(E)-dimethyl[3,5-bis(trifluoromethyl)phenyl]styrylsilane | 439659-78-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (E)-dimethyl[3,5-bis(trifluoromethyl)phenyl]styrylsilane
• 英文别名: [3,5-bis(trifluoromethyl)phenyl]-dimethyl-[(E)-2-phenylethenyl]silane
• CAS: 439659-78-6
• 化学式: C₁₈H₁₆F₆Si
• 分子量: 374.401
• InChiKey: DBSZWOPESHEUCZ-CMDGGOBGSA-N

物化性质

• 沸点：
  336.3±42.0 °C(Predicted)
• 密度：
  1.21±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.89
• 重原子数：
  25
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  (E)-dimethyl[3,5-bis(trifluoromethyl)phenyl]styrylsilane 在 bis(η3-allyl-μ-chloropalladium(II)) 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 反应 35.0h， 生成 (E)-2,5-dioctyloxy-4'-[(E)-2,5-dioctyloxy-4-[(E)-styryl]styryl]-stilbene
  参考文献：
  名称：

  通过钯催化的交叉偶联反应立体选择性合成顺式和反式（亚苯基亚乙烯基）

  摘要：

  顺式-低聚（亚苯基亚乙烯基）（OPV）是通过芳族硼酸与（Z）-溴代烯烃的Suzuki-Miyaura偶联以96％以上的几何纯度合成的。另一方面，反式-低聚（亚苯基亚乙烯基）可以通过芳基碘化物与（E）-烯基硅烷的Hiyama偶联以几乎完美的纯度来合成。描述了π共轭链长度对OPVs光异构化行为的影响。

  DOI：

  10.1021/jo052602c
• 作为产物：
  描述：

  [3,5-bis(trifluoromethyl)phenyl]dimethylsilane 、 苯乙炔 在 hydridochlorotris(triphenylphosphine)ruthenium(II) 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 生成 (E)-dimethyl[3,5-bis(trifluoromethyl)phenyl]styrylsilane
  参考文献：
  名称：

  Ruthenium-catalyzed hydrosilylation of terminal alkynes: stereodivergent synthesis of (E)- and (Z)-alkenylsilanes

  摘要：

  Stereodivergent hydrosilylation of terminal alkynes (RCequivalent toCH; R = Ph, p-tolyl, Cy, n-hexyl) with hydrosilanes (HSiMe2Ar; Arequivalent toPh, 3.5-(CF3)(2)C6H3, 4-CFC3H4, 4-MeOC6H4) has been examined using ruthenium catalysts. (E)-selective reactions giving (E)-RCH=CHSiMe2Ar proceed in over 99% selectivity in the presence of a catalytic amount of RuHCl(CO)(PPh3)(3). On the other hand, (Z)-selective reactions are successfully conducted in 91-99% selectivity by using Ru(SiMe2Ph)Cl(CO)(PPr'(3))(2) as the catalyst. All reactions readily proceed at room temperature in high yields. (E)- and (Z)-styrylsilanes having a SiMe2[C6H3-3,5-(CF3)(2)] group serve as good cross-coupling reagents with p-iodotoluene in the presence of tetrabutylammonium. fluoride and [Pd(eta(3)-al-lyl)Cl](2) catalyst. (C) 2002 Elsevier Science B.V. All rights reserved.

  DOI：

  10.1016/s0022-328x(01)01319-5

文献信息

• Ruthenium-catalyzed hydrosilylation of terminal alkynes: stereodivergent synthesis of (E)- and (Z)-alkenylsilanes
  作者：Hiroyuki Katayama、Ken Taniguchi、Masayuki Kobayashi、Takashi Sagawa、Tatsuya Minami、Fumiyuki Ozawa

  DOI：10.1016/s0022-328x(01)01319-5

  日期：2002.2

  Stereodivergent hydrosilylation of terminal alkynes (RCequivalent toCH; R = Ph, p-tolyl, Cy, n-hexyl) with hydrosilanes (HSiMe2Ar; Arequivalent toPh, 3.5-(CF3)(2)C6H3, 4-CFC3H4, 4-MeOC6H4) has been examined using ruthenium catalysts. (E)-selective reactions giving (E)-RCH=CHSiMe2Ar proceed in over 99% selectivity in the presence of a catalytic amount of RuHCl(CO)(PPh3)(3). On the other hand, (Z)-selective reactions are successfully conducted in 91-99% selectivity by using Ru(SiMe2Ph)Cl(CO)(PPr'(3))(2) as the catalyst. All reactions readily proceed at room temperature in high yields. (E)- and (Z)-styrylsilanes having a SiMe2[C6H3-3,5-(CF3)(2)] group serve as good cross-coupling reagents with p-iodotoluene in the presence of tetrabutylammonium. fluoride and [Pd(eta(3)-al-lyl)Cl](2) catalyst. (C) 2002 Elsevier Science B.V. All rights reserved.
• Stereoselective Synthesis of <i>cis</i>- and <i>trans</i>-Oligo(phenylenevinylene)s via Palladium-Catalyzed Cross-Coupling Reactions
  作者：Hiroyuki Katayama、Masato Nagao、Fumiyuki Ozawa、Masashi Ikegami、Tatsuo Arai

  DOI：10.1021/jo052602c

  日期：2006.3.31

  cis-Oligo(phenylenevinylene)s (OPVs) are synthesized by Suzuki−Miyaura coupling of arylboronic acids with (Z)-bromoalkenes in over 96% geometrical purity. On the other hand, trans-oligo(phenylenevinylene)s can be synthesized by Hiyama coupling of aryl iodide with (E)-alkenylsilanes in almost perfect purities. Effect of π-conjugation chain length on photoisomerization behavior of OPVs is described.

  顺式-低聚（亚苯基亚乙烯基）（OPV）是通过芳族硼酸与（Z）-溴代烯烃的Suzuki-Miyaura偶联以96％以上的几何纯度合成的。另一方面，反式-低聚（亚苯基亚乙烯基）可以通过芳基碘化物与（E）-烯基硅烷的Hiyama偶联以几乎完美的纯度来合成。描述了π共轭链长度对OPVs光异构化行为的影响。