From centrosymmetric CN3H6C6H5SO3 to non-centrosymmetric CN3H6C6H4SO3(OH): Hydroxyl introduced hydrogen bond reconstruction to realize strong second harmonic generation
Non-centrosymmetric (NCS) crystalline structures, critical for second harmonic generation (SHG) in all-solid-state lasers, are far less prevalent than their centrosymmetric (CS) counterparts. In this study, we report a structural transformation from CS to NCS configuration in benzenesulfonate derivatives via hydroxyl group incorporation, as illustrated by the transition in the newly discovered CN3H6C6H5SO3 (CS) and CN3H6C6H4SO3(OH) (NCS). The introduced hydroxyl groups induce hydrogen bond reconstruction, effectively breaking the original centrosymmetry. The resulting NCS compound exhibits remarkable nonlinear optical (NLO) properties, including a strong SHG response (1.6 × KDP with the particle sizes of 200-250 um), a wide bandgap (UV cutoff at 290 nm, corresponding band gap is 4.37 eV), and a large birefringence (0.21@1064nm), demonstrating excellent potential as an UV NLO crystal material.