Abstract

In the scientific race to build up photoactive electron donor‐acceptor systems with increasing efficiencies, little is known about the interplay of their building blocks when integrated into supramolecular nanoscale arrays, particularly in aqueous environments. Here, we describe an aqueous donor‐acceptor ensemble whose emergence as a nanoscale material renders it remarkably stable and efficient. We have focused on a tetracationic zinc phthalocyanine (ZnPc) featuring pyrenes, which shows an unprecedented mode of aggregation, driven by subtle cooperation between electrostatic and π–π interactions. Our studies demonstrate monocrystalline growth in solution and a symmetry‐breaking intermolecular charge transfer between adjacent ZnPcs upon photoexcitation. Immobilizing a negatively charged fullerene (C60) as electron acceptor onto the monocrystalline ZnPc assemblies was found to enhance the overall stability, and to suppress the energy‐wasting charge recombination found in the absence of C60. Overall, the resulting artificial photosynthetic model system exhibits a high degree of preorganization, which facilitates efficient charge separation and subsequent charge transport.

Highlights

  • Natural photosynthesis is a key, highly sophisticated biological process that allows the conversion of light into chemical energy.[1]

  • zinc phthalocyanine (ZnPc) 7 was obtained by cyclotetramerization of phthalonitrile 6 in the presence of anhydrous zinc acetate as a metal salt template, and refluxing 2-dimethylaminoethanol as solvent

  • We have described a tetracationic ZnPc featuring pyrenes, which shows an unprecedented mode of aggregation in aqueous medium

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Summary

Introduction

Natural photosynthesis is a key, highly sophisticated biological process that allows the conversion of light into chemical energy.[1]. A symmetry-breaking charge separation occurs in the aggregates of 1, as a consequence of the greatly facilitated transfer of electrons and holes between neighboring ZnPc molecules. When these aggregates interact with either tetra- or octaanionic water-soluble fullerenes (3 or 4), the resulting unidirectional charge separation yields an appreciably longer-lived charge-separated state

Results and Discussion
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