Advances in Molecular Photoswitches: From Azobenzenes to Azoquinolines
Molecular photoswitches represent a dynamic and ever-growing research area based on the ability of molecules to convert (switch) between <i>cis-(Z)</i> and <i>trans-(E)</i> isomers. Azobenzenes are the most popular and widely employed <i>Z-E</i> photoswitchable molecules in the development of photoresponsive, multifunctional smart materials for various applications. The promising avenues in this field include molecular fine-tuning of azobenzenebased photoswitches and the creation of single or dual-functional probes. This short overview highlights recent advances in the design of molecular photoswitches, particularly the molecular design strategies of azobenzene-based photoswitches with their structural and electronic features. Particular attention is paid to azoquinolines, which seem to be a promising alternative to azobenzenes in the design of novel multifunctional photoswitches with improved photochromic properties. Here, we have also developed the novel star-shaped multiazoquinoline photoswitch comprising individual azoquinoline-based photochromes connected to a central trisubstituted 1,3,5- triformylphloroglucinol core by quantum chemical calculations. This unique structure is favorable for independent <i>Z-E</i> isomerization of each azoquinoline-based photochrome within one macromolecule.
Authors
- Jacek E. Nycz (ORCID: https://orcid.org/0000-0002-0992-1960)
- Nataliya Karaush‐Karmazin (ORCID: https://orcid.org/0000-0001-9360-2593)
Institutions
- Cherkasy National University (UA)
- University of Silesia in Katowice (PL)
Publication Details
- Journal
- Current Organic Chemistry
- Published
- 2024-10-23
- DOI
- https://doi.org/10.2174/0113852728344412241008083512
- Citations
- 4
- Primary Topic
- Photochromic and Fluorescence Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.47