Solid-State Nonlinear Optical Properties of Mononuclear Copper(II) Complexes with Chiral Tridentate and Tetradentate Schiff Base Ligands

Salen-type metal complexes have been actively studied for their nonlinear optical (NLO) properties, and push-pull compounds with charge asymmetry generated by electron releasing and withdrawing groups have shown promising results. As a continuation of our research in this field and aiming at solid-state features, herein we report on the synthesis of mononuclear copper(II) derivatives bearing either tridentate N(2)O Schiff bases L((a−c)−) and pyridine as the forth ancillary ligand, [Cu(L(a−c))(py)](ClO(4)) (1a–c), or unsymmetrically-substituted push-pull tetradentate N(2)O(2) Schiff base ligands, [Cu(5-A-5′-D-saldpen/chxn)] (2a–c), both derived from 5-substituted salicylaldehydes (sal) and the diamines (1R,2R)-1,2-diphenylethanediamine (dpen) and (1S,2S)-1,2-diaminocyclohexane (chxn). All compounds were characterized through elemental analysis, infrared and UV/visible spectroscopies, and mass spectrometry in order to guarantee their purity and assess their charge transfer properties. The structures of 1a–c were determined via single-crystal X-ray diffraction studies. The geometries of cations of 1a–c and of molecules 2a–c were optimized through DFT calculations. The solid-state NLO behavior was measured by the Kurtz–Perry powder technique @1.907 µm. All chiral derivatives possess non-zero quadratic electric susceptibility (χ((2))) and an efficiency of about 0.15–0.45 times that of standard urea.