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硼二吡咯-苝酰亚胺紧密二元体和三元体中的高效自旋轨道电荷转移系间窜越及慢速分子内三重态-三重态能量转移

Efficient Spin-Orbit Charge-Transfer Intersystem Crossing and Slow Intramolecular Triplet-Triplet Energy Transfer in Bodipy-Perylenebisimide Compact Dyads and Triads.

作者信息

Chen Xi, Rehmat Noreen, Kurganskii Ivan V, Maity Partha, Elmali Ayhan, Zhao Jianzhang, Karatay Ahmet, Mohammed Omar F, Fedin Matvey V

机构信息

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.

International Tomography Center, SB RAS, and, Novosibirsk State University, 630090, Novosibirsk, Russia.

出版信息

Chemistry. 2023 Nov 2;29(61):e202302137. doi: 10.1002/chem.202302137. Epub 2023 Sep 25.

Abstract

Bodipy (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 (Φ =85 %) was observed than the bay-substituted derivative BDP-PBI-1 (Φ =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 PBI* (179.8 μs) state is populated. Nanosecond transient absorption spectra of BDP-PBI-3 show that the CR gives upper triplet excited state ( BDP*) and subsequently, via a slow intramolecular triplet energy transfer (14.5 μs), the PBI* 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 /T states mixing.

摘要

制备了硼二吡咯(Bodipy,BDP)-苝二酰亚胺(PBI)供体-受体二元/三元体系,用于研究自旋轨道电荷转移系间窜越(SOCT-ISC)。对于在PBI的酰亚胺位置连接BDP的BDP-PBI-3,观察到其单线态氧量子产率(Φ = 85%)高于湾位取代衍生物BDP-PBI-1(Φ = 30%)。飞秒瞬态吸收光谱表明,BDP-PBI-3中存在缓慢的Förster共振能量转移(FRET;40.4 ps)和电荷分离(CS;1.55 ns),而对于BDP-PBI-1,CS耗时2.8 ps。对于三元体系BDP-PBI-2,观察到超快FRET(149 fs)和CS(4.7 ps)过程,随后的电荷复合(CR)耗时5.8 ns,且形成了长寿命的PBI*(179.8 μs)态。BDP-PBI-3的纳秒瞬态吸收光谱表明,CR产生了上三重激发态(BDP*),随后通过缓慢的分子内三重态能量转移(14.5 μs),最终形成了PBI*态,这表明上三重态参与了SOCT-ISC。时间分辨电子顺磁共振光谱表明,自由基对系间窜越(RP ISC)和SOCT-ISC都对系间窜越有贡献。由于S-T/T态混合,通过RP ISC机制形成的三重态观察到了罕见的(e, e, e, e, e, e)电子自旋极化。

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