Indexed by:期刊论文

Date of Publication:2012-07-20

Journal:JOURNAL OF ORGANIC CHEMISTRY

Included Journals:SCIE、EI、PubMed、Scopus

Volume:77

Issue:14

Page Number:6166-6178

ISSN No.:0022-3263

Abstract:Bodipy derivatives containing excited state intramolecular proton transfer (ESIPT) chromophores 2-(2-hydroxyphenyl) benzothiazole and benzoxazole (HBT and HBO) subunits were prepared (7-1.0). The compounds show red-shifted UV-vis absorption (530-580 nm; epsilon up to 50000 M-1 cm(-1)) and emission compared to both HBT/HBO and Bodipy. The new chromophores show small Stokes shift (45 nm) and high fluorescence quantum yields (Phi(F) up to 36%), which are in stark contrast to HBT and HBO (Stokes shift up to 180 nm and Phi(F) as low as 0.6%). On the basis of steady state and time-resolved absorption spectroscopy, as well as DFT/TDDFT calculations, we propose that 7-9 do not undergo ESIPT upon photoexcitation. Interestingly, nanosecond time-resolved transient absorption spectroscopy demonstrated that Bodipy-localized triplet excited states were copulated for 7-10 upon photoexcitation; the lifetimes of the triplet excited states (tau(T)) are up to 195 mu s. DFT calculations confirm the transient absorptions are due to the triplet state. Different from the previous report, we demonstrated that population of the triplet excited states is not the result of ESIPT. The compounds were used as organic triplet photosensitizers for photooxidation of 1,5-dihydroxylnaphthalene. One of the compounds is more efficient than the conventional [Ir(ppy)(2)(phen)][PF6] triplet photosensitizer. Our result will be useful for design of new Bodipy derivatives, ESIPT compounds, and organic triplet photosensitize's, as well as for applications of these compounds in photovoltaics, photocatalysis and luminescent materials, etc.