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.

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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
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article

Advances in Molecular Photoswitches: From Azobenzenes to Azoquinolines

Jacek E. Nycz, Nataliya Karaush‐Karmazin
4 citations
Current Organic Chemistry
Photochromic and Fluorescence Chemistry
0.47
article

Advances in Molecular Photoswitches: From Azobenzenes to Azoquinolines

Jacek E. Nycz, Nataliya Karaush‐Karmazin
article en
4 citations

Abstract

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.

Current Organic ChemistryVol. 29(15)
Cherkasy National University (UA), University of Silesia in Katowice (PL)
Industry, innovation and infrastructure
Openalex Percentile: Top 38%
Photochromic and Fluorescence Chemistry
0.47
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Advances in Molecular Photoswitches: From Azobenzenes to Azoquinolines — Jacek E. Nycz, Nataliya Karaush‐Karmazin · Current Organic Chemistry (2024) | TGRS Research Map | TGRS