| Summary: | Single-crystal solid–liquid dual-phase hybrid organic–inorganic ligand frameworks with reversible sensing response facilitated by external stimuli have received significant attention in recent years. This report presents a significant leap in designing electronic structures that display reversible dual-phase photoluminescence properties from single-crystal hybrid ligand frameworks. Three-dimensional Cu(C<sub>3</sub>N<sub>2</sub>H<sub>4</sub>)<sub>4</sub>Cl<sub>2</sub> complex frameworks were formed through the intermolecular hydrogen bonding and π⋯π stacking supramolecular interactions. The absorption band peaks at 627 nm were assigned to d–d transition showing 10Dq = 15,949 cm<sup>−1</sup> and crystal field stabilization energy (CFSE) = 0.6 × 10Dq = 114.4 kJmol<sup>−1</sup>, while the ligand-to-metal charge transfer (LMCT) of complexes was displayed at 292 nm. The intense luminescence band results from LMCT present at 397 nm. Considering its structure, air stability, framework forming and stable luminescence in aqueous solution, the Cu(C<sub>3</sub>N<sub>2</sub>H<sub>4</sub>)<sub>4</sub>Cl<sub>2</sub> complex shows potential for luminescence Cu-based sensors using emission intensity to detect heavy metal ion species.
|
|---|