Affiliation:
1. State Key Laboratory of Fine Chemicals Frontiers Science Center for Smart Materials School of Chemical Engineering Dalian University of Technology Dalian 116024 P.R. China
2. International Tomography Center SB RAS and Novosibirsk State University 630090 Novosibirsk Russia
3. Division of Physical Sciences and Engineering King Abdullah University of Science and Technology (KAUST) Thuwal 23955-6900 Kingdom of Saudi Arabia
4. Department of Engineering Physics Faculty of Engineering Ankara University 06100 Beşevler Ankara Türkiye
Abstract
AbstractBodipy (BDP)‐perylenebisimide (PBI) donor–acceptor dyads/triad were prepared to study the spin–orbit charge‐transfer intersystem crossing (SOCT‐ISC). For BDP‐PBI‐3, in which BDP was attached at the imide position of PBI, higher singlet oxygen quantum yield (ΦΔ=85 %) was observed than the bay‐substituted derivative BDP‐PBI‐1 (ΦΔ=30 %). Femtosecond transient absorption spectra indicate slow Förster resonance energy transfer (FRET; 40.4 ps) and charge separation (CS; 1.55 ns) in BDP‐PBI‐3, while for BDP‐PBI‐1, CS takes 2.8 ps. For triad BDP‐PBI‐2, ultrafast FRET (149 fs) and CS (4.7 ps) process were observed, the subsequent charge recombination (CR) takes 5.8 ns and long‐lived 3PBI* (179.8 μs) state is populated. Nanosecond transient absorption spectra of BDP‐PBI‐3 show that the CR gives upper triplet excited state (3BDP*) and subsequently, via a slow intramolecular triplet energy transfer (14.5 μs), the 3PBI* state is finally populated, indicating that upper triplet state is involved in SOCT‐ISC. Time‐resolved electron paramagnetic resonance spectroscopy revealed that both radical pair ISC (RP ISC) and SOCT‐ISC contribute to the ISC. A rare electron spin polarization of (e, e, e, e, e, e) was observed for the triplet state formed via the RP ISC mechanism, due to the S−T+1/T0 states mixing.
Funder
National Natural Science Foundation of China
Dalian University of Technology
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献