Indexed by:Journal Papers

Date of Publication:2015-07-02

Journal:JOURNAL OF PHYSICAL CHEMISTRY A

Included Journals:SCIE、EI、PubMed、Scopus

Volume:119

Issue:26

Page Number:6791-6806

ISSN No.:1089-5639

Abstract:2,6-Diiodobodipy-styrylbodipy dyads were prepared to study the competing intersystem crossing (ISC) and the fluorescence-resonance-energy-transfer (FRET), and its effect on the photophysical property of the dyads. In the dyads, 2,6-diiodobodipy moiety was used as singlet energy donor and the spin converter for triplet state formation, whereas the styrylbodipy was used as singlet and triplet energy acceptors, thus the competition between the ISC and FRET processes is established. The photophysical properties were studied with steady-state UV-vis absorption and fluorescence spectroscopy, electrochemical characterization, and femto/nano-second time-resolved transient absorption spectroscopies. FRET was confirmed with steady state fluorescence quenching and fluorescence excitation spectra and ultrafast transient absorption spectroscopy (k(FRET) = 5.0 X 10(10) s(-1)). The singlet oxygen quantum yield (Phi(Delta) = 0.19) of the dyad was reduced as compared with that of the reference spin converter (2,6-diiodobodipy, Phi(Delta) = 0.85), thus the ISC was substantially inhibited by FRET. Photoinduced intramolecular electron transfer (ET) was studid by electrochemical data and fluorescence quenching. Intermolecular triplet energy transfer was studied with nanosecond transient absorption spectroscopy as an efficient (Phi(TTET) = 92%) and fast process (k(TTET) = 5.2 x 10(4) s(-1)). These results are useful for designing organic triplet photosensitizers and for the study of the photophysical properties.