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Rh2(O2CCH3)4(3-CH3C5H4N)2 | 55960-36-6

中文名称
——
中文别名
——
英文名称
Rh2(O2CCH3)4(3-CH3C5H4N)2
英文别名
——
Rh2(O2CCH3)4(3-CH3C5H4N)2化学式
CAS
55960-36-6
化学式
C20H26N2O8Rh2
mdl
——
分子量
628.246
InChiKey
UOWGDJMXTGYTTC-UHFFFAOYSA-J
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:
    dirhodium tetraacetate 、 3-甲基吡啶乙醇 为溶剂, 反应 168.0h, 以91%的产率得到Rh2(O2CCH3)4(3-CH3C5H4N)2
    参考文献:
    名称:
    Synthesis, crystal structures and catalytic activity of tetrakis(acetato)dirhodium(II) complexes with axial picoline ligands
    摘要:
    Three complexes were synthesized in high yields by reaction of Rh-2(O2CCH3)(4) with 2-picoline (1), 3-picoline (2) and 4-picoline (3), respectively, and characterized by elemental analysis, ESI+-MS, FT-IR and H-1 NMR along with single-crystal X-ray structural analysis. All picoline ligands coordinate to the axial sites of Rh-2(O2CCH3)(4) via the pyridine nitrogen atoms, and interestingly, the coordination of 2-picoline in 1 is assisted by two intramolecular C-H center dot center dot center dot O hydrogen bonds formed between the methyl of 2-picoline and the oxygen atoms of Rh2(O2CCH3)(4). Moreover, the intermolecular C-H center dot center dot center dot O interactions play the main role in the structural stacking of 1-3. Their catalytic activity was evaluated in the C-H insertion reactions for the preparation of 4-nitrobenzyl-(4R, 5R, 6S)-6-((R)-1-hydroxyethyl)-4-methyl-3,7-dioxo-1-azabicyclo [3.2.0] heptane-2-carboxylate, a key intermediate of Meropenem. The isolated yields for 1, 2 and 3 are 44%, 16% and 22%, respectively, significantly lower than the value of Rh2(O2CCH3) 4 (73%), indicating that the axial ligands have negative but different influence on the catalytic activity. The activities of 1-3 are related to the displacement rate of the axial ligands, and essentially related to the Rh-N bond lengths which strong affect the displacement rate. Therefore, it is possible to tune the catalytic activity of Rh-2(O2CCH3)(4) by changing its axial ligands. (C) 2015 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2015.05.017
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文献信息

  • Mal'kova, T. A.; Shafranskii, V. N., Zhurnal Obshchei Khimii, 1975, vol. 45, p. 618 - 621
    作者:Mal'kova, T. A.、Shafranskii, V. N.
    DOI:——
    日期:——
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Rh: SVol.B2, 1.1.2.2.1.7, page 22 - 23
    作者:
    DOI:——
    日期:——
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