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[(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)GaH3] | 1187968-85-9

中文名称
——
中文别名
——
英文名称
[(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)GaH3]
英文别名
(1,3-bis-(2,6-di-iso-propylphenyl)imidazolin-2-ylidene)·GaH3;(Dipp2Im)·GaH3
[(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)GaH3]化学式
CAS
1187968-85-9
化学式
C27H39GaN2
mdl
——
分子量
461.343
InChiKey
GCGZJYVCFARENE-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:
    [(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)GaH3]四氢呋喃甲苯 为溶剂, 反应 1.75h, 生成 [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene.GaH2PH2BH2.IDipp][triflate]
    参考文献:
    名称:
    NHC·GaH2(OTf) 加合物的一般途径——合成 NHC 稳定的镓阳离子 13/15 链化合物的关键
    摘要:
    报道了NHC 稳定的三氟甲磺酸镓 NHC ⋅ GaH 2 (OTf) (NHC=IDipp, IMes, IPr 2 Me 2 ) 的一般合成途径。这些化合物被用作构建块,以获得前所未有的 13/15 较重族 13 元素的阳离子链化合物 [IDipp ⋅ GaH 2 PR 2 EH 2  ⋅ D] (R=H, Ph; D=NMe 3 , IDipp; E=乙,加)。所有化合物均通过单晶 X 射线结构测定进行表征,并通过计算方法阐明电子特征。
    DOI:
    10.1002/chem.202301752
  • 作为产物:
    描述:
    lithium tetrahydridogallate 、 1,3-双(2,6-二异丙基苯基)咪唑-2-烯乙醚 为溶剂, 以76%的产率得到[(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)GaH3]
    参考文献:
    名称:
    N-heterocyclic carbene coordinated gallanes and chlorogallanes
    摘要:
    The preparation of the N-heterocyclic carbene coordinated gallium complexes [GaH3(IXy)] (1), [GaH3(IDipp)] (2), [GaClH2(IMes)] (3) and [GaCl2H(IMes)] (4), where IXy = 1,3-bis(2,6-dimethylphenyl)imidazol-2-ylidene, IDipp = 1,3-bis(2,6-diisopropylphenyl) imidazol-2-ylidene and IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene, are reported. All four complexes have been characterised by H-1, C-13 NMR and IR spectroscopy and, for complexes 2, 3 and 4, single crystal X-ray structure determination. These compounds represent some of the most thermally stable molecular gallium hydrides known, with 4 being the most thermally stable gallium hydride reported (dec. 274 degrees C). These remarkable thermal stabilities translate to significant aerobic stability such that all four compounds may be handled in dry air without significant decomposition. Compounds 2, 3 and 4 exist as distorted tetrahedra in the solid state with gallium to carbene C-donor bonds that shorten with increasing Lewis acidity of the gallium centre. Compound 2 co-crystallizes with 1 equiv. of 2,6-diisopropylphenylaniline and exhibits several weak intermolecular bonding interactions in the solid-state. (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2009.04.030
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文献信息

  • NHC‐stabilized Parent Arsanylalanes and ‐gallanes
    作者:Michael A. K. Weinhart、Michael Seidl、Alexey Y. Timoshkin、Manfred Scheer
    DOI:10.1002/anie.202013849
    日期:2021.2.15
    The synthesis and characterization of the unprecedented compounds IDipp⋅E′H2AsH2 (E′=Al, Ga; IDipp=1,3‐bis(2,6‐diisopropylphenyl)imidazolin‐2‐ylidene) are reported, the first monomeric, parent representatives of an arsanylalane and arsanylgallane, respectively, stabilized only by a LB (LB=Lewis Base). They are prepared by a salt metathesis reaction of KAsH2 with IDipp⋅E′H2Cl (E′=Al, Ga). The H2‐elimination
    报道了前所未有的化合物 IDipp⋅E′H 2 AsH 2 (E′=Al, Ga; IDipp=1,3-双(2,6-二异丙基苯基)咪唑啉-2-亚基)的合成和表征,这是第一个单体,分别是丙烷丙烷的母体代表,仅通过 LB(LB=路易斯碱)稳定。它们是通过 KAsH 2与 IDipp⋅E'H 2 Cl (E'=Al, Ga) 的盐复分解反应制备的。通过AsH 3与IDipp⋅E′H 3 (E′=Al, Ga)反应的H 2消除途径被发现是一种可能的合成路线,但与盐复分解反应相比存在一些缺点。通过KAsPh 2与IDipp⋅E′H 2 Cl (E′=Al, Ga)反应得到相应的有机取代化合物IDipp⋅GaH 2 AsPh 2 ( 1 ) 和IDipp⋅AlH 2 AsPh 2 ( 2 ) 。以IDipp⋅E′HCl 2 (E′=Al, Ga)为原料,通过盐复分解反应合成新型支化母体化合物IDipp⋅E′H(EH
  • Phosphanylalanes and Phosphanylgallanes Stabilized only by a Lewis Base
    作者:Michael A. K. Weinhart、Anna S. Lisovenko、Alexey Y. Timoshkin、Manfred Scheer
    DOI:10.1002/anie.201914046
    日期:2020.3.27
    The synthesis and characterization of the first parent phosphanylalane and phosphanylgallane stabilized only by a Lewis base (LB) are reported. The corresponding substituted compounds, such as IDipp⋅GaH2 PCy2 (1) (IDipp=1,3-bis(2,6-diisopropylphenyl)-imidazolin-2-ylidene) were obtained by the reaction of LiPCy2 with IDipp⋅GaH2 Cl. However, the LB-stabilized parent compounds IDipp⋅GaH2 PH2 (3) and IDipp⋅AlH2
    报道了第一母体膦酰丙烷和仅通过路易斯碱(LB)稳定的膦酰五倍子的合成和表征。LiPCy2与IDipp⋅GaH2 Cl反应得到相应的取代化合物,如IDipp⋅ PCy2 (1) (IDipp=1,3-双(2,6-二异丙基苯基)-咪唑啉-2-亚基)。然而,LB 稳定的母体化合物 IDipp⋅ PH2 (3) 和 IDipp⋅AlH2 PH2 (4) 是通过 LiPH2 ⋅DME 与 IDipp⋅E'H2 Cl (E'=Ga, Al) 的盐复分解制备的,或者通过分别为 IDipp⋅E'H3 (E'=Ga, Al) 和 PH3 的 H2 消除反应。这些化合物可以作为结晶固体分离出来并进行完全表征。支持 DFT 计算可以深入了解反应途径以及这些化合物在分解行为方面的稳定性。
  • N-Heterocyclic carbene and cyclic (alkyl)(amino)carbene adducts of gallium hydrides, gallium chlorides and gallium hydrochlorides
    作者:Andreas Hock、Luis Werner、Christian Luz、Udo Radius
    DOI:10.1039/d0dt02070b
    日期:——
    13 and Dipp2ImH14) and (cAACMe)·GaHCl215 is reported. Compounds 1–3 and 9–11 are unstable in solution as heating to the boiling temperature of toluene (110 °C) leads to decomposition into elemental gallium and the corresponding dihydroaminal NHC–H2. The reaction of the mono-NHC adducts with a second equivalent of NHC also afforded decomposition and formation of NHC–H2, whereas the reaction of the NHC-stabilized
    (NHC)·GaH 3型(NHC = Me 2 Im Me 1,iPr 2 Im 2)的N-杂环卡宾(NHC)和环状(烷基)(基)卡宾(cAAC)烷和gallane加合物的合成与表征,iPr 2 Im Me 3和Dipp 2 Im H 4; Me 2 Im Me = 1,3,4,5-四甲基-咪唑啉-2-亚基; R 2 Im = 1,3-二-有机基-咪唑啉- 2-亚烷基; Dipp = 2,6-二异丙基苯基; Dipp 2 Im H = 1,3-双(2,6-二异丙基苯基)-咪唑啉-2--2-亚烷基,(NHC)·GaH 2Cl(NHC = iPr 2 Im Me 9,Dipp 2 Im 10和Dipp 2 Im H 11 ; iPr 2 Im Me = 1,3二异丙基-4,5-二甲基咪唑啉-2-亚甲基),(NHC)·GaHCl 2据报道(NHC = iPr 2 Im Me 12,Dipp
  • Bis‐NHC Aluminium and Gallium Dihydride Cations [(NHC) <sub>2</sub> EH <sub>2</sub> ] <sup>+</sup> (E = Al, Ga)
    作者:Andreas Hock、Luis Werner、Melanie Riethmann、Udo Radius
    DOI:10.1002/ejic.202000720
    日期:2020.11.15
    treatment of (NHC)·GaH3 with an excess of methyl iodide at room temperature. The reaction of one equivalent of the group 13 NHC complexes with an additional equivalent of the corresponding NHC afforded cationic aluminium and gallium hydrides [(NHC)2·AlH2]+I− (NHC = Me2ImMe 13, iPr2Im 14, iPr2ImMe 15) and [(NHC)2·GaH2]+I− (NHC = Me2ImMe 16, iPr2ImMe 17) and the normal and abnormal NHC coordinated compound
    NHC烷和加仑烷加合物(NHC)· AlH 2 I(NHC = Me 2 Im Me 7,i Pr 2 Im 8,i Pr 2 Im Me 9)和(NHC)· GaH 2 I(NHC = Me 2 Im Me 7) 10,i Pr 2 Im Me 11,Dipp 2 Im 12 ; R 2 Im = 1,3-二有机基-咪唑啉-2-亚基; Dipp = 2,6-二异丙基苯基; i Pr =异丙基; Me2 Im Me = 1,3,4,5-四甲基-咪唑啉-2-亚基)是通过NHC加合物(NHC)· AlH 3与元素的简单而有效的反应或通过处理( NHC)·室温下含过量甲基的GaH 3。一当量的第13组NHC配合物与另一当量的相应NHC反应生成阳离子铝和氢化镓[(NHC)2 · AlH 2 ] + I-(NHC = Me 2 Im Me 13,i Pr 2 Im 14,i Pr 2 Im Me
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