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mer-[RhCl3(2,6-C5H3N(CMe2NH2)2)] | 935658-64-3

中文名称
——
中文别名
——
英文名称
mer-[RhCl3(2,6-C5H3N(CMe2NH2)2)]
英文别名
mer-[RhCl3(2,6-bis(α-aminoisopropyl)pyridine)]
mer-[RhCl3(2,6-C5H3N(CMe2NH2)2)]化学式
CAS
935658-64-3
化学式
C11H19Cl3N3Rh
mdl
——
分子量
402.556
InChiKey
ZFWOCWSESSHZJB-UHFFFAOYSA-K
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

  • 作为产物:
    描述:
    氯化铑(三水)2,6-bis(α-aminoisopropyl)pyridine乙醇 为溶剂, 以96%的产率得到mer-[RhCl3(2,6-C5H3N(CMe2NH2)2)]
    参考文献:
    名称:
    Synthesis and exploratory coordination chemistry of the new ditertiary carbinamine ligand 2,6-bis(α-aminoisopropyl)pyridine
    摘要:
    The new pyridine-based N boolean AND N boolean AND N tridentate ligand 2,6-C5H3N(CMe2NH2)(2) (1) was synthesized by the treatment of 2,6-pyridinedicarbonitrile with an excess of the organocerium reagent in situ generated from CeCl3 and methyllithium in THF. The reaction of 1 with [RuCl2(PPh3)(3)] in THF at ambient conditions afforded (OC-6-23)-[RuCl{2,6-C5H3N(CMeNH2)(2)}(PPh3)(2)]Cl (2). The corresponding dimethyl sulfoxide complex [RuCl{2,6-C5H3N(CMe2NH2)(2)} {S(O)Me-2}(2)]Cl (3) was isolated as a mixture of the (OC-6-23) and (OC-632) stercoisonters 3a and 3b from the reaction between 1 and (OC-6-22)-[RuCl2 {S(O)Me-2}(3)(OSMe2)] in toluene at 80 degrees C. A prolonged interaction in toluene at reflux temperature gave isomerically pure 3a. The metal trichloride hydrates MCl3 - xH(2)O (M = Ru, Rh, Ir; x congruent to 2-4) produced mer-[RuCl3{2,6-C5H3N(CMe2NH2)(2)}] (M = Ru: 4; Rh: 5; Ir: 6), when combined with I in refluxing ethanol. The crystal structures of the following compounds were determined: ligand 1 and complexes 2 5 as addition compounds 2 - CH2Cl2, 3a (.) C7H8, ;4 (.) EtOH and 5 (.) 2(1)/2DMF. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2006.08.025
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