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Synthesis of Perylene-3,4-mono(dicarboximide)−Fullerene C60 Dyads as New Light-Harvesting Systems

机译:作为新型光捕获系统的per -3,4-单(二羧酰亚胺) - 富勒烯C60二元体的合成

摘要

Fullerene C60−perylene-3,4-mono(dicarboximide) (C60−PMI) dyads 1−3 were synthesized in the search for new light-harvesting systems. The synthetic strategy to the PMI intermediate used a cross-coupling Suzuki reaction for the introduction of a formyl group in the ortho, meta, or para position. Subsequent 1,3-dipolar cycloaddition with C60 led to the target C60−PMI dyad. Cyclic voltammetry showed that the first one-electron reduction process unambiguously occurs onto the C60 moiety and the following two-electron process corresponds to the concomitant second reduction of C60 and the first reduction of PMI. A quasi-quantitative quenching of fluorescence was shown in dyads 1−3, and an intramolecular energy transfer was suggested to occur from the PMI to the fullerene moiety. These C60−PMI dyads constitute good candidates for future photovoltaic applications with expected well-defined roles for both partners, i.e., PMI acting as a light-harvesting antenna and C60 playing the role of the acceptor in the photoactive layer.
机译:为了寻找新的光收集系统,合成了富勒烯C60-per-3,4-单(二甲叉酰亚胺)(C60-PMI)二元组1-3。 PMI中间体的合成策略是使用交叉偶联的Suzuki反应在邻位,间位或对位引入甲酰基。随后的与C60的1,3-偶极环加成反应导致了目标C60-PMI二聚体。循环伏安法表明,第一个单电子还原过程明确地发生在C60部分上,随后的两个电子过程对应于C60的第二次还原和PMI的第一次还原。在二分体1-3中显示了荧光的准定量猝灭,并且提示分子内能量转移从PMI发生到富勒烯部分。这些C60-PMI双色构成了未来光伏应用的良好候选者,双方都有望获得明确定义的角色,即PMI充当光收集天线,而C60在光敏层中扮演受体的角色。

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