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tetrakis[2-(tribromostannyl)ethyl]silane | 314727-94-1

中文名称
——
中文别名
——
英文名称
tetrakis[2-(tribromostannyl)ethyl]silane
英文别名
tetrakis[2-(tribromostannyl)ethylene]silane;tetrakis(2-tribromostannylethyl)silane
tetrakis[2-(tribromostannyl)ethyl]silane化学式
CAS
314727-94-1
化学式
C8H16Br12SiSn4
mdl
——
分子量
1573.99
InChiKey
HQWHXJOLRDWURS-UHFFFAOYSA-B
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

物化性质

  • 沸点:
    687.4±65.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    11.93
  • 重原子数:
    25
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 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:
    tetrakis[2-(tribromostannyl)ethyl]silane 在 LiAlH4 作用下, 以 乙醚 为溶剂, 以90%的产率得到tetrakis(2-stannylethyl)silane
    参考文献:
    名称:
    Si(CH2CH2SnH3)4—a unique organotin hydride featuring 12 SnH units in a dendritic molecule. Single-crystal X-ray structures of tetrakis(2-stannylethylene)silane and tetrakis[2-(triphenylstannyl)ethylene]silane
    摘要:
    Fourfold hydrostannation of tetravinylsilane affords the first generation metallodendrimer Si(CH2CH2SnPh3)(4) (1). Selective bromination yields Si(CH2CH2SnBr3)(4) (2), which can be reduced by LiAlH4 to give Si(CH2CH2SnH3)(4) (3), containing 12 reactive Sn-H bonds. These novel dendritic organotin compounds were characterized by elemental analysis, spectroscopic studies (H-1-, C-13-, Sn-119-NMR; IR) and by single-crystal X-ray structure determination. The molecular structures of 1 and 3 reveal increased conformational constraint in 1; the average Sn-H bond length in 3 is 1.60(7) Angstrom. (C) 2000 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0022-328x(00)00188-1
  • 作为产物:
    描述:
    tetrakis[2-(triphenylstannyl)ethylene]silane四氯化碳 为溶剂, 以71%的产率得到tetrakis[2-(tribromostannyl)ethyl]silane
    参考文献:
    名称:
    Si(CH2CH2SnH3)4—a unique organotin hydride featuring 12 SnH units in a dendritic molecule. Single-crystal X-ray structures of tetrakis(2-stannylethylene)silane and tetrakis[2-(triphenylstannyl)ethylene]silane
    摘要:
    Fourfold hydrostannation of tetravinylsilane affords the first generation metallodendrimer Si(CH2CH2SnPh3)(4) (1). Selective bromination yields Si(CH2CH2SnBr3)(4) (2), which can be reduced by LiAlH4 to give Si(CH2CH2SnH3)(4) (3), containing 12 reactive Sn-H bonds. These novel dendritic organotin compounds were characterized by elemental analysis, spectroscopic studies (H-1-, C-13-, Sn-119-NMR; IR) and by single-crystal X-ray structure determination. The molecular structures of 1 and 3 reveal increased conformational constraint in 1; the average Sn-H bond length in 3 is 1.60(7) Angstrom. (C) 2000 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0022-328x(00)00188-1
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文献信息

  • Synthesis and Characterization of Silicon-Based Group 14 Dendrimers Si{(CH<sub>2</sub>)<sub>2</sub>Sn[(CH<sub>2</sub>)<sub>4</sub>MPh<sub>3</sub>]<sub>3</sub>}<sub>4</sub> (M = Ge, Sn)
    作者:Herbert Schumann、Yilmaz Aksu
    DOI:10.1021/om060853l
    日期:2007.1.1
    hydrogermylation of Si(CHCH2)4 with Ph3GeH yielded Si(CH2CH2GePh3)4 (1). In contrast, Sn(CHCH2)4 and Sn(CH2CHCH2)4 reacted with Ph3GeH under the same conditions, forming Ph3Ge(CH2)2GePh3 (2) and Ph3Ge(CH2)3GePh3 (3), respectively, whereas the reaction of Sn(CH2CH2CHCH2)4 and Ph3GeH afforded the expected tin-based metallodendrimer Sn[(CH2)4GePh3]4 (4). The reactions of Si[(CH2)2SnBr3]4 with the Grignard reagents
    Si(CH CH 2)4与Ph 3 GeH的催化加氢锗化反应生成Si(CH 2 CH 2 GePh 3)4(1)。相反,Sn(CH CH 2)4和Sn(CH 2 CH CH 2)4在相同条件下与Ph 3 GeH反应,形成Ph 3 Ge(CH 2)2 GePh 3(2)和Ph 3 Ge(CH)2)3个GePh如图3(3)所示,而Sn(CH 2 CH 2 CH CH 2)4和Ph 3 GeH的反应提供了预期的锡基金属树枝状聚合物Sn [(CH 2)4 GePh 3 ] 4(4)。Si [(CH 2)2 SnBr 3 ] 4与格氏试剂RMgBr(R = CH CH 2,CH 2 CH CH 2,(CH 2)2 CH CH 2))生成Si [(CH 2)2 Sn(CH CH 2)3 ] 4(5),Si [(CH 2)2 Sn(CH 2 CH CH 2)3 ] 4(6)和Si [(CH 2)2 Sn(CH
  • Synthesis and characterization of new silicon-centred tin-dendrimers Si[CH2CH2SnR3]4. Single-crystal X-ray structure of the tetrahydrofuran adduct of tetrakis[2-(tribromostannyl)ethyl]silane
    作者:Herbert Schumann、Yilmaz Aksu、Stefan Schutte、Birgit C. Wassermann、Stefan H. Mühle
    DOI:10.1016/j.jorganchem.2006.07.017
    日期:2006.11
    A series of novel first-generation silicon-centred tin dendrimers Si(CH2CH2SnR3)(4) [R = CH3 (3), Bu-i (4), C CCH3 (5), C6H4CH3-4 (6), C6H4OCH3-4 (7), (CH2)(4)OCH2CH2OCH3 (8), CH2SiMe3 (9)] was prepared by the reaction of Si(CH2CH2SnBr3)(4) (2) with the appropriate Grignard reagent or LiCH2SiMe3 in tetrahydrofuran. The new compounds were characterized by multinuclear NMR studies (H-1, C-13, Sn-119), mass spectrometry (MALDI-TOF, EI) and elemental analyses. The molecular structure of Si[CH2CH2SnBr3(THF)(2)](2)[CH2CH2SnBr3(THF)](2) (2a) was determined by single-crystal X-ray diffraction. (c) 2006 Elsevier B.V. All rights reserved.
  • Si(CH2CH2SnH3)4—a unique organotin hydride featuring 12 SnH units in a dendritic molecule. Single-crystal X-ray structures of tetrakis(2-stannylethylene)silane and tetrakis[2-(triphenylstannyl)ethylene]silane
    作者:Herbert Schumann、Birgit C. Wassermann、Michaela Frackowiak、Bamidele Omotowa、Stefan Schutte、Janna Velder、Stefan H. Mühle、Werner Krause
    DOI:10.1016/s0022-328x(00)00188-1
    日期:2000.9
    Fourfold hydrostannation of tetravinylsilane affords the first generation metallodendrimer Si(CH2CH2SnPh3)(4) (1). Selective bromination yields Si(CH2CH2SnBr3)(4) (2), which can be reduced by LiAlH4 to give Si(CH2CH2SnH3)(4) (3), containing 12 reactive Sn-H bonds. These novel dendritic organotin compounds were characterized by elemental analysis, spectroscopic studies (H-1-, C-13-, Sn-119-NMR; IR) and by single-crystal X-ray structure determination. The molecular structures of 1 and 3 reveal increased conformational constraint in 1; the average Sn-H bond length in 3 is 1.60(7) Angstrom. (C) 2000 Elsevier Science S.A. All rights reserved.
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