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1,4-dilithio-1,1,4,4-tetra(tert-butyl)-tetramethyl-1,4-distanna-2,3-disilabutane | 339048-85-0

中文名称
——
中文别名
——
英文名称
1,4-dilithio-1,1,4,4-tetra(tert-butyl)-tetramethyl-1,4-distanna-2,3-disilabutane
英文别名
——
1,4-dilithio-1,1,4,4-tetra(tert-butyl)-tetramethyl-1,4-distanna-2,3-disilabutane化学式
CAS
339048-85-0
化学式
C20H48Li2Si2Sn2
mdl
——
分子量
596.074
InChiKey
JGLJDILZWWDNRC-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):
    6.53
  • 重原子数:
    26
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 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:
    1,4-dilithio-1,1,4,4-tetra(tert-butyl)-tetramethyl-1,4-distanna-2,3-disilabutane二苯二氯硅烷四氢呋喃 为溶剂, 以20%的产率得到3,3,5,5-tetra(tert-butyl)-1,1,2,2-tetramethyl-4,4-diphenyl-1,2,4-trisila-3,5-distannacyclopentane
    参考文献:
    名称:
    摘要:
    Dilithiated di(stannyl)oligosilanes ((Bu2Sn)-Bu-t(Li)-(SiMe2)(n)-Sn(Li)Bu-t(2); 4, n = 2; 5, n = 3) were synthesized by the reaction of lithium diisopropylamide (LDA) with the alpha,omega -hydrido tin substituted oligosilanes ((Bu2Sn)-Bu-t(H)-(SiMe2)(n)-Sn(H)Bu-t(2); 1, n = 2; 2, n = 3). Surprisingly, the reaction of 1 and 3 ((Bu2Sn)-Bu-t(H)-(SiMe2)(4)-Sn(H)Bu-t(2)) with LDA resulted not in the formation of the lithiated compound, but what one can find is the formation of the 5,5-ditert.butyl-octamethyl-1,2,3,4-tetrasila-5-stannacyclopentane (8) (n = 4) in addition to the expected product 4 (n = 4) and the 3,3,6,6-tetratert.butyl-octamethyl-1,2,4,5-tetrasila-3,6-distan-nacyclohexane (7) (n = 3).Reactions of 4 and 5 with dimethyl and diphenyldichlorosilanes yielding monocyclic Si-Sn derivatives (9-11) are also discussed. The solid-state structures of 7 and 11 were determined by X-ray crystallography.
    DOI:
    10.1002/1521-3749(200103)627:3<453::aid-zaac453>3.0.co;2-6
  • 作为产物:
    描述:
    1,1,4,4-tetra(tert-butyl)-tetramethyl-1,4-distanna-2,3-disilabutane 、 lithium diisopropyl amide四氢呋喃正己烷 为溶剂, 生成 1,1,2,2-tetra-tert-butyldistannane 、 1,4-dilithio-1,1,4,4-tetra(tert-butyl)-tetramethyl-1,4-distanna-2,3-disilabutane3,3,6,6-tetra(tert-butyl)-1,1,2,2,4,4,5,5-octamethyl-1,2,4,5-tetrasila-3,6-distannacyclohexane
    参考文献:
    名称:
    摘要:
    Dilithiated di(stannyl)oligosilanes ((Bu2Sn)-Bu-t(Li)-(SiMe2)(n)-Sn(Li)Bu-t(2); 4, n = 2; 5, n = 3) were synthesized by the reaction of lithium diisopropylamide (LDA) with the alpha,omega -hydrido tin substituted oligosilanes ((Bu2Sn)-Bu-t(H)-(SiMe2)(n)-Sn(H)Bu-t(2); 1, n = 2; 2, n = 3). Surprisingly, the reaction of 1 and 3 ((Bu2Sn)-Bu-t(H)-(SiMe2)(4)-Sn(H)Bu-t(2)) with LDA resulted not in the formation of the lithiated compound, but what one can find is the formation of the 5,5-ditert.butyl-octamethyl-1,2,3,4-tetrasila-5-stannacyclopentane (8) (n = 4) in addition to the expected product 4 (n = 4) and the 3,3,6,6-tetratert.butyl-octamethyl-1,2,4,5-tetrasila-3,6-distan-nacyclohexane (7) (n = 3).Reactions of 4 and 5 with dimethyl and diphenyldichlorosilanes yielding monocyclic Si-Sn derivatives (9-11) are also discussed. The solid-state structures of 7 and 11 were determined by X-ray crystallography.
    DOI:
    10.1002/1521-3749(200103)627:3<453::aid-zaac453>3.0.co;2-6
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文献信息

  • ——
    作者:Uwe Hermann、Gregor Reeske、Markus Schürmann、Frank Uhlig
    DOI:10.1002/1521-3749(200103)627:3<453::aid-zaac453>3.0.co;2-6
    日期:2001.3
    Dilithiated di(stannyl)oligosilanes ((Bu2Sn)-Bu-t(Li)-(SiMe2)(n)-Sn(Li)Bu-t(2); 4, n = 2; 5, n = 3) were synthesized by the reaction of lithium diisopropylamide (LDA) with the alpha,omega -hydrido tin substituted oligosilanes ((Bu2Sn)-Bu-t(H)-(SiMe2)(n)-Sn(H)Bu-t(2); 1, n = 2; 2, n = 3). Surprisingly, the reaction of 1 and 3 ((Bu2Sn)-Bu-t(H)-(SiMe2)(4)-Sn(H)Bu-t(2)) with LDA resulted not in the formation of the lithiated compound, but what one can find is the formation of the 5,5-ditert.butyl-octamethyl-1,2,3,4-tetrasila-5-stannacyclopentane (8) (n = 4) in addition to the expected product 4 (n = 4) and the 3,3,6,6-tetratert.butyl-octamethyl-1,2,4,5-tetrasila-3,6-distan-nacyclohexane (7) (n = 3).Reactions of 4 and 5 with dimethyl and diphenyldichlorosilanes yielding monocyclic Si-Sn derivatives (9-11) are also discussed. The solid-state structures of 7 and 11 were determined by X-ray crystallography.
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