2,3,3-trimethyl-4,7-bis[(triisopropylsilyl)ethynyl]-2,3,3-trimethyl-3H-indole | 928333-81-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 2,3,3-trimethyl-4,7-bis[(triisopropylsilyl)ethynyl]-2,3,3-trimethyl-3H-indole
• 英文别名: Tri(propan-2-yl)-[2-[2,3,3-trimethyl-4-[2-tri(propan-2-yl)silylethynyl]indol-7-yl]ethynyl]silane
• CAS: 928333-81-7
• 化学式: C₃₃H₅₃NSi₂
• 分子量: 519.962
• InChiKey: VSLKKHWDMGVAAZ-UHFFFAOYSA-N

物化性质

• 沸点：
  539.5±50.0 °C(Predicted)
• 密度：
  0.89±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  10.21
• 重原子数：
  36
• 可旋转键数：
  10
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  12.4
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  2,3,3-trimethyl-4,7-bis[(triisopropylsilyl)ethynyl]-2,3,3-trimethyl-3H-indole 在 三乙胺 作用下， 以 乙醇 、 乙腈 为溶剂， 反应 8.0h， 生成 Tri(propan-2-yl)-[2-[1',3',3'-trimethyl-4'-[2-tri(propan-2-yl)silylethynyl]spiro[chromene-2,2'-indole]-7'-yl]ethynyl]silane
  参考文献：
  名称：

  Opening a Spiropyran Ring by Way of an Exciplex Intermediate

  摘要：

  A molecular dyad has been synthesized in which the main chromophore is a 1,4-diethynylated benzene residue terminated with pyrene moieties, this latter unit acting as a single chromophore. A spiropyran group has been condensed to the central phenylene ring so as to position a weak electron donor close to the pyrene unit. Illumination of the pyrene-based chromophore leads to formation of a fluorescent exciplex in polar solvents but pyrene-like fluorescence is observed in nonpolar solvents. The exciplex has a lifetime of a few nanoseconds and undergoes intersystem crossing to the pyrene-like triplet state with low efficiency. Attaching a 4-nitrobenzene group to the open end of the spiropyran unit creates a new route for decay of the exciplex whereby the triplet state of the spiropyran is formed. Nonradiative decay of this latter species results in ring opening to form the corresponding merocyanine species. Rate constants for the various steps have been obtained from time-resolved fluorescence spectroscopy carried out over a modest temperature range. Under visible light illumination, the merocyanine form reverts to the original spiropyran geometry so that the cycle is closed. Energy transfer from the pyrene chromophore to the merocyanine unit leads to an increased rate of ring closure and serves to push the steady-state composition in favor of the spiropyran form.

  DOI：

  10.1021/jo062124l
• 作为产物：
  描述：

  2,5-二溴苯胺 在 四(三苯基膦)钯 盐酸 、 溶剂黄146 、 三乙胺 、 zinc(II) chloride 、 sodium nitrite 作用下， 以 甲苯 为溶剂， 反应 49.0h， 生成 2,3,3-trimethyl-4,7-bis[(triisopropylsilyl)ethynyl]-2,3,3-trimethyl-3H-indole
  参考文献：
  名称：

  Opening a Spiropyran Ring by Way of an Exciplex Intermediate

  摘要：

  A molecular dyad has been synthesized in which the main chromophore is a 1,4-diethynylated benzene residue terminated with pyrene moieties, this latter unit acting as a single chromophore. A spiropyran group has been condensed to the central phenylene ring so as to position a weak electron donor close to the pyrene unit. Illumination of the pyrene-based chromophore leads to formation of a fluorescent exciplex in polar solvents but pyrene-like fluorescence is observed in nonpolar solvents. The exciplex has a lifetime of a few nanoseconds and undergoes intersystem crossing to the pyrene-like triplet state with low efficiency. Attaching a 4-nitrobenzene group to the open end of the spiropyran unit creates a new route for decay of the exciplex whereby the triplet state of the spiropyran is formed. Nonradiative decay of this latter species results in ring opening to form the corresponding merocyanine species. Rate constants for the various steps have been obtained from time-resolved fluorescence spectroscopy carried out over a modest temperature range. Under visible light illumination, the merocyanine form reverts to the original spiropyran geometry so that the cycle is closed. Energy transfer from the pyrene chromophore to the merocyanine unit leads to an increased rate of ring closure and serves to push the steady-state composition in favor of the spiropyran form.

  DOI：

  10.1021/jo062124l

文献信息

• Opening a Spiropyran Ring by Way of an Exciplex Intermediate
  作者：Andrew C. Benniston、Anthony Harriman、Sarah L. Howell、Peiyi Li、Donocadh P. Lydon

  DOI：10.1021/jo062124l

  日期：2007.2.1

  A molecular dyad has been synthesized in which the main chromophore is a 1,4-diethynylated benzene residue terminated with pyrene moieties, this latter unit acting as a single chromophore. A spiropyran group has been condensed to the central phenylene ring so as to position a weak electron donor close to the pyrene unit. Illumination of the pyrene-based chromophore leads to formation of a fluorescent exciplex in polar solvents but pyrene-like fluorescence is observed in nonpolar solvents. The exciplex has a lifetime of a few nanoseconds and undergoes intersystem crossing to the pyrene-like triplet state with low efficiency. Attaching a 4-nitrobenzene group to the open end of the spiropyran unit creates a new route for decay of the exciplex whereby the triplet state of the spiropyran is formed. Nonradiative decay of this latter species results in ring opening to form the corresponding merocyanine species. Rate constants for the various steps have been obtained from time-resolved fluorescence spectroscopy carried out over a modest temperature range. Under visible light illumination, the merocyanine form reverts to the original spiropyran geometry so that the cycle is closed. Energy transfer from the pyrene chromophore to the merocyanine unit leads to an increased rate of ring closure and serves to push the steady-state composition in favor of the spiropyran form.