A strongly fluorescent Ni complex with 2-(2-hy-droxy-eth-yl)pyridine ligands: synthesis, characterization and theoretical analysis and comparison with a related polymeric Cu complex.

The synthesis and characterization of di-aqua-bis-[2-(2-hy-droxy-eth-yl)pyridine-κ,)nickel(II) dinitrate, [Ni(CHNO)(HO)](NO), under ambient conditions is reported and compared with -poly[[bis-[2-(2-hy-droxy-eth-yl)pyridine-κ,]copper(II)]-μ-sulfato-κ:'], [Cu(CHNO)(SO)] [Zegh-ouan (2016 ▸). Private communication (refcode 1481676). CCDC, Cambridge, England]. In the two complexes, the 2-(2-hy-droxy-eth-yl)pyridine ligands coordinate the metal ions through the N atom of the pyridine ring and the O atom of the hy-droxy group, creating a chelate ring. The Ni or Cu ion lies on an inversion centre and exhibits a slightly distorted ON octa-hedral coordination geometry, build up by O and N atoms from two 2-(2-hy-droxy-eth-yl)pyridine ligands and two water mol-ecules or two O atoms belonging to sulfate anions. The sulfate anion bridges the Cu ions, forming a polymeric chain. The photoluminescence properties of these complexes have been studied on as-synthesized samples and reveal that both compounds display a strong blue-light emission with maxima around 497 nm. From DFT/TDDFT studies, the blue emission appears to be derived from the ligand-to-metal charge-transfer (LMCT) excited state. In addition, the IR spectroscopic properties and thermogravimetric behaviours of both complexes have been investigated.