Literature DB >> 16604221

Anion-templated assembly of [2]rotaxanes.

Mark R Sambrook1, Paul D Beer, Michael D Lankshear, R Frederick Ludlow, James A Wisner.   

Abstract

Anion templation is used to develop a general method for rotaxane synthesis. The anion-templated synthesis of three new [2]rotaxanes containing positively charged pyridinium axles and neutral isophthalamide macrocyclic components is described. The incorporation of electron withdrawing substituents, such as the nitro group, into the 5-position of an isophthalamide bis-vinyl acyclic precursor results in a significant improvement in [2]rotaxane assembly yields. Rotaxane anion binding strengths are also enhanced whilst the rotaxane's unique interlocked binding domain ensures selectivity for chloride--the templating anion--is maintained.

Entities:  

Year:  2006        PMID: 16604221     DOI: 10.1039/b518178j

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Anion sensing by solution- and surface-assembled osmium(II) bipyridyl rotaxanes.

Authors:  Joshua Lehr; Thomas Lang; Octavia A Blackburn; Timothy A Barendt; Stephen Faulkner; Jason J Davis; Paul D Beer
Journal:  Chemistry       Date:  2013-10-14       Impact factor: 5.236

2.  Hydroxy Groups Enhance [2]Rotaxane Anion Binding Selectivity.

Authors:  Rosemary J Goodwin; Andrew Docker; Hugo I MacDermott-Opeskin; Heather M Aitken; Megan L O'Mara; Paul D Beer; Nicholas G White
Journal:  Chemistry       Date:  2022-04-05       Impact factor: 5.020

  2 in total

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