n-heptylphenyldichlorosilane

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: n-heptylphenyldichlorosilane
• 英文别名: Dichloro-heptyl-phenylsilane；dichloro-heptyl-phenylsilane
• 化学式: C₁₃H₂₀Cl₂Si
• 分子量: 275.293
• InChiKey: NAPUIWXCWYCBGL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.78
• 重原子数：
  16
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.54
• 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：

  n-heptylphenyldichlorosilane 在 copper(l) cyanide 、 臭氧 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 1.0h， 生成
  参考文献：
  名称：

  不对称烯胺催化高对映选择性构建多功能硅立构硅环

  摘要：

  报道了通过不对称烯胺催化对映选择性构建硅立体中心。该反应通过前手性 siladials 前所未有的不对称分子内醛缩化反应进行，用于多功能硅-立体硅环的多样化合成。

  DOI：

  10.1002/anie.202217724
• 作为产物：
  描述：

  HEPTYLMAGNESIUM BROMIDE 、 苯基三氯硅烷 以 四氢呋喃 为溶剂， 反应 2.0h， 生成 n-heptylphenyldichlorosilane
  参考文献：
  名称：

  Dynamics of Positive Charge Carriers on Si Chains of Polysilanes

  摘要：

  The transient absorption of radical cations of a variety of substituted polysilanes is discussed quantitatively in terms of the molar extinction coefficient and oscillator strength by nanosecond pulse radiolysis. Oxygen -saturated polysilane solutions in benzene exhibit a strong transient absorption band ascribed to the polysilane radical cation. The transient species react with N,N,N,N-tetramethyl-p-phenylenediamine (TMPD) to produce TMPD radical cations. On the basis of the molar extinction coefficient of the TMPD radical cation, the molar extinction coefficients for the radical cations of polysilanes are found to increase in the range 3.3 x 10(4) to 2.0 x 10(5) M(-1) cm(-1) with increasing polymer segment length. The stepwise increase in the total oscillator strength with an increase in the number of phenyl rings directly bonded to the Si skeleton suggests the delocalization of the positive polaron state and/or the SOMO state over the phenyl rings, indicating the importance of phenyl rings in intermolecular hole transfer processes.

  DOI：

  10.1021/ja039840e

文献信息

• Dynamics of Positive Charge Carriers on Si Chains of Polysilanes
  作者：Shu Seki、Yoshiko Koizumi、Tomoyo Kawaguchi、Hidefumi Habara、Seiichi Tagawa

  DOI：10.1021/ja039840e

  日期：2004.3.1

  The transient absorption of radical cations of a variety of substituted polysilanes is discussed quantitatively in terms of the molar extinction coefficient and oscillator strength by nanosecond pulse radiolysis. Oxygen -saturated polysilane solutions in benzene exhibit a strong transient absorption band ascribed to the polysilane radical cation. The transient species react with N,N,N,N-tetramethyl-p-phenylenediamine (TMPD) to produce TMPD radical cations. On the basis of the molar extinction coefficient of the TMPD radical cation, the molar extinction coefficients for the radical cations of polysilanes are found to increase in the range 3.3 x 10(4) to 2.0 x 10(5) M(-1) cm(-1) with increasing polymer segment length. The stepwise increase in the total oscillator strength with an increase in the number of phenyl rings directly bonded to the Si skeleton suggests the delocalization of the positive polaron state and/or the SOMO state over the phenyl rings, indicating the importance of phenyl rings in intermolecular hole transfer processes.
• Highly Enantioselective Construction of Multifunctional Silicon‐Stereogenic Silacycles by Asymmetric Enamine Catalysis
  作者：Xue‐Xin Zhang、Yang Gao、Yan‐Xue Zhang、Jian Zhou、Jin‐Sheng Yu

  DOI：10.1002/anie.202217724

  日期：2023.2.20

  The enantioselective construction of silicon-stereocenter by asymmetric enamine catalysis is reported. The reaction proceeds via an unprecedented desymmetric intramolecular aldolization of prochiral siladials for the diverse synthesis of multifunctional silicon-stereogenic silacycles.

  报道了通过不对称烯胺催化对映选择性构建硅立体中心。该反应通过前手性 siladials 前所未有的不对称分子内醛缩化反应进行，用于多功能硅-立体硅环的多样化合成。