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| 1450924-86-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1450924-86-3
化学式
C49H55FeN2O2Sb
mdl
——
分子量
881.585
InChiKey
GXCPSHOWRBIIDT-WVABMSMOSA-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

  • 作为产物:
    描述:
    二茂铁甲酸 、 [o-C6H4(CHNC6H3iPr2-2,6)]Sb[o-C6H4CH2N(C6H3iPr2-2,6)] 以 正己烷 为溶剂, 反应 1.0h, 以82%的产率得到
    参考文献:
    名称:
    Opening of the azastibol heterocycle with various acids: Isolation of novel N,C-chelated organoantimony(III) compounds
    摘要:
    The reaction of N,C-intramolecularly coordinated organoantimony(III) compound L2SbCl (1) (where L is [2-(2',6'-i-Pr2C6H3)N=CHC6H4]) with one molar equivalent of the K-selectride (K[B(s-Bu)(3)H]) gave compound LSb{2-[CH2N(2',6'-i-Pr2C6H3)]C6H4} (2) containing five membered aza-stiba heterocycle. On the contrary, analogical reaction between the organobismuth(III) compound L2BiCl (3) and K-selectride gave only inseparable mixture of products. Reactions of 2 with selected acids HX resulted in the cleavage of the present Sb-N bond and formation of novel N, C-chelated compounds LSb(X){2-[CH2NH(2',6'-i-Pr2C6H3)]C6H4} (where X = Cl (4), CH3COO (5), CF3COO (6), CF3SO3 (7) or FcCOO (8); Fc = ferrocenyl). Compounds 4-8 were characterized by the help of elemental analysis, electrospray ionization (ESI) mass spectrometry, multinuclear NMR spectroscopy, IR spectroscopy and in the case of 5 by the single-crystal X-ray diffraction analysis. The molecular structures of compounds LSb(X){2-[CH2NH(2',6'-i-Pr2C6H3)]C6H4}center dot HX (where X = CF3COO (6a), CF3SO3 (7a)) were determined by the single-crystal X-ray diffraction analysis as well. Compounds 6a and 7a are most probably products of partial hydrolysis of compounds 6 and 7. (C) 2013 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2013.06.023
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