| Photochromic fulgides and spirooxazines: mechanism and substituent effect on photoreactions |
| |
| 引用本文： | 樊美公,明阳福,于联合,张新宇,孟宪娟,梁永超,杨茁. Photochromic fulgides and spirooxazines: mechanism and substituent effect on photoreactions[J]. 中国科学B辑(英文版), 1996, 0(2) |
| |
| 作者姓名： | 樊美公 明阳福 于联合 张新宇 孟宪娟 梁永超 杨茁 |
| |
| 作者单位： | Institute of Photographic Chemistry，Chinese Academy of Sciences，Beijing 100101，China，Institute of Photographic Chemistry，Chinese Academy of Sciences，Beijing 100101，China，Institute of Photographic Chemistry，Chinese Academy of Sciences，Beijing 100101，China，Institute of Photographic Chemistry，Chinese Academy of Sciences，Beijing 100101，China，Institute of Photographic Chemistry，Chinese Academy of Sciences，Beijing 100101，China，Institute of Photographic Chemistry，Chinese Academy of Sciences，Beijing 100101，China，Institute of Photographic Chemistry，Chinese Academy of Sciences，Beijing 100101，China |
| |
| 基金项目： | Project supported by the National Natural Science Foundation of China |
| |
| 摘 要： | Molecular design, synthesis and photochromic properties of spirooxazines and fulgides are described. In the case of fulgides, the change of the substituents may lead to different photochromic properties and different photoreactions of the kind of compounds. In photochromic process of pyrryl-substituted fulgides, the excited singlet state is the mam species, but the excited triplet state is also involved. However, no excited triplet state has been observed in cyclization of aryl-substituted fulgides. In the case of spirooxazines, the substituents at 2'-position have great effect on the formation of photoproduct and on the mechanism of photoreaction. The increase of steric hindrance of the 2'-position substituent gives rise to the decrease of the quantum yield for the formation of photochromic merocyanine (PMC) and the increase of the relative quantum yield for the charge separated twist intermediate (CT).
|
Photochromic fulgides and spirooxazines: mechanism and substituent effect on photoreactions |
| |
| FAN Meigong MING Yangfu,YU LianheZHANG Xinyu MENG XianjuanLIANG Yongchao and YANG Zhuo. Photochromic fulgides and spirooxazines: mechanism and substituent effect on photoreactions[J]. Science in China(Chemistry), 1996, 0(2) |
| |
| Authors: | FAN Meigong MING Yangfu YU LianheZHANG Xinyu MENG XianjuanLIANG Yongchao YANG Zhuo |
| |
| Abstract: | Molecular design, synthesis and photochromic properties of spirooxazines and fulgides are described. In the case of fulgides, the change of the substituents may lead to different photochromic properties and different photoreactions of the kind of compounds. In photochromic process of pyrryl-substituted fulgides, the excited singlet state is the mam species, but the excited triplet state is also involved. However, no excited triplet state has been observed in cyclization of aryl-substituted fulgides. In the case of spirooxazines, the substituents at 2'-position have great effect on the formation of photoproduct and on the mechanism of photoreaction. The increase of steric hindrance of the 2'-position substituent gives rise to the decrease of the quantum yield for the formation of photochromic merocyanine (PMC) and the increase of the relative quantum yield for the charge separated twist intermediate (CT). |
| |
| Keywords: | photochromism spirooxazines fulgides photoreaction. |
| 本文献已被 CNKI 等数据库收录！ |
