In the recent decades, the investigations on photoresponsive molecular systems with multiple azoarenes are quite popular in diverse perspectives ranging from fundamental understanding of multiple photoswitches, supramolecular chemistry, and various application prospects. In fact, several insightful and conceptual designs of such systems were investigated with architectural distinctions. In particular, the demonstration of applications such as data storage with the help of multistate or orthogonal photoswitches, light modulation of catalysis via cooperative switching, sensors using supramolecular host-guest interactions, and materials such as liquid crystals, grating, actuators, etc. are some of the milestones in this area. Herein, we cover the recent advancements in the research areas of multiazoarenes containing systems that have been classified into Type-1 {linear, non-linear, and core-based (A)}, Type-2 {tripodal C -symmetric (C3)} and Type-3 {macrocyclic (M)} structural motifs.

Download full-text PDF

Source
http://dx.doi.org/10.1002/tcr.202200074DOI Listing

Publication Analysis

Top Keywords

multiple azoarenes
8
supramolecular chemistry
8
chemistry application
8
application prospects
8
azoarenes based
4
systems
4
based systems
4
systems photoswitching
4
photoswitching supramolecular
4
prospects decades
4

Similar Publications

Multiple control of azoquinoline based molecular photoswitches.

Chem Sci

February 2024

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences Fuzhou 350002 China

Multi-addressable molecular switches with high sophistication are creating intensive interest, but are challenging to control. Herein, we incorporated ring-chain dynamic covalent sites into azoquinoline scaffolds for the construction of multi-responsive and multi-state switching systems. The manipulation of ring-chain equilibrium by acid/base and dynamic covalent reactions with primary/secondary amines allowed the regulation of / photoisomerization.

View Article and Find Full Text PDF

Visible-Light Photoswitchable Benzimidazole Azo-Arenes as β-Arrestin2-Biased Selective Cannabinoid 2 Receptor Agonists.

Angew Chem Int Ed Engl

December 2023

Pharmazeutische und Medizinische Chemie, Institut für Pharmazie und Lebensmittelchemie, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.

The cannabinoid 2 receptor (CB R) has high therapeutic potential for multiple pathogenic processes, such as neuroinflammation. Pathway-selective ligands are needed to overcome the lack of clinical success and to elucidate correlations between pathways and their respective therapeutic effects. Herein, we report the design and synthesis of a photoswitchable scaffold based on the privileged structure of benzimidazole and its application as a functionally selective CB R "efficacy-switch".

View Article and Find Full Text PDF

In the recent decades, the investigations on photoresponsive molecular systems with multiple azoarenes are quite popular in diverse perspectives ranging from fundamental understanding of multiple photoswitches, supramolecular chemistry, and various application prospects. In fact, several insightful and conceptual designs of such systems were investigated with architectural distinctions. In particular, the demonstration of applications such as data storage with the help of multistate or orthogonal photoswitches, light modulation of catalysis via cooperative switching, sensors using supramolecular host-guest interactions, and materials such as liquid crystals, grating, actuators, etc.

View Article and Find Full Text PDF

Reversible Scavenging of Dioxygen from Air by a Copper Complex.

J Am Chem Soc

November 2021

Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States.

We report that exposing the dipyrrin complex (L)Cu(N) to air affords rapid, quantitative uptake of O in either solution or the solid-state to yield (L)Cu(O). The air and thermal stability of (L)Cu(O) is unparalleled in molecular copper-dioxygen coordination chemistry, attributable to the ligand flanking groups which preclude the [Cu(O)] core from degradation. Despite the apparent stability of (L)Cu(O), dioxygen binding is reversible over multiple cycles with competitive solvent exchange, thermal cycling, and redox manipulations.

View Article and Find Full Text PDF

Dinickel Active Sites Supported by Redox-Active Ligands.

Acc Chem Res

October 2021

Department of Chemistry, Purdue University, West Lafayette, Indiana 47907, United States.

Redox reactions that take place in enzymes and on the surfaces of heterogeneous catalysts often require active sites that contain multiple metals. By contrast, there are very few homogeneous catalysts with multinuclear active sites, and the field of organometallic chemistry continues to be dominated by the study of single metal systems. Multinuclear catalysts have the potential to display unique properties owing to their ability to cooperatively engage substrates.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!