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(SiMe3)3CAlMe2(THF) | 201054-44-6

中文名称
——
中文别名
——
英文名称
(SiMe3)3CAlMe2(THF)
英文别名
aluminum;bis(trimethylsilyl)methyl-trimethylsilane;carbanide;oxolane
(SiMe3)3CAlMe2(THF)化学式
CAS
201054-44-6
化学式
C4H8O*C12H33AlSi3
mdl
——
分子量
360.739
InChiKey
HULBGUWBSXPAOW-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

  • 作为反应物:
    描述:
    (SiMe3)3CAlMe2(THF)三氟乙酸甲苯 为溶剂, 以10%的产率得到[Al3(μ3-O)(μ-CF3CO2)6(tetrahydrofuran)3][(Me3Si)3CAl(CF3CO2)3]*C6H5CH3
    参考文献:
    名称:
    Lightest Member of the Basic Carboxylate Structural Pattern:  [Al33-O)(μ-O2CCF3)6(THF)3][(Me3Si)3CAl(O2CCF3)3]·C7H8
    摘要:
    [Al-3(mu(3)-O)(mu-O2CCF3)(6)(THF)(3)][(Me3Si)(3)CAl( OC(O)CF3)(3)]-C7H8 is the first characterized mu3-oxo-trinuclear basic carboxylate of aluminum closing the gap of isomorphism with the transition metal analogues. The system is an excellent case study for the electronic structure approached by DFT-B3LYP calculations. The actual system proves that the oxo-trinuclear pattern is stabilized by the chemical hardness of oxygen donors and by highly symmetric intramolecular packing of the ligands.
    DOI:
    10.1021/ic010880y
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文献信息

  • Reactions of [(Me3Si)3CAlMe2] with substituted benzoic acids. Isolation of a rare organoalumoxane carboxylate
    作者:Laksheswar Kalita、Ramasamy Pothiraja、Vaibhav Saraf、Mrinalini G. Walawalkar、Ray J. Butcher、Ramaswamy Murugavel
    DOI:10.1016/j.jorganchem.2011.06.024
    日期:2011.10
    bulky tris(trimethylsilyl)methyl group substituted aluminum trialkyl [(Me3Si)3CAlMe2·THF] (1) with a series of substituted benzoic acid derivatives has been investigated. An equimolar reaction of 4-methyl benzoic acid or 4-tert-butyl benzoic acid with 1 in toluene at 50 °C leads to the formation of cyclic dimeric aluminum carboxylates [(Me3Si)3CAl(Me)(μ-O2CC6H4R)]2 (R = Me 2; tBu 3). Reaction of 3,
    研究了大体积的被三(三甲基甲硅烷基)甲基取代的三烷基铝[(Me 3 Si)3 CAlMe 2 ·THF](1)与一系列取代的苯甲酸生物的反应性。的4-甲基苯甲酸或4-等摩尔反应叔丁基苯甲酸与1在甲苯中在50℃下导致形成环状二聚羧酸铝的[(ME 3 Si)的3的CA1(ME)(μ-O 2 CC 6 H 4 R)] 2(R = Me 2;t Bu 3)。3,5-二异氰酸酯的反应带有1的-丙基水杨酸(H 2 dipsa)导致三聚体有机铝羧酸盐[(Me 3 Si)3 CAl(μ-dipsa)] 3(4)的唯一分离,其中每个铝与两个羧酸盐结合,和一个烷基,生成一个12元大环。在甲苯中与1进行反应时,故意但有控制地引入3,5-二叔丁基水杨酸合物(H 2 dtbsa·H 2 O)形式的,导致羧酸盐[[Me 3 Si)3 CAl(μ-O)(μ-Hdtbsa)} 2 ](5)具有双环结构。化合物5
  • Synthesis and Structures of [((Me<sub>3</sub>Si)<sub>3</sub>CAlF<sub>2</sub>)<sub>2</sub>(<i>μ</i>-O)Li<sub>2</sub>(THF)<sub>4</sub>] and [{Li(Me<sub>3</sub>Si)<sub>3</sub>CAlF<sub>3</sub>(THF)}<sub>3</sub>LiF(THF)]
    作者:Hagen Hatop、Marcus Schiefer、Herbert W. Roesky、Regine Herbst-Irmer、Thomas Labahn
    DOI:10.1021/om0100941
    日期:2001.6.1
    The synthesis of [((Me3Si)(3)CAlF2)(2)(mu -O)Li-2- (THF)(4)] (1) and [Li(Me3Si)(3)CAlF3(THF)}(3)LiF(THF)] (2) is reported. Compound 1 was obtained either by the reaction of (Me3Si)(3)CAlMe2. THF and Me3SnF in the presence of Li2O or by the reaction of [(Me3Si)(3)CAlF2](3) and Li2O. 1 is an interesting example of an oxygen- and fluorine-containing alkyl aluminum compound. Complex 2 was prepared by the reaction of (Me3Si)(3)CAlF2. THF with LiOCH(CF3)(2) as an unexpected result that illustrates the variety of possible structures obtainable by the combination of [(Me3Si)(3)CAlF2](3) and LiF.
  • Klemp, Andreas; Hatop, Hagen; Roesky, Herbert W., Inorganic Chemistry, 1999, vol. 38, # 25, p. 5832 - 5836
    作者:Klemp, Andreas、Hatop, Hagen、Roesky, Herbert W.、Schmidt, Hans-Georg、Noltemeyer, Mathias
    DOI:——
    日期:——
  • Reactions of Dimethyl[tris(trimethylsilyl)methyl]metalanes of Aluminum and Gallium with H2S and Elemental Chalcogens – Crystal Structures of [RAl(μ-S)]2·2 THF, [RGa(μ3-S)]4, [{RAl(μ3-S)}3MeAl(μ3-S)], [RAlMe(μ-SeMe)]2, and [RGaMe(μ-TeMe)]2 [R = C(SiMe3)3]
    作者:Christoph Schnitter、Andreas Klemp、Herbert W. Roesky、Hans-Georg Schmidt、Cord Röpken、Regine Herbst-Irmer、Mathias Noltemeyer
    DOI:10.1002/(sici)1099-0682(199812)1998:12<2033::aid-ejic2033>3.0.co;2-i
    日期:1998.12
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