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([Me2Si(μ-N(tert-butyl))2PO(N(SiMe3)Ph)]VCl3(THF)) | 1056896-89-9

中文名称
——
中文别名
——
英文名称
([Me2Si(μ-N(tert-butyl))2PO(N(SiMe3)Ph)]VCl3(THF))
英文别名
——
([Me2Si(μ-N(tert-butyl))2PO(N(SiMe3)Ph)]VCl3(THF))化学式
CAS
1056896-89-9
化学式
C23H46Cl3N3O2PSi2V
mdl
——
分子量
641.082
InChiKey
FYYZKACOTDQDCT-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:
    [VCl3(thf)3][Me2Si(μ-N(tert-butyl)2)PO(N(SiMe3)Ph)]甲苯 为溶剂, 以59%的产率得到([Me2Si(μ-N(tert-butyl))2PO(N(SiMe3)Ph)]VCl3(THF))
    参考文献:
    名称:
    N-versus O-silylation in cis-[(tBuHN)OP(μ-NtBu)2PO(NHtBu)] and [Me2Si(μ-NtBu)2PO(NHPh)]. Solid-state structures of their silylation products, of co-crystalline cis-[(tBuHN)OP(μ-NtBu)2PO(NHtBu)], and of {[Me2Si(μ-NtBu)2PO(N(SiMe3)Ph)]VCl3}
    摘要:
    The solid-state structure of cis-[((t)BuHN)O=P(mu-N(t)Bu)(2)P=O(NH(t)Bu)] (A), isolated as a 2-phenyl-2-propanol/ 2-phenyl-2-propanehydroperoxide co-crystal (1), is reported. Treatment of pure A with two equivalents of n-butyllithium, followed by addition of Me(3)SiCl, afforded the bis-O, O'-silylated cis-[( Me(3)SiO)(t)BuN=P(mu-N(t)Bu)(2)P=N(t)Bu(OSiMe(3))] (2), whose solid-state structure was determined. When the cyclic N,N,N-phosphoramidate [Me(2)Si(mu-N(t)Bu)(2)P=O(NHPh)] (B) was subjected to the same treatment as A, however, the N-silylated [Me(2)Si(mu-N(t)Bu)(2)P=O(N(SiMe(3))Ph)] (3), was obtained. Its solid-state structure was determined. The reaction of 3 with VCl(3)(THF)(3) did not produce the intended N, O-chelated V(II) complex, but furnished instead the adduct {[Me(2)Si(mu-N(t)Bu)(2)P=O(N(SiMe(3))Ph)] VCl(3)(THF)}, in which 3 binds the trigonal-bipyramidally coordinated vanadium center through its oxygen atom only. (c) 2008 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2008.05.023
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