5-[4-[4-(2,5-Dimethylphenyl)-2,5-dimethoxyphenyl]-2,3,5,6-tetramethoxyphenyl]-2-pyridin-2-ylpyridine | 1338236-88-6

• 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: 5-[4-[4-(2,5-Dimethylphenyl)-2,5-dimethoxyphenyl]-2,3,5,6-tetramethoxyphenyl]-2-pyridin-2-ylpyridine
• 英文别名: 5-[4-[4-(2,5-dimethylphenyl)-2,5-dimethoxyphenyl]-2,3,5,6-tetramethoxyphenyl]-2-pyridin-2-ylpyridine
• CAS: 1338236-88-6
• 化学式: C₃₆H₃₆N₂O₆
• 分子量: 592.692
• InChiKey: CGVISVZYRJEZJC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.9
• 重原子数：
  44
• 可旋转键数：
  10
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  81.2
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  顺-双(2,2'-二吡啶基)二氯化钌(II)二水合物 、 5-[4-[4-(2,5-Dimethylphenyl)-2,5-dimethoxyphenyl]-2,3,5,6-tetramethoxyphenyl]-2-pyridin-2-ylpyridine 以 not given 为溶剂， 生成
  参考文献：
  名称：

  Hole Tunneling and Hopping in a Ru(bpy)₃²⁺-Phenothiazine Dyad with a Bridge Derived from oligo-p-Phenylene

  摘要：

  A molecular dyad was synthesized in which a Ru(bpy)(3)(2+) (bpy = 2,2'-bipyridine) photosensitizer and a phenothiazine redox partner are bridged by a sequence of tetramethoxybenzene, p-dimethoxybenzene, and p-xylene units. Hole transfer from the oxidized metal complex to the phenothiazine was triggered using a flash-quench technique and investigated by transient absorption spectroscopy. Optical spectroscopic and electrochemical experiments performed on a suitable reference molecule in addition to the above-mentioned dyad lead to the conclusion that hole transfer from Ru(bpy)(3)(3+) to phenothiazine proceeds through a sequence of hopping and tunneling steps: Initial hole hopping from Ru(bpy)(3)(3+) to the easily oxidizable tetramethoxybenzene unit is followed by tunneling through the barrier imposed by the p-dimethoxybenzene and p-xylene spacers. The overall charge transfer proceeds with a time constant of 41 ns, which compares favorably to a time constant of 1835 ns associated with equidistant hole tunneling between the same donor acceptor couple bridged by three identical p-xylene units. The combined hopping/tunneling sequence thus leads to an acceleration of hole transfer by roughly a factor of 50 when compared to a pure tunneling mechanism.

  DOI：

  10.1021/ic201446x
• 作为产物：
  描述：

  2,5-dimethoxy-4-(trimethylsilyl)phenylboronic acid 在 四(三苯基膦)钯 、 三叔丁基膦 、 一氯化碘 、 sodium carbonate 、 caesium carbonate 、 bis(dibenzylideneacetone)-palladium⁽⁰⁾ 作用下， 以 1,4-二氧六环 、 二氯甲烷 、 水 、 甲苯 、 乙腈 为溶剂， 生成 5-[4-[4-(2,5-Dimethylphenyl)-2,5-dimethoxyphenyl]-2,3,5,6-tetramethoxyphenyl]-2-pyridin-2-ylpyridine
  参考文献：
  名称：

  Hole Tunneling and Hopping in a Ru(bpy)₃²⁺-Phenothiazine Dyad with a Bridge Derived from oligo-p-Phenylene

  摘要：

  A molecular dyad was synthesized in which a Ru(bpy)(3)(2+) (bpy = 2,2'-bipyridine) photosensitizer and a phenothiazine redox partner are bridged by a sequence of tetramethoxybenzene, p-dimethoxybenzene, and p-xylene units. Hole transfer from the oxidized metal complex to the phenothiazine was triggered using a flash-quench technique and investigated by transient absorption spectroscopy. Optical spectroscopic and electrochemical experiments performed on a suitable reference molecule in addition to the above-mentioned dyad lead to the conclusion that hole transfer from Ru(bpy)(3)(3+) to phenothiazine proceeds through a sequence of hopping and tunneling steps: Initial hole hopping from Ru(bpy)(3)(3+) to the easily oxidizable tetramethoxybenzene unit is followed by tunneling through the barrier imposed by the p-dimethoxybenzene and p-xylene spacers. The overall charge transfer proceeds with a time constant of 41 ns, which compares favorably to a time constant of 1835 ns associated with equidistant hole tunneling between the same donor acceptor couple bridged by three identical p-xylene units. The combined hopping/tunneling sequence thus leads to an acceleration of hole transfer by roughly a factor of 50 when compared to a pure tunneling mechanism.

  DOI：

  10.1021/ic201446x

文献信息

• Hole Tunneling and Hopping in a Ru(bpy)₃²⁺-Phenothiazine Dyad with a Bridge Derived from oligo-<i>p</i>-Phenylene
  作者：Mathieu E. Walther、Oliver S. Wenger

  DOI：10.1021/ic201446x

  日期：2011.11.7

  A molecular dyad was synthesized in which a Ru(bpy)(3)(2+) (bpy = 2,2'-bipyridine) photosensitizer and a phenothiazine redox partner are bridged by a sequence of tetramethoxybenzene, p-dimethoxybenzene, and p-xylene units. Hole transfer from the oxidized metal complex to the phenothiazine was triggered using a flash-quench technique and investigated by transient absorption spectroscopy. Optical spectroscopic and electrochemical experiments performed on a suitable reference molecule in addition to the above-mentioned dyad lead to the conclusion that hole transfer from Ru(bpy)(3)(3+) to phenothiazine proceeds through a sequence of hopping and tunneling steps: Initial hole hopping from Ru(bpy)(3)(3+) to the easily oxidizable tetramethoxybenzene unit is followed by tunneling through the barrier imposed by the p-dimethoxybenzene and p-xylene spacers. The overall charge transfer proceeds with a time constant of 41 ns, which compares favorably to a time constant of 1835 ns associated with equidistant hole tunneling between the same donor acceptor couple bridged by three identical p-xylene units. The combined hopping/tunneling sequence thus leads to an acceleration of hole transfer by roughly a factor of 50 when compared to a pure tunneling mechanism.