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[Cl2AlO2CtBu]2 | 1353582-24-7

中文名称
——
中文别名
——
英文名称
[Cl2AlO2CtBu]2
英文别名
——
[Cl2AlO2CtBu]2化学式
CAS
1353582-24-7
化学式
C10H18Al2Cl4O4
mdl
——
分子量
398.026
InChiKey
XUHFVZQIXJFDAY-UHFFFAOYSA-H
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:
    4-甲基吡啶[Cl2AlO2CtBu]2二氯甲烷 为溶剂, 以92%的产率得到[Cl2Al(λ2-O2CtBu)(4-methylpyridine)2]
    参考文献:
    名称:
    Investigations on the Interaction of Dichloroaluminum Carboxylates with Lewis Bases and Water: an Efficient Road toward Oxo- and Hydroxoaluminum Carboxylate Complexes
    摘要:
    A series of dichloroaluminum carboxylates [Cl2Al(O2CR)](2) (were R = Ph (1a), Bu-t (1b), CHCH2 (1c) and C11H23 (Id)) were prepared and extended investigations on their structure and reactivity toward various Lewis bases and H2O performed. Compounds [Cl2Al(O2CR)](2) and their adducts with Lewis bases show a large structural variety, featuring both molecular and ionic forms with different coordination numbers of the metal center and various coordination modes of the carboxylate ligand. Upon addition of a Lewis base of moderate strength the molecular form [Cl2Al(O2CR)](2) equilibrates with new ionic forms. In the presences of 4-methylpyridine the six-coordinate Lewis acid-base adducts [Cl2Al(lambda(2)-O2CR)(py-Me)(2)] [R = Ph (3a), Bu-t (3b)] with a chelating carboxylate ligand were formed. The reactions of la, 1b, and Id with 0.33 equiv of H2O in THF-toluene solution lead to oxo carboxylates [(Al3O)(O2CR)(6)(THF)(3)] [AlCl4] [where R = Ph (4a(THF)), Bu-t (4b(THF)), and C11H23 (4d(THF))] in high yield. The similar reaction of 1c in tetrahydrofuran (THF) afforded the chloro(hydroxo)aluminum acrylate [(ClAl)(2)(OH)-(O2CC2H3)(2) (THF)4][AlCl4] (5), while the hydrolysis of 1b in MeCN lead to the hydroxoaluminum carboxylate [Al-2(OH)((O2CBu)-Bu-t)(2)(MeCN)(6)][AlCl4)(3)] (6). All compounds were characterized by elemental analysis, H-1, Al-27 NMR, and IR spectroscopy, and the molecular structure of 1a, 3a, 3b, 4aTHF, 4bTHF, 4b(py-Me'),, 5, and 6 were determined by single-crystal X-ray diffraction. The study provides a platform for testing transformations of secondary building units in Al-Metal-Organic Frameworks toward H2O and neutral donor ligands.
    DOI:
    10.1021/ic2023924
  • 作为产物:
    描述:
    二氯乙基铝三甲基乙酸甲苯 为溶剂, 以86%的产率得到[Cl2AlO2CtBu]2
    参考文献:
    名称:
    Investigations on the Interaction of Dichloroaluminum Carboxylates with Lewis Bases and Water: an Efficient Road toward Oxo- and Hydroxoaluminum Carboxylate Complexes
    摘要:
    A series of dichloroaluminum carboxylates [Cl2Al(O2CR)](2) (were R = Ph (1a), Bu-t (1b), CHCH2 (1c) and C11H23 (Id)) were prepared and extended investigations on their structure and reactivity toward various Lewis bases and H2O performed. Compounds [Cl2Al(O2CR)](2) and their adducts with Lewis bases show a large structural variety, featuring both molecular and ionic forms with different coordination numbers of the metal center and various coordination modes of the carboxylate ligand. Upon addition of a Lewis base of moderate strength the molecular form [Cl2Al(O2CR)](2) equilibrates with new ionic forms. In the presences of 4-methylpyridine the six-coordinate Lewis acid-base adducts [Cl2Al(lambda(2)-O2CR)(py-Me)(2)] [R = Ph (3a), Bu-t (3b)] with a chelating carboxylate ligand were formed. The reactions of la, 1b, and Id with 0.33 equiv of H2O in THF-toluene solution lead to oxo carboxylates [(Al3O)(O2CR)(6)(THF)(3)] [AlCl4] [where R = Ph (4a(THF)), Bu-t (4b(THF)), and C11H23 (4d(THF))] in high yield. The similar reaction of 1c in tetrahydrofuran (THF) afforded the chloro(hydroxo)aluminum acrylate [(ClAl)(2)(OH)-(O2CC2H3)(2) (THF)4][AlCl4] (5), while the hydrolysis of 1b in MeCN lead to the hydroxoaluminum carboxylate [Al-2(OH)((O2CBu)-Bu-t)(2)(MeCN)(6)][AlCl4)(3)] (6). All compounds were characterized by elemental analysis, H-1, Al-27 NMR, and IR spectroscopy, and the molecular structure of 1a, 3a, 3b, 4aTHF, 4bTHF, 4b(py-Me'),, 5, and 6 were determined by single-crystal X-ray diffraction. The study provides a platform for testing transformations of secondary building units in Al-Metal-Organic Frameworks toward H2O and neutral donor ligands.
    DOI:
    10.1021/ic2023924
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