Literature DB >> 21410168

A simple but effective dual redox and fluorescent ion pair receptor based on a ferrocene-imidazopyrene dyad.

María Alfonso1, Arturo Espinosa, Alberto Tárraga, Pedro Molina.   

Abstract

The ferrocene-imidazopyrene dyad, bearing the imidazole ring as the only receptor site, acts as a redox and optical molecular sensor for ion pairs, exhibiting an easily detectable signal change in the redox potential of the ferrocene/ferrocinium redox couple and in the emission spectrum. Perturbation of the emission spectrum follows the order Pb(2+) > Hg(2+) > Zn(2+) for cations and H(2)PO(4)(-) > AcO(-) for anions.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID: 21410168     DOI: 10.1021/ol2004935

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

1.  Selective ratiometric fluorescence detection of acetate based on a novel Schiff base derivative.

Authors:  Ge Liu; Jie Shao
Journal:  J Fluoresc       Date:  2011-09-16       Impact factor: 2.217

2.  The structure of Cu(II) and Hg(II) complexes of bispyrenyl azine revisited.

Authors:  Arturo Espinosa Ferao; Rafaela García
Journal:  J Mol Model       Date:  2017-03-18       Impact factor: 1.810

3.  The first colorimetric receptor for the B4O7 2- anion based on nitro substituted phenanthroimidazole ferrocene derivatives.

Authors:  Pei Wu; Guo Wang; Lu Zhou; Jing Lu; Jianchun Wang
Journal:  RSC Adv       Date:  2018-01-19       Impact factor: 4.036

4.  Multifunctional Benzothiadiazole-Based Small Molecules Displaying Solvatochromism and Sensing Properties toward Nitroarenes, Anions, and Cations.

Authors:  María Alfonso; Arturo Espinosa; Alberto Tárraga; Pedro Molina
Journal:  ChemistryOpen       Date:  2014-09-26       Impact factor: 2.911

  4 in total

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