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基于三重态-三重态湮灭上转换的单发色团(BODIPY)衍生的长寿命三重态激发态有机三重态敏化剂库。

Organic triplet sensitizer library derived from a single chromophore (BODIPY) with long-lived triplet excited state for triplet-triplet annihilation based upconversion.

机构信息

State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, E-208 Western Campus, 2 Ling-Gong Rd., Dalian 116024, China.

出版信息

J Org Chem. 2011 Sep 2;76(17):7056-64. doi: 10.1021/jo200990y. Epub 2011 Aug 9.

DOI:10.1021/jo200990y
PMID:21786760
Abstract

Triplet-triplet annihilation (TTA) based upconversions are attractive as a result of their readily tunable excitation/emission wavelength, low excitation power density, and high upconversion quantum yield. For TTA upconversion, triplet sensitizers and acceptors are combined to harvest the irradiation energy and to acquire emission at higher energy through triplet-triplet energy transfer (TTET) and TTA processes. Currently the triplet sensitizers are limited to the phosphorescent transition metal complexes, for which the tuning of UV-vis absorption and T(1) excited state energy level is difficult. Herein for the first time we proposed a library of organic triplet sensitizers based on a single chromophore of boron-dipyrromethene (BODIPY). The organic sensitizers show intense UV-vis absorptions at 510-629 nm (ε up to 180,000 M(-1) cm(-1)). Long-lived triplet excited state (τ(T) up to 66.3 μs) is populated upon excitation of the sensitizers, proved by nanosecond time-resolved transient difference absorption spectra and DFT calculations. With perylene or 1-chloro-9,10-bis(phenylethynyl)anthracene (1CBPEA) as the triplet acceptors, significant upconversion (Φ(UC) up to 6.1%) was observed for solution samples and polymer films, and the anti-Stokes shift was up to 0.56 eV. Our results pave the way for the design of organic triplet sensitizers and their applications in photovoltaics and upconversions, etc.

摘要

三重态-三重态湮灭(TTA)基上转换因其可调谐的激发/发射波长、低激发功率密度和高上转换量子产率而备受关注。对于 TTA 上转换,三重态敏化剂和受体结合在一起,通过三重态-三重态能量转移(TTET)和 TTA 过程来收集辐照能量,并获得更高能量的发射。目前,三重态敏化剂仅限于磷光过渡金属配合物,对于这些配合物,很难调节 UV-vis 吸收和 T(1)激发态能级。在此,我们首次提出了基于硼二吡咯甲川(BODIPY)单发色团的有机三重态敏化剂库。有机敏化剂在 510-629nm 处表现出强烈的紫外可见吸收(ε高达 180,000 M(-1) cm(-1))。通过纳秒时间分辨瞬态差分吸收光谱和 DFT 计算证明,敏化剂激发后会产生长寿命的三重态激发态(τ(T)高达 66.3μs)。以苝或 1-氯-9,10-双(苯乙炔基)蒽(1CBPEA)作为三重态受体,在溶液样品和聚合物薄膜中观察到显著的上转换(Φ(UC)高达 6.1%),反斯托克斯位移高达 0.56eV。我们的结果为设计有机三重态敏化剂及其在光伏和上转换等方面的应用铺平了道路。

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