π-Topology and ultrafast excited-state dynamics of remarkably photochemically stabilized pentacene derivatives with radical substituents

被引:7
|
作者
Minami, Nishiki [1 ]
Yoshida, Kohei [1 ]
Maeguchi, Keijiro [1 ]
Kato, Ken [1 ]
Shimizu, Akihiro [1 ]
Kashima, Genta [1 ]
Fujiwara, Masazumi [1 ]
Uragami, Chiasa [2 ]
Hashimoto, Hideki [2 ]
Teki, Yoshio [1 ]
机构
[1] Osaka City Univ, Grad Sch Sci, Div Mol Mat Sci, Dept Chem,Sumiyoshi Ku, 3-3-138 Sugimoto, Osaka 5588585, Japan
[2] Kwansei Gakuin Univ, Grad Sch Sci & Technol, Dept Appl Chem Environm, Sanda, Hyogo 6691337, Japan
基金
日本学术振兴会;
关键词
SPIN ALIGNMENT; ACENES; TRIPLET; SINGLET;
D O I
10.1039/d2cp00683a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Pentacene derivatives with both pi-radical- and TIPS-substituents (1m and 1p) were synthesized and their photochemical properties and excited-state dynamics were evaluated. The pentacene-radical-linked systems 1m (1p) showed a remarkable improvement in photochemical stability, which was 187 (139) times higher than that of 6,13-bis(triisopropylsilylethynyl)pentacene. Transient absorption spectroscopy showed that this remarkable photostabilization is due to the ultrafast intersystem crossing induced by effective pi-conjugation between the radical substituent and pentacene moiety. The relationship between pi-topology and the photochemical stability is also discussed based on the excited-state dynamics.
引用
收藏
页码:13514 / 13518
页数:6
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