4-(indol-1-yl)phthalonitrile | 1396398-46-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: 4-(indol-1-yl)phthalonitrile
• CAS: 1396398-46-1
• 化学式: C₁₆H₉N₃
• 分子量: 243.268
• InChiKey: NAOBKEJMUUHVEX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.37
• 重原子数：
  19.0
• 可旋转键数：
  1.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  52.51
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  4-(indol-1-yl)phthalonitrile 在 zinc diacetate 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 戊醇 为溶剂， 反应 4.0h， 以39%的产率得到
  参考文献：
  名称：

  Indole substituted zinc phthalocyanine: Improved photosensitizing ability and modified photooxidation mechanism

  摘要：

  The photophysical and photochemical processes within a novel photosensitizer (PS), zinc phthalocyanine (ZnPc) modified by indole units, were explored. The properties related to photodynamic therapy of tumor (PDT) were studied by time-resolved transient UV-vis absorption spectra, steady state and time-resolved fluorescence spectra, and chemical trapping of singlet oxygen by diphenylisobenzofuran (DPBF). Intramolecular photoinduced electron transfer (PET) within the conjugate from the indole subunits (donor A), to S-1 (excited singlet state) of ZnPc moiety (acceptor D), is featured by the significant decrease of fluorescence quantum yield and lifetime of ZnPc moiety, and the occurrence of transient absorption bands of ZnPc center dot- at 570 and 630 nm. The triplet state, on the other hand, was not quenched by indole units. The kinetics and thermodynamics of PET were analyzed quantitatively, and the quantum efficiency of PET is computed to be 38%, almost double of the emission efficiency (20%). The quantum efficiency of triplet (T-1) formation is 0.50 and the quantum yield of DPBF photooxidation is 0.72. Both are larger than the expected value of 0.32. The evolution of transient absorption spectra showed that the charge separation state (ZnPc center dot--indole(center dot+)) recombined to triplet state ZnPc(T-1)-indole, which is responsible for the high yield of T-1 formation. In the presence of oxygen, both T-1 and ZnPc center dot- were quenched efficiently, which forms singlet oxygen and superoxide anion, respectively. DPBF is therefore photo-oxidized by both singlet oxygen (Type II reaction, 46%) and superoxide anion radical (Type I reaction, 54%), which led to the high yield of photooxidation. This is in contrast to free ZnPc PS, in which only singlet oxygen is responsible for the photooxidation. The result suggests that the reaction mechanism is changed upon conjugation so that the importance of Type I reaction is greatly enhanced, and the indole-conjugated ZnPc is an even better PS than the free ZnPc. (C) 2011 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jphotochem.2011.10.008
• 作为产物：
  描述：

  吲哚 、 4-硝基邻苯二甲腈 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以43%的产率得到4-(indol-1-yl)phthalonitrile
  参考文献：
  名称：

  Indole substituted zinc phthalocyanine: Improved photosensitizing ability and modified photooxidation mechanism

  摘要：

  The photophysical and photochemical processes within a novel photosensitizer (PS), zinc phthalocyanine (ZnPc) modified by indole units, were explored. The properties related to photodynamic therapy of tumor (PDT) were studied by time-resolved transient UV-vis absorption spectra, steady state and time-resolved fluorescence spectra, and chemical trapping of singlet oxygen by diphenylisobenzofuran (DPBF). Intramolecular photoinduced electron transfer (PET) within the conjugate from the indole subunits (donor A), to S-1 (excited singlet state) of ZnPc moiety (acceptor D), is featured by the significant decrease of fluorescence quantum yield and lifetime of ZnPc moiety, and the occurrence of transient absorption bands of ZnPc center dot- at 570 and 630 nm. The triplet state, on the other hand, was not quenched by indole units. The kinetics and thermodynamics of PET were analyzed quantitatively, and the quantum efficiency of PET is computed to be 38%, almost double of the emission efficiency (20%). The quantum efficiency of triplet (T-1) formation is 0.50 and the quantum yield of DPBF photooxidation is 0.72. Both are larger than the expected value of 0.32. The evolution of transient absorption spectra showed that the charge separation state (ZnPc center dot--indole(center dot+)) recombined to triplet state ZnPc(T-1)-indole, which is responsible for the high yield of T-1 formation. In the presence of oxygen, both T-1 and ZnPc center dot- were quenched efficiently, which forms singlet oxygen and superoxide anion, respectively. DPBF is therefore photo-oxidized by both singlet oxygen (Type II reaction, 46%) and superoxide anion radical (Type I reaction, 54%), which led to the high yield of photooxidation. This is in contrast to free ZnPc PS, in which only singlet oxygen is responsible for the photooxidation. The result suggests that the reaction mechanism is changed upon conjugation so that the importance of Type I reaction is greatly enhanced, and the indole-conjugated ZnPc is an even better PS than the free ZnPc. (C) 2011 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jphotochem.2011.10.008