Literature DB >> 20334366

Synthesis of spiropyrans as building blocks for molecular switches and dyads.

Christoph Beyer1, Hans-Achim Wagenknecht.   

Abstract

The synthesis of spiropyrans was improved significantly with use of ultrasonic radiation. To show the broad applicability of this methodology a range of spiropyrans were prepared which are equipped with iodo, hydroxyl, ethinyl, or azido groups as potential building blocks for conjugation to functional pi-systems or biopolymers. Representatively, the conjugation chemistry was demonstrated for the preparation of spiropyran conjugates with pyrene, perylene, and nile red via the "click"-type cycloaddition. These molecular dyads were characterized by optical spectroscopy.

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Year:  2010        PMID: 20334366     DOI: 10.1021/jo100309r

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  4 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.  Diarylethene-modified nucleotides for switching optical properties in DNA.

Authors:  Sebastian Barrois; Hans-Achim Wagenknecht
Journal:  Beilstein J Org Chem       Date:  2012-06-20       Impact factor: 2.883

3.  Preserving π-conjugation in covalently functionalized carbon nanotubes for optoelectronic applications.

Authors:  Antonio Setaro; Mohsen Adeli; Mareen Glaeske; Daniel Przyrembel; Timo Bisswanger; Georgy Gordeev; Federica Maschietto; Abbas Faghani; Beate Paulus; Martin Weinelt; Raul Arenal; Rainer Haag; Stephanie Reich
Journal:  Nat Commun       Date:  2017-01-30       Impact factor: 14.919

4.  Manipulating the fluorescence lifetime at the sub-cellular scale via photo-switchable barcoding.

Authors:  Yujie Xie; Maria C Arno; Jonathan T Husband; Miquel Torrent-Sucarrat; Rachel K O'Reilly
Journal:  Nat Commun       Date:  2020-05-18       Impact factor: 14.919

  4 in total

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