Xu Youzhi, Wang Bingzhe, Kaur Ramandeep, Minameyer Martin B, Bothe Michael, Drewello Thomas, Guldi Dirk M, von Delius Max
Institute of Organic Chemistry and Advanced Materials, University of Ulm, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Department of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials, Friedrich-Alexander University Erlangen-Nürnberg, Egerlandstrasse 3, 91058, Erlangen, Germany.
Angew Chem Int Ed Engl. 2018 Sep 3;57(36):11549-11553. doi: 10.1002/anie.201802443. Epub 2018 Aug 6.
Efficient photoinduced electron transfer was observed across a [10]cycloparaphenylene ([10]CPP) moiety that serves as a rigid non-covalent bridge between a zinc porphyrin and a range of fullerenes. The preparation of iodo-[10]CPP is the key to the synthesis of a porphyrin-[10]CPP conjugate, which binds C , C , (C ) , and other fullerenes (K >10 m ). Fluorescence and pump-probe spectroscopy revealed intramolecular energy transfer between CPP and porphyrin and also efficient charge separation between porphyrin and fullerenes, affording up to 0.5 μs lifetime charge-separated states. The advantage of this approach towards electron donor-acceptor dyads is evident in the case of dumbbell-shaped (C ) , which gave intricate charge-transfer behavior in 1:1 and 2:1 complexes. These results suggest that [10]CPP and its cross-coupled derivatives could act as supramolecular mediators of charge transport in organic electronic devices.
在一个[10]环对亚苯基([10]CPP)部分观察到了高效的光致电子转移,该部分作为锌卟啉与一系列富勒烯之间的刚性非共价桥。碘代-[10]CPP的制备是卟啉-[10]CPP共轭物合成的关键,该共轭物能结合C、C、(C)以及其他富勒烯(K>10 m)。荧光和泵浦-探测光谱揭示了CPP与卟啉之间的分子内能量转移以及卟啉与富勒烯之间的高效电荷分离,产生了长达0.5微秒寿命的电荷分离态。这种构建电子供体-受体二元体系的方法的优势在哑铃状(C)的情况下很明显,其在1:1和2:1配合物中表现出复杂的电荷转移行为。这些结果表明,[10]CPP及其交叉偶联衍生物可作为有机电子器件中电荷传输的超分子介质。