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Sb2(iBu)4 | 649560-57-6

中文名称
——
中文别名
——
英文名称
Sb2(iBu)4
英文别名
——
Sb2(iBu)4化学式
CAS
649560-57-6
化学式
C16H36Sb2
mdl
——
分子量
471.962
InChiKey
JLYGFHNMHKLLAP-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):
    5.14
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 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:
    Sb2(iBu)4三-叔-丁基铝正戊烷 为溶剂, 以92%的产率得到[tBu3Al]2[Sb2iBu)4]
    参考文献:
    名称:
    Reactions of Group 13 Organometallics t Bu 3 M with Distibanes Sb 2 R 4
    摘要:
    AbstractTetraalkyldistibanes Sb2R4 (R = nPr, iBu) react with tBu3M (M = Al, Ga) at –30 °C with the formation of the Lewis acid–base adducts [tBu3M]2[Sb2R4] [M = Al, R = nPr (1), iBu (2); M = Ga, R = nPr (3), iPr 4)]. Compounds 1 and 2 are stable in solution whereas 3 undergoes a Sb–Sb bond‐breakage reaction with the subsequent formation of [tBu2GaSb(nPr)2]2 (5). The same trend was observed for the reaction of Sb2(iBu)4 with tBu3Ga, which yielded the heterocyclic stibanylgallane [tBu2GaSb(iBu)2]2 (6). In addition, the simple trialkylstibane adduct tBu3Al–Sb(iBu)3 (7) was obtained as a byproduct from the reaction of Sb2(iBu)4 with tBu3Al. Compounds 17 were characterized by multinuclear NMR (1H, 13C{1H}) and mass spectroscopy and elemental analysis. Compounds 1, 3, 5, and 7 were also investigated by single‐crystal X‐ray diffraction. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
    DOI:
    10.1002/ejic.200600976
  • 作为产物:
    描述:
    (isobutyl)2SbBr 在 Mg 、 1,2-dibromoethane 作用下, 以 四氢呋喃 为溶剂, 以48.8%的产率得到Sb2(iBu)4
    参考文献:
    名称:
    Syntheses of isobutylantimony compounds, cyclo-RnSbn (n=4, 5), R4Sb2, and crystal structure of R3SbBr2; R=Me2CHCH2
    摘要:
    Dehalogenation reactions of RSbBr2 or R2SbBr (R = Me2CHCH2) with Mg in tetrahydrofuran give cyclo-RnSbn(1, n = 4, 5) or R4Sb2 (2). R3SbBr2 (3) is formed by addition of Br-2 to R3Sb. The crystals of 3 consist of trigonal bipyramidal molecules with apical bromine atoms. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0277-5387(03)00333-4
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文献信息

  • Reactions of Group 13 Organometallics <i>t</i> Bu <sub>3</sub> M with Distibanes Sb <sub>2</sub> R <sub>4</sub>
    作者:Daniella Schuchmann、Andreas Kuczkowski、Sonja Fahrenholz、Stephan Schulz、Ulrich Flörke
    DOI:10.1002/ejic.200600976
    日期:2007.3
    AbstractTetraalkyldistibanes Sb2R4 (R = nPr, iBu) react with tBu3M (M = Al, Ga) at –30 °C with the formation of the Lewis acid–base adducts [tBu3M]2[Sb2R4] [M = Al, R = nPr (1), iBu (2); M = Ga, R = nPr (3), iPr 4)]. Compounds 1 and 2 are stable in solution whereas 3 undergoes a Sb–Sb bond‐breakage reaction with the subsequent formation of [tBu2GaSb(nPr)2]2 (5). The same trend was observed for the reaction of Sb2(iBu)4 with tBu3Ga, which yielded the heterocyclic stibanylgallane [tBu2GaSb(iBu)2]2 (6). In addition, the simple trialkylstibane adduct tBu3Al–Sb(iBu)3 (7) was obtained as a byproduct from the reaction of Sb2(iBu)4 with tBu3Al. Compounds 17 were characterized by multinuclear NMR (1H, 13C1H}) and mass spectroscopy and elemental analysis. Compounds 1, 3, 5, and 7 were also investigated by single‐crystal X‐ray diffraction. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
  • Syntheses of isobutylantimony compounds, cyclo-RnSbn (n=4, 5), R4Sb2, and crystal structure of R3SbBr2; R=Me2CHCH2
    作者:Lucia Balázs、Gabor Balázs、Hans J. Breunig、Ioan Ghesner、Enno Lork
    DOI:10.1016/s0277-5387(03)00333-4
    日期:2003.7
    Dehalogenation reactions of RSbBr2 or R2SbBr (R = Me2CHCH2) with Mg in tetrahydrofuran give cyclo-RnSbn(1, n = 4, 5) or R4Sb2 (2). R3SbBr2 (3) is formed by addition of Br-2 to R3Sb. The crystals of 3 consist of trigonal bipyramidal molecules with apical bromine atoms. (C) 2003 Elsevier Science Ltd. All rights reserved.
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