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首页> 外文期刊>Physical chemistry chemical physics: PCCP >Sequential energy and charge transfer processes in mixed host-guest complexes of subphthalocyanine, porphyrin and phthalocyanine chromophores
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Sequential energy and charge transfer processes in mixed host-guest complexes of subphthalocyanine, porphyrin and phthalocyanine chromophores

机译:亚酞菁,卟啉和酞菁生色团的混合主体-客体复合物中的顺序能量和电荷转移过程

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摘要

Porphyrins, phthalocyanines and subphthalocyanines are three attractive classes of chromophores with intriguing properties making them suitable for the design of artificial photosynthetic systems. The assembly of these components by a supramolecular approach is of particular interest as it provides a facile means to build multi-chromophoric arrays with various architectures and tuneable photophysical properties. In this paper, we show the formation of mixed host-guest supramolecular complexes that consist of a P-cyclodextrin-conjugated subphthalocyanine, a tetrasulfonated porphyrin and a series of silicon(IV) phthalocyanines substituted axially with two β-cyclodextrins via different spacers. We found that the three components form supramolecular complexes held by host-guest interactions in aqueous solution. Upon excitation of the subphthalocyanine part of the complex, the excitation energy is delivered to the phthalocyanine unit via excitation energy transfer and the porphyrin chromophore acts as an energy transfer bridge enabling this process. It was shown that photo-induced charge transfer also takes place. A sequential electron transfer process from the porphyrin unit to the phthalocyanine moiety and subsequently from the subphthalocyanine moiety to the porphyrin unit takes place, and the probability of this process is controlled by the linker between β-cyclodextrin and phthalocyanine. The lifetime of the charge-separated state was found to be 1.7 ns by transient absorption spectroscopy.
机译:卟啉,酞菁和亚酞菁是具有吸引力特性的三类发色团,使其适合用于人工光合作用系统的设计。通过超分子方法组装这些组分是特别令人感兴趣的,因为它提供了构建具有各种结构和可调节的光物理性质的多发色性阵列的简便方法。在本文中,我们显示了由P-环糊精共轭的亚酞菁,四磺化卟啉和一系列通过不同间隔基轴向被两个β-环糊精轴向取代的硅(IV)酞菁组成的混合主体-客体超分子复合物的形成。我们发现,这三种成分形成由宿主-客体相互作用在水溶液中保持的超分子复合物。在激发配合物的亚酞菁部分时,激发能量通过激发能传递被传递到酞菁单元,并且卟啉生色团充当实现该过程的能量传递桥。结果表明,光诱导的电荷转移也发生了。从卟啉单元到酞菁部分,然后从亚酞菁部分到卟啉单元的顺序电子转移过程发生,并且该过程的可能性由β-环糊精和酞菁之间的连接基控制。通过瞬态吸收光谱法发现电荷分离状态的寿命为1.7ns。

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