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Journal ArticleDOI

Photoisomerization in different classes of azobenzene

TLDR
This critical review details the studies completed to date on the 3 main classes of azobenzene derivatives and explains the mechanism behind the isomerization mechanism.
Abstract
Azobenzene undergoes trans → cisisomerization when irradiated with light tuned to an appropriate wavelength. The reverse cis →transisomerization can be driven by light or occurs thermally in the dark. Azobenzene's photochromatic properties make it an ideal component of numerous molecular devices and functional materials. Despite the abundance of application-driven research, azobenzene photochemistry and the isomerization mechanism remain topics of investigation. Additional substituents on the azobenzene ring system change the spectroscopic properties and isomerization mechanism. This critical review details the studies completed to date on the 3 main classes of azobenzene derivatives. Understanding the differences in photochemistry, which originate from substitution, is imperative in exploiting azobenzene in the desired applications.

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Citations
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Spiropyran-based dynamic materials

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Stimuli-responsive supramolecular polymeric materials.

TL;DR: This critical review of recent developments in supramolecular polymeric materials is addressed, which can respond to appropriate external stimuli at the fundamental level due to the existence of noncovalent interactions of the building blocks.
References
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Journal ArticleDOI

Quenching and Recovery of Fluorescence of Azobenzenes by Acid–Base Reactions

TL;DR: In this article, a hybrid 2-borylazobenzene and pH-responsive 4-(dimethylamino)azobensene was synthesized as a hybrid.
Journal ArticleDOI

Saturation effect in azobenzene polymers used for polarization holography

TL;DR: In this paper, the saturation model of the polyester material can be used for the computer simulation of a polarization holographic data storage system under development, which is based on fast Fourier transforms, taking the parameters of the recording material and the optical processes into account.
Journal ArticleDOI

Trans-to-cis isomerization of stilbene following an ultrafast laser pulse

TL;DR: In this article, a trans-to-cis photoisomerization of stilbene induced by a femtosecond-scale laser pulse is described, showing that the basic mechanism is the simplest imaginable: Electronic excitation by the laser pulse weakens the central C-C bond, and also excites vibrations of this bond.
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