Literature DB >> 26662470

Switching Diarylethenes Reliably in Both Directions with Visible Light.

Sebastian Fredrich1, Robert Göstl1, Martin Herder1, Lutz Grubert1, Stefan Hecht2.   

Abstract

A diarylethene photoswitch was covalently connected to two small triplet sensitizer moieties in a conjugated and nonconjugated fashion and the photochromic performance of the resulting compounds was investigated. In comparison with the parent diarylethene (without sensitizers) and one featuring saturated linkages, the conjugated photoswitch offers superior fatigue resistance upon visible-light excitation due to effective triplet energy transfer from the biacetyl termini to the diarylethene core. Our design makes it possible to switch diarylethenes with visible light in both directions in a highly efficient and robust fashion based on extending π-conjugation and by-product-free ring-closure via the triplet manifold.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  diarylethenes; photochromism; sensitizers; singlet oxygen

Year:  2015        PMID: 26662470     DOI: 10.1002/anie.201509875

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  9 in total

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7.  Photoswitching of Local (Anti)Aromaticity in Biphenylene-Based Diarylethene Molecular Switches.

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8.  Computational and Crystallographic Examination of Naphthoquinone Based Diarylethene Photochromes.

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9.  Toward Two-Photon Absorbing Dyes with Unusually Potentiated Nonlinear Fluorescence Response.

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