Literature DB >> 23033200

Sterically crowding the bridge of dithienylcyclopentenes for enhanced photoswitching performance.

Robert Göstl1, Björn Kobin, Lutz Grubert, Michael Pätzel, Stefan Hecht.   

Abstract

Better switching: The introduction of bulky substituents into the bridge moiety of dithienylethenes led to derivatives exhibiting high photocyclization quantum yields. This novel and versatile form of substitution facilitated tuning of the switching performance without compromising on the optical and redox properties of the ring-open and ring-closed forms (see scheme).
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Year:  2012        PMID: 23033200     DOI: 10.1002/chem.201203111

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

Review 1.  Molecular photoswitches in aqueous environments.

Authors:  Jana Volarić; Wiktor Szymanski; Nadja A Simeth; Ben L Feringa
Journal:  Chem Soc Rev       Date:  2021-11-15       Impact factor: 54.564

2.  Enantiospecific photoresponse of sterically hindered diarylethenes for chiroptical switches and photomemories.

Authors:  Wenlong Li; Xin Li; Yongshu Xie; Yue Wu; Mengqi Li; Xin-Yan Wu; Wei-Hong Zhu; He Tian
Journal:  Sci Rep       Date:  2015-03-17       Impact factor: 4.379

  2 in total

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