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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

Modified Electrodes and Electrochemical Systems Switchable by Temperature Changes

TL;DR: In this paper, an overview of extensive research efforts in the area of temperature-controlled electrochemical systems is presented, which is achieved by modification of electrode surfaces with thermo-sensitive polymers (e.g., poly(N-isopropylacrylamide), PNIPAM) which are reversibly switched by temperature changes between two different structures: swollen expanded coil conformation and shrunken collapsed globule state.
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Azobenzene Photoisomerization-Induced Destabilization of B-DNA

TL;DR: The conformational response of DNA upon azobenzene binding and isomerization is investigated, using a threoninol linker that has been experimentally investigated recently and nonequilibrium molecular dynamics simulations are carried out using a switching potential describing the photoinduced isomersization.
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A new room temperature dark conglomerate mesophase formed by bent-core molecules combining 4-iodoresorcinol with azobenzene units.

TL;DR: The first bent-core molecules comprising 4-iodoresorcinol as the central core unit and incorporating azobenzene units have been synthesized and a new type of dark conglomerate phase (DC phase) is observed, which remains over a wide temperature range down to room temperature without crystallization.
Journal ArticleDOI

Isomer Dependence on the Reactivity of Diazenes with Pentaphenylborole

TL;DR: Reactions of the anti-aromatic pentaphenylborole with diazenes indicate that both the substitution and the isomer influence the reaction outcome, and the more aromatic pyridazine proved to be less reactive, forming a resilient adduct.
Journal ArticleDOI

Cross-Coupling Strategy for the Synthesis of Diazocines.

TL;DR: This work presents a new synthetic strategy that is both versatile and reliable, and starting from widely available 2-bromobenzyl bromides, the designated molecules can be obtained in three simple steps.
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.
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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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