synthesis, binding and fluorescence studies of bis-2-amidopyrrole receptors for bis-carboxylate anions合成、绑定和荧光的研究bis-2-amidopyrrole bis-carboxylate阴离子受体.pdfVIP
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synthesis, binding and fluorescence studies of bis-2-amidopyrrole receptors for bis-carboxylate anions合成、绑定和荧光的研究bis-2-amidopyrrole bis-carboxylate阴离子受体
Sensors 2009, 9, 1534-1540; doi:10.3390/
OPEN ACCESS
sensors
ISSN 1424-8220
/journal/sensors
Communication
Synthesis, Binding and Fluorescence Studies of
Bis-2-amidopyrrole Receptors for Bis-carboxylate Anions
Belén Jiménez 1, Emilio Calle 2 and Cruz Caballero 1,*
1 Organic Chemistry Department, Plaza de los Caidos, 1-5, University of Salamanca, E-37008
Salamanca, Spain; E-Mail: belenjj@yahoo.es
2 Physical Chemistry Department. Plaza de los Caidos 1-5, University of Salamanca, E-37008
Salamanca, Spain; E-Mail: ecalle@usal.es
* Author to whom correspondence should be addressed; E-Mail: ccsa@usal.es; Tel.: +34-923-294481
Received: 12 February 2009; in revised form: 27 February 2009 / Accepted: 2 March 2009 /
Published: 4 March 2009
Abstract: The ditopic neutral receptors 1 and 2 were synthesized for the recognition and
sensing of bis-carboxylates. They are based on pyrrole and amide groups as hydrogen-bond
donors to bind the oxoanions of the guests. Among the obtained results, the selectivity for
glutarate over succinate is particularly interesting. Compound 1 behaves as a PET
fluorescence sensor for glutarate.
Keywords: Molecular recognition, bis-2-amidopyrrole receptors, bis-carboxylate anions,
fluorescent sensor; hydrogen bonding.
1. Introduction
The selective recognition and sensing of anions by synthetic host molecules has become an
important area of interest and activity in molecular recognition [1]. Among them, owing to their
chemical and biolo
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