4′–phenyl −2, 2′: 6′, 2′’-terpyridine derivatives as metal chemosensors. Chelation and fluorescence capabilities towards Zn(II), Cd(II), and Hg(II) from experiment and theory

• Published in: Journal of photochemistry and photobiology. A, Chemistry. Chemistry., 2024-12, Vol.457, p.115885, Article 115885
• Main Authors: Rojas-Poblete, Macarena, Guajardo-Maturana, Raúl, Velásquez, Luis, Cantero-López, Plinio, Muñoz-Castro, Álvaro
• Format: Article
• Language: English
• Subjects: DFT calculation; Metal ligand interaction; Terpyridines
• ISSN: 1010-6030
• DOI: 10.1016/j.jphotochem.2024.115885

•4′-phenylterpyridine, synthesis, and theoretical studies toward metal-sensor properties.•4′-phenylterpyridine derivatives are multifunctional chemosensor of Zn2+, Cd2+, Hg2+ ions.•Host-guest interaction selectivity study of Zn2+, Cd2+, Hg2+ ions.•Research of optical features, including ground and excited estates from the TD-DFT methodologies.•Structural characteristics and EDA-NOCV calculations to unraveling the metal–ligand interactions and the sensor capabilities for organic and metal–ligand complexes. 4′-phenylterpyridine (TPY) involves four conjugated rings, leading to a multi-resonant chromophore with exceptional luminescent features. Further functionalization of the 4′-phenyl moiety enables a versatile set of chemosensors. In the series, the optical transitions remain similar, where λmax ranges from 253 to 269 nm, with emissions from 357 to 365 nm. Calculations of the natural transition orbitals NTOs deliver the localized hole-electron densities, indicating that the electronic transitions vary as a local-excitation (LE), charge transfer (CT), and mixed LE-CT along with the set. We employ the energy decomposition analysis to evaluate the possible coordination toward Zn(II), Cd(II), and Hg(II) cations, showing a favorable formation of complexes, where the interaction nature exhibits a ∼ 49 and ∼ 50 % electrostatic and orbital character for the Zn(II), Cd(II) and Hg(II) centers. Furthermore, the density deformation channels confer an explicit picture of the bonding scheme, denoting π- and σ-bonding contributions.