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Highly Sensitive and Selective Fluorescent Probes for Cu(II) Detection Based on Calix[4]arene-Oxacyclophane Architectures

A new topological design of fluorescent probes for sensing copper ion is disclosed. The calix[4]arene-oxacyclophane (Calix-OCP) receptor, either wired-in-series in arylene-alt-ethynylene conjugated polymers or standing alone as a sole molecular probe, display a remarkable affinity and selectivity fo...

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Detalles Bibliográficos
Autores principales: Costa, Alexandra I., Barata, Patrícia D., Fialho, Carina B., Prata, José V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287820/
https://www.ncbi.nlm.nih.gov/pubmed/32466180
http://dx.doi.org/10.3390/molecules25102456
Descripción
Sumario:A new topological design of fluorescent probes for sensing copper ion is disclosed. The calix[4]arene-oxacyclophane (Calix-OCP) receptor, either wired-in-series in arylene-alt-ethynylene conjugated polymers or standing alone as a sole molecular probe, display a remarkable affinity and selectivity for Cu(II). The unique recognition properties of Calix-OCP system toward copper cation stem from its pre-organised cyclic array of O-ligands at the calixarene narrow rim, which is kept in a conformational rigid arrangement by a tethered oxacyclophane sub-unit. The magnitude of the binding constants (K(a) = 5.30 − 8.52 × 10(4) M(−1)) and the free energy changes for the inclusion complexation (−ΔG = 27.0 − 28.1 kJmol(−1)), retrieved from fluorimetric titration experiments, revealed a high sensitivity of Calix-OCP architectures for Cu(II) species. Formation of supramolecular inclusion complexes was evidenced from UV-Vis spectroscopy. The new Calix-OCP-conjugated polymers (polymers 4 and 5), synthesized in good yields by Sonogashira–Hagihara methodologies, exhibit high fluorescence quantum yields (Φ(F) = 0.59 − 0.65). Density functional theory (DFT) calculations were used to support the experimental findings. The fluorescence on–off behaviour of the sensing systems is tentatively explained by a photoinduced electron transfer mechanism.