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bis[di(tert-butyl)gallium(tert-butylhydrazide)] | 850804-56-7

中文名称
——
中文别名
——
英文名称
bis[di(tert-butyl)gallium(tert-butylhydrazide)]
英文别名
(t-Bu2GaNH-HNBu-t)2
bis[di(tert-butyl)gallium(tert-butylhydrazide)]化学式
CAS
850804-56-7;850940-43-1
化学式
C24H58Ga2N4
mdl
——
分子量
542.197
InChiKey
BFGBDULKWXFSNV-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:
    bis[di(tert-butyl)gallium(tert-butylhydrazide)] 以 neat (no solvent) 为溶剂, 以70%的产率得到{t-Bu2Ga(μ-NH2)}3
    参考文献:
    名称:
    寡核镓氮笼化合物:从氢化肼到氮化镓的分子中间体
    摘要:
    酰肼可潜在地用作通过热解生成GaN的简便起始化合物。然而,分解途径是复杂的,并且在很大程度上取决于与镓原子和肼基相连的取代基。本文介绍了一些系统的研究,以研究肼镓加合物Bu t 3 Ga←NH 2 -NHMe(1a)和二聚酰肼[R 2 Ga(N 2 H 2 R')] 2(2b,R = Bu t,R'= Bu t;2c,R = Pr i,R'= Ph; 2d,R = Me,R'= Bu t),它们的分子核中具有四元或五元杂环。加热所述加合物的1A至170℃,得到的杂环化合物卜吨2镓(μ-NH 2)[μ-N(Me)的-N(= CH 2)]加布吨2(3),通过N-N裂解键和重新排列。3进一步转化在400℃到四聚体镓氰化物(卜吨2 GaCN)4(4)。酰肼(Bu t 2 Ga)2(NH-NHBu t)2(2b的热解)在270和420之间的温度下℃下导致的所有N-N键的断裂和形成的octanucle
    DOI:
    10.1021/ic1019839
  • 作为产物:
    描述:
    叔丁基肼di(tert-butyl)gallium chloride 在 t-BuLi 作用下, 以 甲苯 为溶剂, 以32%的产率得到bis[di(tert-butyl)gallium(tert-butylhydrazide)]
    参考文献:
    名称:
    Adducts of organogallium chlorides with hydrazines and the formation of dimeric dialkylgallium hydrazides possessing different ring sizes
    摘要:
    The dialkylgallium chlorides R2GaCl (R = Me, Et, CMe3) reacted with hydrazines H2N-N(H)R' (R' = CMe3, C6H5) to form the adducts R2ClGa <- NH2-N(H)R' (1-4), in which the gallium atoms are coordinated by the NH2 nitrogen atoms of the hydrazine ligands. Treatment of these adducts with tert-butyllithium as a base afforded dialkylgallium hydrazides (R2Ga-N2H2R')(2) [5(R = R' = CMe3) and 6 (R = CMe3, R' = C6H5)] by deprotonation of the hydrazine ligands and precipitation of LiCl in two cases only. The remaining adducts gave a substitution reaction at gallium or an unclear reaction course. The hydrazides 5 and 6 adopt different structures in the solid state. The tri(tert-butyl) compound 5 possesses a four-membered Ga2N2 heterocycle in its molecular core with two exocyclic N-N bonds, which represents the structural motif usually observed for dialkylgallium hydrazides. 6 has a five-membered Ga2N3 heterocycle with one endocyclic and one exocyclic N-N bond. That structure is preserved in solution as clearly shown by NMR spectroscopy. The behaviour of 5 in solution is more complicated, which may be caused by cis/trans isomerization. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2004.12.021
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