MIPdatabase
Authors: Longo L, Vasapollo G, Scardino A, Picca RA, Malitesta C
Article Title: Synthesis of a new substituted zinc phthalocyanine as functional monomer in the preparation of MIPs.
Publication date: 2006
Journal: Journal of Porphyrins and Phthalocyanines
Volume: 10
Issue: (8)
Page numbers: 1061-1065.
DOI: 10.1142/S1088424606000417
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 (-Δ G0) were calculated according to the modified Benesi-Hildebrand equation. Binding experiments showed that Ka of phthalocyanine with tri-O-acetyladenosine (TOAA) is 1.35 x 10^4, 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
Template and target information: tri-O-acetyladenosine, TOAA
Author keywords: artificial receptors, Benesi-hildebrand equation, MIPs, Nucleosides, Phthalocyanine
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