A new zinc phthalocyanine peripherally substituted with methacrylic groups was synthesized to be employed as a functional monomer in the formation of molecularly imprinted polymers as nucleoside receptors. The binding affinity and selectivity of the synthesized phthalocyanine towards nucleosides were evaluated by UV-vis titration experiments in CH2Cl2 at 298 K. The binding constant (Ka) and Gibbs free energy changes (-ΔG0) were calculated according to the modified Benesi-Hildebrand equation. Binding experiments showed that Ka of phthalocyanine with tri-O-acetyladenosine (TOAA) is 1.35 × 104, 500 times that of phthalocyanine with tri-O-acetyluridine (TOAU), indicating a high selectivity of the synthesized phthalocyanine derivative. Copyright © 2006 Society of Porphyrins & Phthalocyanines.

Synthesis of a new substituted zinc phthalocyanine as functional monomer in the preparation of MIPs

Picca R. A.;
2006

Abstract

A new zinc phthalocyanine peripherally substituted with methacrylic groups was synthesized to be employed as a functional monomer in the formation of molecularly imprinted polymers as nucleoside receptors. The binding affinity and selectivity of the synthesized phthalocyanine towards nucleosides were evaluated by UV-vis titration experiments in CH2Cl2 at 298 K. The binding constant (Ka) and Gibbs free energy changes (-ΔG0) were calculated according to the modified Benesi-Hildebrand equation. Binding experiments showed that Ka of phthalocyanine with tri-O-acetyladenosine (TOAA) is 1.35 × 104, 500 times that of phthalocyanine with tri-O-acetyluridine (TOAU), indicating a high selectivity of the synthesized phthalocyanine derivative. Copyright © 2006 Society of Porphyrins & Phthalocyanines.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11586/232869
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