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Light triggers molecular shuttling in rotaxanes: control over proximity and charge recombination

机译:光触发轮烷中的分子穿梭:控制接近度和电荷重组

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摘要

We present the synthesis of novel rotaxanes based on mechanically interlocked porphyrins and fullerene and their advanced investigations by means of photophysical measurements. To this end, a fullerene-capped dumbbell-type axle containing a central triazole was threaded through strapped (metallo)porphyrins—either a free-base or a zinc porphyrin. Femtosecond-resolved transient absorption measurements revealed charge-separation between the porphyrin and fullerene upon light excitation. Solvent polarity and solvent coordination effects induced molecular motion of the rotaxanes upon charge separation and enabled, for the first time, subtle control over the charge recombination by enabling and controlling the directionality of shuttling.
机译:我们目前基于机械互锁的卟啉和富勒烯的新型轮烷的合成及其通过光物理测量的高级研究。为此,将含有中心三唑的富勒烯封盖的哑铃型轴穿过带束缚的(金属)卟啉-游离碱或卟啉锌。飞秒分辨的瞬态吸收测量表明,光激发后卟啉和富勒烯之间发生电荷分离。溶剂极性和溶剂配位效应在电荷分离时引起轮烷的分子运动,并且通过启用和控制穿梭的方向性,首次实现了对电荷重组的微妙控制。

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