Literature DB >> 20165790

A quinolinium-derived turn-off fluorescent anion sensor.

Adam N Swinburne1, Martin J Paterson, Andrew Beeby, Jonathan W Steed.   

Abstract

A quinolinium-derived anion sensor has been synthesised which shows a turn-off fluorescence response in the presence of anions, with selectivity for acetate. The compound exhibits complex anion binding comprising of a host dimer, 2 : 1 and 1 : 1 host : guest species. Fluorescent quenching is due to both dynamic and static processes with charge transfer being the dominant mechanism.

Entities:  

Year:  2010        PMID: 20165790     DOI: 10.1039/b919821k

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


  2 in total

1.  Speciation, luminescence, and alkaline fluorescence quenching of 4-(2-methylbutyl)aminodipicolinic acid (H2MEBADPA).

Authors:  Andrew J Ingram; Alexander G Dunlap; Richard Dipietro; Gilles Muller
Journal:  J Phys Chem A       Date:  2011-06-16       Impact factor: 2.781

Review 2.  Arylethynyl receptors for neutral molecules and anions: emerging applications in cellular imaging.

Authors:  Calden N Carroll; John J Naleway; Michael M Haley; Darren W Johnson
Journal:  Chem Soc Rev       Date:  2010-08-31       Impact factor: 54.564

  2 in total

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