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萘二酰亚胺-蒽紧密供体-受体二元体系中的电荷分离/复合、系间窜越及异常缓慢的分子内三重态-三重态能量转移

Charge Separation/Recombination, Intersystem Crossing, and Unusually Slow Intramolecular Triplet-Triplet Energy Transfer in Naphthalenediimide-Anthracene Compact Energy Donor-Acceptor Dyads.

作者信息

Chen Xi, Sukhanov Andrey A, Taddei Maria, Dick Bernhard, Zhao Jianzhang, Voronkova Violeta K, Di Donato Mariangela

机构信息

State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials Oriented Chemical Engineering, School of Chemical Engineering, Dalian University of Technology, E-208 West Campus, 2 Ling Gong Road, Dalian 116024, P. R. China.

Zavoisky Physical-Technical Institute, FRC Kazan Scientific Center of RAS, Kazan 420029, Russia.

出版信息

J Phys Chem Lett. 2022 Sep 22;13(37):8740-8748. doi: 10.1021/acs.jpclett.2c02118. Epub 2022 Sep 13.

Abstract

Three anthracene (An)-naphthalenediimide (NDI) compact electron donor-acceptor dyads were prepared. Femtosecond transient absorption (fs-TA) spectra show fast charge separation (ca. 0.9-1.7 ps) and relatively slow charge recombination (ca. 8-565 ps) upon photoexcitation; moreover, the An state was observed for , whereas the final state is NDI for both and , which have an intervening phenyl linker between the An and NDI units. Nanosecond transient absorption (ns-TA) spectra indicate that the lowest triplet state of all the dyads is An, with triplet lifetimes of 139-354 μs. An unusually slow intramolecular triplet-triplet energy transfer (TTET) was observed for and (32-85 ns). Time-resolved electron paramagnetic resonance (TREPR) spectroscopy confirms that the intersystem crossing (ISC) mechanism is spin orbit charge transfer ISC (SOCT-ISC) for all the dyads; for , only the An state was observed, while for the other two dyads, both NDI and An states were observed, with their relative population changing with increasing delay time, which supports TTET.

摘要

制备了三种蒽(An)-萘二亚胺(NDI)紧密电子供体-受体二元化合物。飞秒瞬态吸收(fs-TA)光谱表明,光激发后电荷快速分离(约0.9 - 1.7皮秒)且电荷复合相对较慢(约8 - 565皮秒);此外,对于[具体情况未给出]观察到了An态,而对于[具体情况未给出]和[具体情况未给出],最终态均为NDI态,它们在An和NDI单元之间有一个中间苯基连接基团。纳秒瞬态吸收(ns-TA)光谱表明,所有二元化合物的最低三重态均为An,三重态寿命为139 - 354微秒。对于[具体情况未给出]和[具体情况未给出]观察到了异常缓慢的分子内三重态-三重态能量转移(TTET)(32 - 85纳秒)。时间分辨电子顺磁共振(TREPR)光谱证实,所有二元化合物的系间窜越(ISC)机制均为自旋轨道电荷转移ISC(SOCT-ISC);对于[具体情况未给出],仅观察到了An态,而对于其他两种二元化合物,同时观察到了NDI态和An态,它们的相对丰度随延迟时间增加而变化,这支持了TTET。

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