Literature DB >> 16586525

pK(a) Switching induced by the change in the pi-conjugated system based on photochromism.

Yuka Odo1, Kenji Matsuda, Masahiro Irie.   

Abstract

Two diarylethene derivatives 1 a and 2 a containing a 2,5-diaryl-3-thienyl group have been designed and synthesized. The pK(a) values of these compounds change upon photoirradiation. They have a phenol group as a proton source and a pyridinium group as an acceptor unit at each end of the pi-conjugated chain. The cyclization/cycloreversion reactions can be used to control the length of the pi-conjugated chain between the proton source and the acceptor. The change in the pi-conjugated chain length caused the pK(a)-switching.

Entities:  

Year:  2006        PMID: 16586525     DOI: 10.1002/chem.200501292

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


  3 in total

1.  pH-dependent optical properties of synthetic fluorescent imidazoles.

Authors:  Mikhail Y Berezin; Jeff Kao; Samuel Achilefu
Journal:  Chemistry       Date:  2009       Impact factor: 5.236

2.  Proton-Gated Ring-Closure of a Negative Photochromic Azulene-Based Diarylethene.

Authors:  Ian Cheng-Yi Hou; Fabian Berger; Akimitsu Narita; Klaus Müllen; Stefan Hecht
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-19       Impact factor: 16.823

3.  Photoswitchable Nitrogen Superbases: Using Light for Reversible Carbon Dioxide Capture.

Authors:  Lukas F B Wilm; Mowpriya Das; Daniel Janssen-Müller; Christian Mück-Lichtenfeld; Frank Glorius; Fabian Dielmann
Journal:  Angew Chem Int Ed Engl       Date:  2021-11-26       Impact factor: 16.823

  3 in total

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