Literature DB >> 17377685

Molecular switch based on a cucurbit[6]uril containing bistable [3]rotaxane.

Dönüs Tuncel1, Ozgür Ozsar, H Burak Tiftik, Bekir Salih.   

Abstract

A bistable CB6-based [3]rotaxane with two recognition sites has been prepared very efficiently in a high yield synthesis through CB6 catalyzed 1,3-dipolar cycloaddition; this rotaxane behaves as a reversible molecular switch and exhibits conformational changes caused by the movement of rings under base, acid and heat stimuli from one location to the other.

Entities:  

Year:  2007        PMID: 17377685     DOI: 10.1039/b616764k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Facile syntheses of [3]-, [4]- and [6]catenanes templated by orthogonal supramolecular interactions.

Authors:  Kai Wang; Chi-Chung Yee; Ho Yu Au-Yeung
Journal:  Chem Sci       Date:  2016-01-15       Impact factor: 9.825

2.  Efficient catenane synthesis by cucurbit[6]uril-mediated azide-alkyne cycloaddition.

Authors:  Antony Wing Hung Ng; Chi-Chung Yee; Kai Wang; Ho Yu Au-Yeung
Journal:  Beilstein J Org Chem       Date:  2018-07-20       Impact factor: 2.883

3.  Relative contractile motion of the rings in a switchable palindromic [3]rotaxane in aqueous solution driven by radical-pairing interactions.

Authors:  Leah S Witus; Karel J Hartlieb; Yuping Wang; Aleksandrs Prokofjevs; Marco Frasconi; Jonathan C Barnes; Edward J Dale; Albert C Fahrenbach; J Fraser Stoddart
Journal:  Org Biomol Chem       Date:  2014-08-28       Impact factor: 3.876

  3 in total

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