化学
光化学
吩噻嗪
双环分子
光诱导电荷分离
发色团
皮秒
辛烷值
纳秒
超快激光光谱学
立体化学
有机化学
光谱学
物理
催化作用
光学
药理学
人工光合作用
激光器
医学
光催化
量子力学
作者
Ayumu Karimata,Hidetoshi Kawauchi,Shuichi Suzuki,Masatoshi Kozaki,Noriaki Ikeda,Kazutoshi Keyaki,Koichi Nozaki,Kimio Akiyama,Keiji Okada
出处
期刊:Chemistry Letters
[The Chemical Society of Japan]
日期:2013-05-27
卷期号:42 (8): 794-796
被引量:20
摘要
Abstract Photoinduced charge separation of a phenothiazine–anthraquinone dyad 1 with a rigid bicyclo[2.2.2]octane spacer was investigated by means of picosecond and nanosecond transient absorption and time-resolved ESR spectroscopies. Irradiation of the anthraquinone chromophore in 1 produced the charge-separated (CS) state in THF. Time constants of the formation and the decay of the CS state were determined to be 1.3 ns and 1.0 µs, respectively. Time-resolved ESR showed spin-polarized all-emission signals due to the formation of the CS state via the triplet mechanism.
科研通智能强力驱动
Strongly Powered by AbleSci AI