A dual-purpose copper(I) coordination polymer for the construction of self-driven photoinduced C-H arylation systems
The simultaneous exploitation of dual or multiple physical and chemical properties of a material is a promising strategy for developing high-tech intelligent complex systems. In this study, a copper(I) coordination polymer (CuI-CP, 2) was synthesized and utilized as a dual-purpose material to constr...
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Veröffentlicht in: | Inorganic chemistry frontiers 2024-11 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The simultaneous exploitation of dual or multiple physical and chemical properties of a material is a promising strategy for developing high-tech intelligent complex systems. In this study, a copper(I) coordination polymer (CuI-CP, 2) was synthesized and utilized as a dual-purpose material to construct a self-powered photocatalytic system capable of significantly improving the power generation capabilities of triboelectric generators (TEGs) as a triboelectric layer and efficiently catalyzing the C-H arylation reaction as a photocatalyst. Compound 2 was achieved via a solvothermal method in the presence of ammonia and ethylenediamine. In contrast, only mixed-valence cooper salts ([CuII(H2O)5][CuI3(CN)5]·H2O, 1) were obtained without ammonia and ethylenediamine. Comparative analysis revealed that TEG based on 2 (2-TEG) showcased superior output performance compared to 1-TEG owing to the exceptional electron-donating ability of 2. Furthermore, under light-emitting diodes (LEDs) irradiation powered by 2-TEG, 2 demonstrated remarkable catalytic activity and selectivity in the photoinduced C-H arylation of benzothiazole, far exceeding the performance of 1. This research highlights the potential of bifunctional material 2 with a distinctive structure, renowned for its outstanding energy harvesting and conversion capabilities as well as excellent photocatalytic performance, thereby facilitating the design objectives of multitasking in self-driven complex systems. |
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ISSN: | 2052-1553 2052-1553 |
DOI: | 10.1039/D4QI02381A |