光谱学表征,包括阴离子cis-和反式-[RhX 4(CO)2 ] -缓慢失去CO,得到双(卤素)桥联的二聚体[Rh 2 X 8(CO)2 ] 2-;二聚体逐渐与卤化物反应,生成单(卤素)桥联的二聚体[Rh 2 X 9(CO)2 ] 3-,然后形成[RhX 5(CO)] 2-。甲醇将卤化物反式转化为CO的趋势按XCl
  • Convenient Synthesis and Molecular Structure of PPN[RhCl<sub>2</sub>(CO)<sub>2</sub>] (PPN<sup>+</sup> = Bis(triphenylphosphane)iminium)
    作者:Hans-Christian Böttcher、Peter Mayer
    DOI:10.5560/znb.2014-3325
    日期:2014.3.1
    complex anion cis-[RhCl2(CO)2]-. This species was formed in good yield and was characterized as its PPN salt (PPN+ = bis(triphenylphosphane)iminium cation). The molecular structure of the title compound PPN[RhCl2(CO)2] was confirmed by X-ray diffraction and shown to be isomorphous to PPN[IrCl2(CO)2] Graphical Abstract Convenient Synthesis and Molecular Structure of PPN[RhCl2(CO)2] (PPN+ = Bis(triphenylphosphane)iminium)
    - 的合三甲酸在回流的乙氧基乙醇,得到以方便的方式的公知的羰基chlorido络合物阴离子顺式 - [RhCl2(CO)2]反应。形成以良好的收率这种物种和被表征为它的盐PPN(PPN + =双(三苯基膦)亚阳离子)。标题化合物的PPN [RhCl2(CO)2]分子结构通过X射线衍射确认,并且显示出是同晶PPN [IrCl2(CO)2]图形摘要简便合成和PPN [RhCl2(CO)的分子结构2](PPN + =双(三苯基膦)亚
  • Galli, Daniele; Garlaschelli, Luigi; Ciani, Gianfranco, Journal of the Chemical Society, Dalton Transactions, 1984, p. 55 - 62
    作者:Galli, Daniele、Garlaschelli, Luigi、Ciani, Gianfranco、Fumagalli, Alessandro、Martinengo, Secondo、Sironi, Angelo
    DOI:——
    日期:——
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