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| 129434-13-5

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
129434-13-5
化学式
C40H35ClN2OP2Ru
mdl
——
分子量
758.201
InChiKey
ZQPLXLPTZQNRAX-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

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:
    (1,5-cyclooctadiene)(methoxy)iridium(I) dimer 、 丙酮 为溶剂, 以48%的产率得到
    参考文献:
    名称:
    异双核Ru-Ir和Ru-Rh配合物的合成和催化活性。[H(CO)(PPh 3)2 Ru(μ-Cl)(μ-pz)Ir(TFB)]的晶体结构(pz =吡唑酸盐,TFB =四氟苯并戊烯)
    摘要:
    钌化合物[RuHCl(CO)(PR 3)n ](R = Ph,n = 3; R = i Pr,n = 2)与吡唑C 3 H 4 N 2(Hpz)的反应生成络合物[RuHCl (CO)(Hpz)(PR 3)2 ]。用氢提取剂(甲醇离子或乙酰丙酮(acac))处理这些络合物,例如[M(μ-OMe)(二烯烃)] 2(M = Ir,Rh;二烯烃=环辛-1,5-二烯(COD) ),tetrafluorobenzobarrelene(TFB))或[钯(ACAC)(η 3 -C 3 H ^ 5)]赋予了异双核配合[H(CO)(PR 3)2 Ru(μ-Cl)(μ-pz)ML 2 ](R = Ph; M = Ir或Rh,L 2 = COD或TFB; R = i Pr,M = Rh,L 2 = TFB; R = Ph ,M = Pd,L 2= C 3 H 5)。通过X射线衍射研究确定了[H(CO)(PPh 3)2
    DOI:
    10.1016/0022-328x(90)85382-9
  • 作为产物:
    描述:
    吡唑 、 [RuHCl(CO)(PPh3)3] 以 乙醇 为溶剂, 以96%的产率得到
    参考文献:
    名称:
    异双核Ru-Ir和Ru-Rh配合物的合成和催化活性。[H(CO)(PPh 3)2 Ru(μ-Cl)(μ-pz)Ir(TFB)]的晶体结构(pz =吡唑酸盐,TFB =四氟苯并戊烯)
    摘要:
    钌化合物[RuHCl(CO)(PR 3)n ](R = Ph,n = 3; R = i Pr,n = 2)与吡唑C 3 H 4 N 2(Hpz)的反应生成络合物[RuHCl (CO)(Hpz)(PR 3)2 ]。用氢提取剂(甲醇离子或乙酰丙酮(acac))处理这些络合物,例如[M(μ-OMe)(二烯烃)] 2(M = Ir,Rh;二烯烃=环辛-1,5-二烯(COD) ),tetrafluorobenzobarrelene(TFB))或[钯(ACAC)(η 3 -C 3 H ^ 5)]赋予了异双核配合[H(CO)(PR 3)2 Ru(μ-Cl)(μ-pz)ML 2 ](R = Ph; M = Ir或Rh,L 2 = COD或TFB; R = i Pr,M = Rh,L 2 = TFB; R = Ph ,M = Pd,L 2= C 3 H 5)。通过X射线衍射研究确定了[H(CO)(PPh 3)2
    DOI:
    10.1016/0022-328x(90)85382-9
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文献信息

  • Synthesis of mononuclear complexes of Ru and Os and heterobimetallic M–M′(M = Ru or Os; M′= Rh, Ir, or Au) compounds with pyrazolate or imidazolate type ligands. X-Ray crystal structure of [(Ph<sub>3</sub>P)<sub>2</sub>(OC)HRu(µ-bim)Rh(cod)](bim = dianion of 2,2′-bi-imidazole, cod = cyclo-octa-1,5-diene)
    作者:María P. García、Ana M. López、Miguel A. Esteruelas、Fernando J. Lahoz、Luis A. Oro
    DOI:10.1039/dt9900003465
    日期:——
    The synthesis and characterization of several mono- and poly-(di-, tri-, or tetra)-nuclear compounds are reported. The mononuclear compounds are of the type [MH(CO)(HL)(PPh3)2][M = Ru or Os; [HL = Hbim (monoanion of 2,2′-bi-imidazole), Hbbzim (monoanion of 2,2′-bibenzi-imidazole)], or [RuH(pz)(CO)(Hpz)(PPh3)2][Hpz(pyrazole)]. They react with [M′(µ-OMe)(diolefin)}2]M′= Rh or Ir; diolefin = cyclo-octa-1
    报道了几种单-和多-(二,三或四)核化合物的合成和表征。单核化合物的类型为[MH(CO)(HL)(PPh 3)2 ] [M = Ru或Os; [HL = Hbim(2,2'-联咪唑单阴离子),Hbbzim(2,2'-联苯咪唑单阴离子)]或[RuH(pz)(CO)(Hpz)(PPh 3)2 ] [Hpz(吡唑)]。它们与[M'(µ-OMe)(二烯烃)} 2 ] [M'= Rh或Ir; 二烯烃=环-八-1,5-二烯(cod)或四氟苯戊烯四氟苯并-[5,6]双环[2.2.2]八-2,5,7-三烯)(tfbb)},得到异双核配合物[ (Ph 3 P)2(OC)HMLM'(二烯烃)]。在这些化合物中的某些化合物中,二烯烃可以很容易地被一氧化碳取代,从而产生[(Ph 3 P)2(OC)HRuL 2 M'(CO)2 ] [L 2 = bbzim,M'= Rh;L 2=(pz)2,M'= Rh或Ir]。[(Ph
  • Indirect cooperative effects leading to synergism in bimetallic homogeneous catalysts containing azolates as bridging ligands
    作者:Miguel A. Esteruelas、Maria P. Garcia、Ana M. Lopez、Luis A. Oro
    DOI:10.1021/om00047a039
    日期:1991.1
    The binuclear compounds [H(CO)(PPh3)2Ru(mu-bim)Ir(COD)] (1) (bim = 2,2'-biimidazolate, COD = 1,5-cyclooctadiene) and [H(CO)(PPh3)2Ru(mu-pz)2Ir(TFB)] (2) (pz = pyrazolate, TFB = tetrafluorobenzobarrelene) are more active catalysts for the hydrogenation of cyclohexene than the mononuclear parent compounds [RuH(Hbim)(CO)(PPh3)2], [Ir(Hbim)(COD)], [RuH(pz)(CO)(Hpz)(PPh3)2], and [Ir(TFB)-(Hpz)2]BF4. In the presence of 1, the reaction rate is first order with respect to the concentration of 1 and cyclohexene, second order with respect to hydrogen pressure, and inversely proportional to the concentration of added phosphine. For the reaction catalyzed by 2, the experimental data are in accordance with a rate expression of the form -d[cyclohexene]/dt = k[2][cyclohexene]P(H2) [P(H2) = hydrogen pressure]. On the basis of the kinetic results and experimental evidence, the origin of the catalytic synergism is assigned to indirect cooperative effects between the metallic centers of the binuclear complexes. The kinetic investigation of the hydrogenation of cyclohexene catalyzed by [Ir(mu-pz)(TFB)]2 (3) is also reported, suggesting that the full catalytic cycle involves binuclear species.
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