RESUMO
Photoluminescence activity of coordination polymers (CPs) has evoked intricate applications in the field of materials science, especially sensing of ions/molecules. In the present study, 2,3,5,6-tetrakis(2-pyridyl)pyrazine (tppz) and 5-aminoisophthalate (HAIPA-) coordinated to Cd(II) to architect a coordination polymer, {[Cd(HAIPA)(tppz)(OH)]·3H2O}n (CP1) which unveils blue emission in an aqueous acetonitrile (98% aqueous) suspension. The emission is selectively quenched by Pd2+ only without interference in the presence of as many as 16 other cations. The structure of CP1 shows the presence of a free -COOH group, and the interlayer (-CO)O(2)···O(7) (OC-) distance, 4.242 Å, along with the π···π interactions (3.990, 3.927 Å), may make a cavity which suitably accommodates only Pd2+ (van der Waal's radius, 1.7 Å) through the Pd(II)-carboxylato (-COO-Pd) coordination. The stability of the composite, [CP1 + Pd2+] may be assessed from the fluorescence quenching experiment, and the Stern-Volmer constant (KSV) is 7.2 × 104 M-1. Therefore, the compound, CP1, is a promising sensor for Pd(II) in a selective manner with limit of detection (LOD), 0.08 µM. The XPS spectra of CP1 and [CP1 + Pd2+] have proven the presence of Pd2+ in the host and the existence of a coordinated -COO-Pd bond. Interestingly, inclusion of Pd2+ in CP1 decreases the band gap from 3.61 eV (CP1) to 3.05 eV ([CP1 + Pd2+]) which lies in the semiconducting region and has exhibited improved electrical conductivity from 7.42 × 10-5 (CP1) to 1.20 × 10-4 S m-1 ([CP1 + Pd2+]). Upon light irradiation, the electrical conductivities are enhanced to 1.45 × 10-4 S m-1 (CP1) and 3.81 × 10-4 S m-1 ([CP1 + Pd2+]); which validates the highly desired photoresponsive device applications. Therefore, such type of materials may serve as SDG-army (sustainable development goal) to battle against the environmental issues and energy crisis.
