Literature DB >> 29712397

Molecular Switching in the Near Infrared (NIR) with a Functionalized Boron-Dipyrromethene Dye.

Knut Rurack1, Matthias Kollmannsberger2, Jörg Daub2.   

Abstract

The highly fluorescent, unsymmetrically substituted boron-dipyrromethene dye 1 shows emission features that are strongly dependent on the solvent polarity. Thus, 1 can be used for highly sensitive fluorometric probing of solvent polarity and acidity and furthermore can be switched chemically or electrochemically in the near infrared.
© 2001 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.

Entities:  

Keywords:  donor-acceptor systems; electrochromism; fluorescence; molecular switches; solvatochromism

Year:  2001        PMID： 29712397     DOI： 10.1002/1521-3773(20010119)40:2<385::AID-ANIE385>3.0.CO;2-F

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


  3 in total

1.  Synthesis and Spectroscopic Investigation of a Series of Push-Pull Boron Dipyrromethenes (BODIPYs).

Authors:  Sunting Xuan; Ning Zhao; Xiangyi Ke; Zehua Zhou; Frank R Fronczek; Karl M Kadish; Kevin M Smith; M Graça H Vicente
Journal:  J Org Chem       Date:  2017-02-16       Impact factor: 4.354

2.  Excitation spectra of dibenzoborole containing pi-electron systems: controlling the electronic spectra by changing the p(pi)-pi* conjugation.

Authors:  Kanchana S Thanthiriwatte; Steven R Gwaltney
Journal:  J Phys Chem A       Date:  2006-02-23       Impact factor: 2.781

3.  GlycoBODIPYs: Sugars Serving as a Natural Stock for Water-soluble Fluorescent Probes of Complex Chiral Morphology.

Authors:  Lukas J Patalag; Somayeh Ahadi; Olesia Lashchuk; Peter G Jones; Simon Ebbinghaus; Daniel B Werz
Journal:  Angew Chem Int Ed Engl       Date:  2021-03-17       Impact factor: 15.336
  3 in total

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