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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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Journal ArticleDOI

A Straightforward Protocol for the Highly Efficient Preparation of Main-Chain Azo Polymers Directly from Bisnitroaromatic Compounds by the Photocatalytic Process

TL;DR: In this paper, the synthesis of main-chain Azo polymers directly from bisnitroaromatic compounds by the photocatalytic process has been achieved under mild conditions, which avoids the tedious synthesis of Azo monomers and proceeds with a high monomer conversion and excellent selectivity but without generating a significant amount of inorganic wastes and impurities.
Journal ArticleDOI

Photo-switched magnetic coupling in spin-crossover complexes.

TL;DR: The recent progress on the photoswitchable magnetic coupling in spin-crossover complexes reported by both the authors' group and other groups are discussed and the role of magnetic coupling is highlighted in determining their magnetic properties.
Journal ArticleDOI

Palladium-Catalyzed Oxidative Synthesis of Unsymmetrical Azophenols.

TL;DR: This study represents the first general method for the synthesis of o-hydroxyazobenzenes starting from simple azoarenes and tolerates various functional groups and allows the synthesisation of diverse unsymmetrical azophenols under mild conditions in good to excellent yields.
Journal ArticleDOI

Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles

TL;DR: New oxidative dehydrogenative couplings of pyrazol-5-amines for the selective synthesis of azopyrrole derivatives have been described and were employed by treatment with various terminal alkynes through Sonogashira cross-coupling leading to new azo compounds.
References
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Journal ArticleDOI

Photomechanics: directed bending of a polymer film by light.

TL;DR: It is shown that a single film of a liquid-crystal network containing an azobenzene chromophore can be repeatedly and precisely bent along any chosen direction by using linearly polarized light.
Journal ArticleDOI

A Reëxamination of the Hammett Equation.

H. H. Jaffé
- 01 Oct 1953 - 
Journal ArticleDOI

Light-driven motion of liquids on a photoresponsive surface

TL;DR: The light-driven motion of a fluid substance in a surface-modified glass tube suggests potential applicability to microscale chemical process systems.
Journal ArticleDOI

Design and synthesis of chromophores and polymers for electro-optic and photorefractive applications

TL;DR: The ability of nonlinear optical materials to transmit, process and store information forms the basis of emerging optoelectronic and photonic technologies as discussed by the authors, where organic chromophore-containing polymers, in which the refractive index can be controlled by light or an electric field, are expected to play an important role.
Journal ArticleDOI

Ultrafast Dynamics of Photochromic Systems.

TL;DR: Reaction dynamics of the photochromic systems such as spiropyran, flugide and diarylethene derivatives in femto- to nano-second time region was reviewed and mechanisms of rapid reaction channels in various phases were discussed.
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