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3,3'-(butane-1,4-diyl)bis(6,8-di-tert-butyl-2,2-bis((triphenylsilyl)oxy)-2H-2l4-benzo[e][1,3,2]oxazaborinin-3-ium) | 241476-26-6

中文名称
——
中文别名
——
英文名称
3,3'-(butane-1,4-diyl)bis(6,8-di-tert-butyl-2,2-bis((triphenylsilyl)oxy)-2H-2l4-benzo[e][1,3,2]oxazaborinin-3-ium)
英文别名
——
3,3'-(butane-1,4-diyl)bis(6,8-di-tert-butyl-2,2-bis((triphenylsilyl)oxy)-2H-2l4-benzo[e][1,3,2]oxazaborinin-3-ium)化学式
CAS
241476-26-6
化学式
C106H110B2N2O6Si4
mdl
——
分子量
1642.01
InChiKey
OIEDLGUPHOQYOQ-UHFFFAOYSA-N
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:
    (N,N'-butylenebis(3,5-di-tert-butyl(2-O)benzylidenimine)[B(OCH3)2]2三苯基硅醇甲苯 为溶剂, 以62%的产率得到3,3'-(butane-1,4-diyl)bis(6,8-di-tert-butyl-2,2-bis((triphenylsilyl)oxy)-2H-2l4-benzo[e][1,3,2]oxazaborinin-3-ium)
    参考文献:
    名称:
    Synthesis and Structures of Salen-Supported Borates Containing Siloxides
    摘要:
    The ligand N,N"-bis(2-hydroxybenzylidene)diethylenetriamine (SalenN(3)H(3)) was used to prepare the compound SalenN(3)H{B(OMe2)}(2) (1) which could, in turn, be used in the formation of SalenN(3)H{B(OSiPh3)(2)}(2) (2). For comparative purposes, the compounds Salben{B(OSiPh3)(2)}(2) (3) (Salben = N,N'-butylenebis(2-hydroxybenzylideneamine), Salen(Bu-t){B(OSiPh3)(2)}(2) (4) (Salen(Bu-t) = N,N'-ethylenebis(3,5-di-tert-butyl-2-hydroxy-benzylideneamine) and Salben(Bu-t){B(OSiPh3)(2)}(2) (5) (Salben(Bu-t) = N,N'-butylenebis(3,5-di-tert-butyl-2-hydroxybenzylideneamine) were prepared. In reactions where the siloxide is (HO)(2)SiPh2, unique dimeric siloxide-bridged compounds result, [Salpten(Bu-t){B(O2SiPh2}](2) (6) and [SalenN(3)H{B(O2SiPh2)}](2) (7). Compound 6 possesses a zeolite-like cavity having a volume of 157 Angstrom(3). All Of the compounds were characterized by physical (mp, analyses) and spectroscopic techniques (H-1 and B-11 NMR, IR) and, in the case of 1, 3, 4, and 6, by X-ray crystallography.
    DOI:
    10.1021/ic9812003
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