“Clicked” Hydrazone PhotoswitchesClick to copy article linkArticle link copied!
- Daniil SosninDaniil Sosnin6128 Burke Laboratory, Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755, United StatesMore by Daniil Sosnin
- Mohammad IzadyarMohammad IzadyarFluorescence Research Group, Singapore University of Technology and Design, Singapore 487372, SingaporeMore by Mohammad Izadyar
- Syed Ali Abbas AbediSyed Ali Abbas AbediFluorescence Research Group, Singapore University of Technology and Design, Singapore 487372, SingaporeMore by Syed Ali Abbas Abedi
- Xiaogang LiuXiaogang LiuFluorescence Research Group, Singapore University of Technology and Design, Singapore 487372, SingaporeMore by Xiaogang Liu
- Ivan Aprahamian*Ivan Aprahamian*Email: [email protected]6128 Burke Laboratory, Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755, United StatesMore by Ivan Aprahamian
Abstract

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.
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