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[RuHCl(bis(pyrazol-1-yl)methane)(cycloocta-1,5-diene)] | 152391-12-3

中文名称
——
中文别名
——
英文名称
[RuHCl(bis(pyrazol-1-yl)methane)(cycloocta-1,5-diene)]
英文别名
[RuHCl(1,5-cyclooctadiene)(bis(pyrazol-1-yl)methane)];[RuHCl(1,5-cyclooctadiene)](bis(pyrazol-1-yl)methane);chloro(hydrido)ruthenium;(1Z,5Z)-cycloocta-1,5-diene;1-(pyrazol-1-ylmethyl)pyrazole
[RuHCl(bis(pyrazol-1-yl)methane)(cycloocta-1,5-diene)]化学式
CAS
152391-12-3
化学式
C15H21ClN4Ru
mdl
——
分子量
393.882
InChiKey
YCBNTWSJQRJLSA-SUESZSCISA-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

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:
    [RuHCl(bis(pyrazol-1-yl)methane)(cycloocta-1,5-diene)]K(2-phenoxy-bis(pyrazol-1-yl)methane)四氢呋喃 为溶剂, 以50%的产率得到RuH(κ(3)-2-phenoxy-bis(pyrazol-1-yl)methane)(1,5-cyclooctadiene)
    参考文献:
    名称:
    氢化钌与衍生自甲烷的杂蝎子配体的配合物:2-苯氧基-双(吡唑-1-基)甲烷。配体在取代和质子转移反应中的半不稳定作用
    摘要:
    络合物[期RuH(κ 3 -bpzmPhO)(COD)](1)通过反应合成[期RuH(COD)(NH 2 NME 2)3 ] [BPH 4 ]与2-苯氧基-双钾盐(吡唑-1-基)甲烷(bpzmPhOK)。这种配位体采用κ 3 - Ñ,Ñ,Ò上的金属中心配位使人想起的通常trispyrazolylborate络合物中观察到的情况。络合物1以两种处于平衡状态的非对映异构体的混合物形式存在于溶液中。的反应1不同膦PME(3,PME 2 PH,PMePh2和PPh 3)已被研究。反应产物不仅取决于膦的性质,还取决于配合物:L的比率和温度。化学计量的二膦衍生物[期RuH(κ 1 - Ö -bpzmPhO)(鳕鱼)L- 2 ](L = PME 3,PME 2 PH)和[期RuH(κ 3 -bpzmPhO)L- 2 ](L = PME 3,PME 2制备了Ph,PMePh 2,PPh 3)。类似地,式[tetraphosphine衍生物顺-
    DOI:
    10.1016/j.poly.2003.11.023
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文献信息

  • Synthesis and spectroscopic studies of new hydridoruthenium complexes: catalytic reactions of [RuHCl(bpzm)(cod)] (bpzm = bis(pyrazol-1-yl)methane, cod = cycloocta-1,5-diene)
    作者:Félix A. Jalón、Antonio Otero、Ana Rodríguez、Mercedes Pérez-Manrique
    DOI:10.1016/0022-328x(95)05836-e
    日期:1996.2
    greatly depending on the reaction conditions. The complex trans-[RuHP(OMe)3}(bpzm)(cod)]CF3SOP3 (5a), which also readily isomerizes to cis[RuHP(OMe)3}(bpzm)(cod)]CF3SO3 (5b), was isolated from the reactions of 2 with P(OMe)3, or alternatively from the reaction of 1 with P(OMe)3 and AgCF3SO3. Finally, the reaction of 2 or 1 (in the presence of AgCF3SO3) with N-donors pyridine, 4-methylpyridine (4-picoline)
    [RuHCl(bpzm)(cod)](1)(bpzm =双(吡唑-1-基)甲烷,cod =环辛-1,5-二烯)与一当量的AgCF 3 SO 3反应,得到三氟甲磺酸酯-含有[RuH(CF 3 SO 3)(bpzm)(cod)](2)。2与PMe 2 Ph的反应允许合成反式-[RuH(PMe 2 Ph)(bpzm)(cod)] CF 3 SO 3(bd3a),该异构体易于异构化为顺式-[RuH(PMe 2 Ph)( bpzm)(cod)] CF 3 SO 3(3b),而类似的反应是1在AgCF 3 SO 3的存在下,生成了一系列含膦的配合物,例如[RuH(CF 3 SO 3)(cod)(PMe 2 Ph)2 ](4),该过程的产物在很大程度上取决于反应条件。复杂的反式-[RuH P(OMe)3 }(bpzm)(cod)] CF 3 SOP 3(5a),它也容易异构化为顺式[RuH P(OMe)3
  • Three-centre dihydrogen bond with fast interchange between proton and hydride: a very active catalyst for D+–H2 exchange†
    作者:A. Caballero、F. A. Jalón
    DOI:10.1039/a803972k
    日期:——
    Protonation of a ruthenium hydride containing the hemilabile ligand PPh2py gave a complex with a three-centre dihydrogen bond (Ru–H···H–Py2), and this system exhibits a fast proton/hydride interchange and is a very active catalyst for D+–H2 exchange.
    对含有半亲和配体 PPh2py 的氢化进行质子化处理后,得到了一种具有三中心二氢键(RuâHÂ-Â-Â-HâPy2)的配合物,该体系表现出快速的质子/氢化物交换,是一种非常活跃的 D+âH2 交换催化剂。
  • A study of the coordination ability of 2,5-di(2-pyridyl)phospholes on Ru centres
    作者:Agustı́n Caballero、Félix A Jalón、Blanca R Manzano、Mathieu Sauthier、Loı̈c Toupet、Régis Réau
    DOI:10.1016/s0022-328x(02)01803-x
    日期:2002.12
    The coordination behaviour of the readily available 1-phenyl-2,5-di(2-pyridyl)phosphole (NPN) toward Ru centres was investigated. Neutral and ionic compounds of formula [RuCl(p-cymene)(NPN)]TfO (TfO = CF3SO3)... (1), [RuCl(p -cyme-ne)(NPN)]BF4 (2), [RuCl(C6Me6)(NPN)]TfO (3), RuCp'Cl(NPN) [CP' = C5H5 (4), C5Me5 (5)], Ru(C5Me5)(sigma(1)-C8H13)(NPN) (6), RUCl2(NPN)(2) (7) and RuCIH(cod)(NPN) (cod = 1,5-cyclooctadiene) (8) were obtained. Two diastereomers were obtained for 1, 2 and 4, (a, b) while three were found in the case of 8 (a-c). According to NMR spectroscopy, the 2,5-bis(2-pyridyl)phosphole acts as a 1,4-P,N chelate ligand in all cases. This behaviour was confirmed by an X-ray diffraction study performed on complex 1a. Proton transfer studies on complex 8 demonstrated the influence of the molecular structure on the ability to form dihydrogen bridges. (C) 2002 Elsevier Science B.V. All rights reserved.
  • Jalon, Felix A.; Lopez-Agenjo, Ana; Manzano, Blanca R., Journal of the Chemical Society, Dalton Transactions
    作者:Jalon, Felix A.、Lopez-Agenjo, Ana、Manzano, Blanca R.、Moreno-Lara, Montserrat、Rodriguez, Ana、et al.
    DOI:——
    日期:——
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