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Visible-Light-Responsive Self-Assembled Complexes: Improved Photoswitching Properties by Metal Ion Coordination.


ABSTRACT: A photoswitchable ligand based on azobenzene is self-assembled with palladium(II) ions to form a [Pd2 (E-L)4 ]4+ cage. Irradiation with 470 nm light results in the near-quantitative switching to a monomeric species [Pd(Z-L)2 ]2+ , which can be reversed by irradiation with 405 nm light, or heat. The photoswitching selectivity towards the metastable isomer is significantly improved upon self-assembly, and the thermal half-life is extended from 40 days to 850 days, a promising approach for tuning photoswitching properties.

SUBMITTER: DiNardi RG 

PROVIDER: S-EPMC9541570 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature

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Visible-Light-Responsive Self-Assembled Complexes: Improved Photoswitching Properties by Metal Ion Coordination.

DiNardi Ray G RG   Douglas Anna O AO   Tian Ruoming R   Price Jason R JR   Tajik Mohammad M   Donald William A WA   Beves Jonathon E JE  

Angewandte Chemie (International ed. in English) 20220816 38


A photoswitchable ligand based on azobenzene is self-assembled with palladium(II) ions to form a [Pd<sub>2</sub> (E-L)<sub>4</sub> ]<sup>4+</sup> cage. Irradiation with 470 nm light results in the near-quantitative switching to a monomeric species [Pd(Z-L)<sub>2</sub> ]<sup>2+</sup> , which can be reversed by irradiation with 405 nm light, or heat. The photoswitching selectivity towards the metastable isomer is significantly improved upon self-assembly, and the thermal half-life is extended from  ...[more]

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