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tris(methyl-d3)bis(trimethyl-l5-phosphaneyl)tantalum(VII) chloride | 1356933-94-2

中文名称
——
中文别名
——
英文名称
tris(methyl-d3)bis(trimethyl-l5-phosphaneyl)tantalum(VII) chloride
英文别名
——
tris(methyl-d3)bis(trimethyl-l5-phosphaneyl)tantalum(VII) chloride化学式
CAS
1356933-94-2
化学式
C9H27Cl2P2Ta
mdl
——
分子量
458.043
InChiKey
DQVHTBUFZGHYPW-MDDCIKNYSA-L
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:
    1,4-二氧六环氘代碘甲烷五氯化钽 、 zinc(II) chloride 、 三甲基膦 在 lithium 作用下, 以 乙醚 为溶剂, 以21%的产率得到tris(methyl-d3)bis(trimethyl-l5-phosphaneyl)tantalum(VII) chloride
    参考文献:
    名称:
    A New Class of Transition Metal Pincer Ligand: Tantalum Complexes that Feature a [CCC] X3-Donor Array Derived from a Terphenyl Ligand
    摘要:
    A new class of [CCC] X-3-donor pincer ligand for transition metals has been constructed via cyclometalation of a 2,6-di-p-tolylphenyl ([Ar-Tol2]) derivative. Specifically, addition of PMe3 to [Ar-Tol2]TaMe3Cl induces elimination of methane and formation of the pincer complex, [kappa(3)-Ar-Tol2]-Ta(PMe3)(2)MeCl (Tol' = C6H3Me), which may also be obtained by treatment of Ta(PMe3)(2)Me3Cl2 with [Ar-Tol2]Li. Solutions of [kappa(3)-Ar-Tol2]Ta(PMe3)(2)MeCl undergo ligand redistribution with the formation of [kappa(3)-Ar-Tol2]Ta(PMe3)(2)Me-2 and [kappa(3)-Ar-Tol2]Ta(PMe3)(2)Cl-2, which may also be synthesized by the reactions of [kappa(3)-Ar-Tol2]Ta(PMe3)(2)MeCl with MeMgBr and ZnCl2, respectively. Reduction of [kappa(3)-Ar-Tol2]Ta(PMe3)(2)Cl-2 with KC8 in benzene gives the benzene complex [kappa(3)-Ar-Tol2]-Ta(PMe3)(2)(eta(6)-C6H6) that is better described as a 1,4-cyclohexadienediyl derivative. Deuterium labeling employing Ta(PMe3)(2)-(CD3)(3)Cl-2 demonstrates that the pincer ligand is created by a pair of Ar-H/Ta-Me sigma-bond metathesis transformations, rather than by a mechanism that involves alpha-H abstraction by a tantalum methyl ligand.
    DOI:
    10.1021/ja210404x
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