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“Clicked” Hydrazone Photoswitches
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    “Clicked” Hydrazone Photoswitches
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    • Daniil Sosnin
      Daniil Sosnin
      6128 Burke Laboratory, Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755, United States
    • Mohammad Izadyar
      Mohammad Izadyar
      Fluorescence Research Group, Singapore University of Technology and Design, Singapore 487372, Singapore
    • Syed Ali Abbas Abedi
      Syed Ali Abbas Abedi
      Fluorescence Research Group, Singapore University of Technology and Design, Singapore 487372, Singapore
    • Xiaogang Liu
      Xiaogang Liu
      Fluorescence Research Group, Singapore University of Technology and Design, Singapore 487372, Singapore
      More by Xiaogang Liu
    • Ivan Aprahamian*
      Ivan Aprahamian
      6128 Burke Laboratory, Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755, United States
      *Email: [email protected]
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    Journal of the American Chemical Society

    Cite this: J. Am. Chem. Soc. 2025, 147, 18, 14930–14935
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    https://doi.org/10.1021/jacs.5c02183
    Published April 25, 2025
    Copyright © 2025 American Chemical Society

    Abstract

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    The length of the linker connecting a photoswitch to a material significantly influences the latter’s properties, with “zero-length” linkers being ideal for optimal photomodulation. The 1,2,3-triazole formed through the “click” reaction between an azide and an alkyne has been used as such a linking motif in various areas of research spanning from materials to biological chemistry. However, its effect, as well as that of its regioisomers, on the photoswitching properties has not been fully elucidated. Here, we report on a series of triazole-containing hydrazone photoswitches, investigating how the connectivity (1,4 vs 1,5) between the triazole and the switch affects the photoswitching properties. The structure–property analysis and DFT/TD-DFT calculations show that the switching efficiency of N-connected 1,4-triazole hydrazones is lower than their C-connected counterparts, while the 1,5-triazole hydrazone exhibits an overall better photoswitching efficiency.

    Copyright © 2025 American Chemical Society

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    Supporting Information

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    The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/jacs.5c02183.

    • General methods, experimental procedures, NMR spectra, single crystals, photoisomerization and kinetic studies in solution, theoretical calculations, and crystal data for 1-Z, 2-Z, 3-E, 4-E, 4-Z, and 5-Z (PDF)

    Accession Codes

    Deposition Numbers 2329305, 2329317, 2329375, 2329378, and 2329444 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via the joint Cambridge Crystallographic Data Centre (CCDC) and Fachinformationszentrum Karlsruhe Access Structures service.

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    Journal of the American Chemical Society

    Cite this: J. Am. Chem. Soc. 2025, 147, 18, 14930–14935
    Click to copy citationCitation copied!
    https://doi.org/10.1021/jacs.5c02183
    Published April 25, 2025
    Copyright © 2025 American Chemical Society

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