New polyacetylene-based chemosensory materials for the “turn-on” sensing of α-amino acids

For the first time, a new disubstituted polyacetylene (P1) was utilized to sense α-amino acids based on a “turn-on” model, through an indirect approach. Thus, first, the strong blue fluorescence of P1 was quenched by trace copper ions efficiently, then the addition of α-amino acids to the P1/Cu2+ co...

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Bibliographic Details
Published in:Polymer (Guilford) 2009-01, Vol.50 (2), p.434-440
Main Authors: Zeng, Qi, Zhang, Liyao, Li, Zhen, Qin, Jingui, Tang, Ben Zhong
Format: Article
Language:English
Subjects:
Applied sciences
Chemosensor
Exact sciences and technology
Fluorescence “turn-on”
Organic polymers
Physicochemistry of polymers
Polyacetylene
Polymers with particular properties
Preparation, kinetics, thermodynamics, mechanism and catalysts
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Summary:For the first time, a new disubstituted polyacetylene (P1) was utilized to sense α-amino acids based on a “turn-on” model, through an indirect approach. Thus, first, the strong blue fluorescence of P1 was quenched by trace copper ions efficiently, then the addition of α-amino acids to the P1/Cu2+ complex could recover the strong fluorescence of P1 to report the presence of α-amino acids. Interestingly, the P1/Cu2+ complex demonstrated much higher sensitivity towards histidine, with the detection limit of ∼2ppm (∼1.3×10−5mol/L). With the aid of a normal UV lamp, histidine could be differed from other α-amino acids visually by the observation of its strong blue fluorescence, at the concentration as low as 4.0×10−5mol/L. Due to the convenient synthesis of P1, and the so far reported many other conjugated fluorescent polymers, the work reported here might open up a new avenue to develop new biosensors. [Display omitted]
ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2008.11.009