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di-tert-butylindium chloride | 92089-77-5

中文名称
——
中文别名
——
英文名称
di-tert-butylindium chloride
英文别名
Di-tert-butylindiumchlorid;(tert-butyl)2InCl
di-tert-butylindium chloride化学式
CAS
92089-77-5
化学式
C8H18ClIn
mdl
——
分子量
264.504
InChiKey
OSIBXWXZFRPKAD-UHFFFAOYSA-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):
    3.82
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    di-tert-butylindium chloride叔丁基肼甲苯 为溶剂, 以45%的产率得到(tert-butylhydrazine)di(tert-butyl)indium chloride
    参考文献:
    名称:
    Hydrazin-Addukte mit Dialkylindiumchloriden—Überraschende strukturelle Vielfalt bei einfachen Verbindungen
    摘要:
    二烷基氯化铟试剂 mit Hydrazinderivaten zu unterschiedlichen Addukten, die eine bemerkenswerte strukturelle Vielfalt zeigen。Die aquimolare Umsetzung von Me2InCl mit Phenylhydrazin ergibt das erwartete Monoaddukt [Me2InCl·NH2NHC6H5] (1), in dem der Ligand uber sein NH2-Stickstoffatom an das zentrale ergibt das erwartete Monoaddukt . Bei der entsprechende Reaktion mit tert-Butylhydrazin entsteht dagegen unter
    DOI:
    10.1002/zaac.200300197
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文献信息

  • Cyclopentadiene Elimination Reactions for the Preparation of Organoindium(III) Derivatives. Crystal and Molecular Structures of Me<sub>2</sub>In(acac), (Me<sub>3</sub>CCH<sub>2</sub>)<sub>2</sub>In(acac), (Me)(Me<sub>3</sub>CCH<sub>2</sub>)In(acac), and [Me<sub>2</sub>InNH(t-Bu)]<sub>2</sub>
    作者:O. T. Beachley,、David J. MacRae、Melvyn Rowen Churchill、Andrey Yu. Kovalevsky、Eric S. Robirds
    DOI:10.1021/om0304154
    日期:2003.9.1
    The compounds R2InO(t-Bu), R2In(acac), R2InSSiPh3, and R2InPPh2 (R = Me, CH2CMe3) and Me2InNH(t-Bu) have been prepared in nearly quantitative yields by the cyclopentadiene elimination reaction between R2In(C5H5) and the appropriate alcohol, thiol, phosphine or amine. All reactions except those of H2N(t-Bu) occur readily at room temperature. Even though solutions of R2In(C5H5) exist as equilibrium mixtures of R2In(C5H5), RIn(C5H5)(2), In(C5H5)(3), and InR3, neither methane nor neopentane was observed as a product from the above reaction mixtures. A ligand redistribution reaction between Me2In(C5H5) and (Me3CCH2)(2)In(C5H5) was used to prepare (Me)(Me)(Me3CCH2)In(C5H5) that, in turn, was reacted with H(acac) to form (Me)(Me3CCH2)In(acac), an indium compound with three different substituents. The compounds Me2In(acac), (Me3CCH2)(2)In(acac), and (Me)(Me3CCH2)In(acac) exist as centrosymmetric dimers in the solid state, but in benzene solution Me2In(acac) is a monomer-dimer equilibrium mixture, whereas (Me3CCH2)(2)In(acac) is a monomer. The thiolate Me2InSSiPh3 is an equilibrium mixture of dimers and trimers in benzene solution, but (Me3CCH2)(2)InSSiPh3 is a dimer. The phosphide Me2InPPh2 is an equilibrium mixture of monomers and dimers when dissolved in benzene. The tert-butylamide Me2InNH(t-Bu), when dissolved in benzene, is a mixture of monomers and dimers with both cis and trans configurations, but only a dimer with the trans configuration exists in the solid state.
  • Schumann, Herbert; Mohtachemi, Reza, Zeitschrift fur Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1984, vol. 39, # 6, p. 798 - 800
    作者:Schumann, Herbert、Mohtachemi, Reza
    DOI:——
    日期:——
  • Stoll, Sarah L.; Bott, Simon G.; Barron, Andrew R., Journal of the Chemical Society, Dalton Transactions, 1997, # 8, p. 1315 - 1321
    作者:Stoll, Sarah L.、Bott, Simon G.、Barron, Andrew R.
    DOI:——
    日期:——
  • Petrie, MA.; Ruhlandt-Senge, K.; Hope, H., Bulletin de la Societe Chimique de France, 1993, vol. 130, p. 851 - 855
    作者:Petrie, MA.、Ruhlandt-Senge, K.、Hope, H.、Power, PP.
    DOI:——
    日期:——
  • SCHUMANN, H.;MOHTACHEMI, R., Z. NATURFORSCH., 1984, 39, N 6, 798-800
    作者:SCHUMANN, H.、MOHTACHEMI, R.
    DOI:——
    日期:——
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