Literature DB >> 25758666

"Off-on" aggregation-based fluorescent sensor for the detection of chloride in water.

Michelle M Watt1, Jeffrey M Engle, Kurtis C Fairley, Timothy E Robitshek, Michael M Haley, Darren W Johnson.   

Abstract

Receptors selective for anions in aqueous media are a crucial component in the detection of anions for biological and environmental applications. Recent sensor designs have taken advantage of systems known to aggregate in solution, eliciting a fluorescent response. Herein, we demonstrate a chloride-selective fluorescent response of receptor 1(+), based on our well-established class of 2,6-bis(2-anilinoethynyl)pyridine bisureas. The fluorescence intensity ratio of 1(+)·Cl(->) aggregates in water is four times larger than the next most fluorescent anion complex, 1(+)·ClO4(->). In addition, (1)H NMR spectroscopic titrations demonstrate 1(+) binds chloride more strongly than other biologically relevant anions in solutions of both DMSO-d6 and 50/50 DMSO-d6/MeCN-d3.

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Year:  2015        PMID: 25758666      PMCID: PMC4537155          DOI: 10.1039/c4ob02409e

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


  26 in total

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4.  Molecular Self Assembly: Solvent Guests Tune the Conformation of a Series of 2,6-Bis(2-anilinoethynyl)pyridine-Based Ureas.

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7.  Anion-dependent fluorescence in bis(anilinoethynyl)pyridine derivatives: switchable ON-OFF and OFF-ON responses.

Authors:  Calden N Carroll; Brian A Coombs; Sean P McClintock; Charles A Johnson; Orion B Berryman; Darren W Johnson; Michael M Haley
Journal:  Chem Commun (Camb)       Date:  2011-04-07       Impact factor: 6.222

8.  Synthesis and optoelectronic properties of 2,6-bis(2-anilinoethynyl)pyridine scaffolds.

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9.  Protonation activates anion binding and alters binding selectivity in new inherently fluorescent 2,6-bis(2-anilinoethynyl)pyridine bisureas.

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