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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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The Halogen Bond

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Spiropyran-based dynamic materials

TL;DR: This review discusses the synthesis, switching conditions, and use of dynamic materials in which spiropyran has been attached to the surfaces of polymers, biomacromolecules, inorganic nanoparticles, as well as solid surfaces.
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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

Synthesis of the most intensely fluorescent azobenzene by utilizing the B–N interaction

TL;DR: A boron-substituted azobenzene, (E)-[2-(4-methoxyphenylazo)phenyl]bis(pentafluorophenyl)borane, presented the most intense fluorescence among the azOBenzene derivatives.
Journal ArticleDOI

Further evidence for rotation in the π,π and inversion in the n,π photoisomerization of azobenzenes

TL;DR: In this paper, the authors presented quantiques quantiques d'isomerisation trans-cis and cis-trans a 313 and 436 nm, respectively, for azobenzene.
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