Quadruple-Bidentate Nitrate-Ligated A2 Hg(NO3 )4 (A=K, Rb): Strong Second-Harmonic Generation and Sufficient Birefringence.

Abstract

The design of efficient nonlinear optical (NLO) crystals continues to pose significant challenges due to the difficulty of assembling polar NLO-active modules in an optimal additive fashion. We report herein the first NLO-active mercuric nitrates A2 Hg(NO3 )4 (A=(KHNO), Rb (RHNO)), for which assembly is induced by ionic polarization of the d10 cations. The two new crystalline compounds are isostructural, featuring interesting pseudo-diamond-like structures with parallel [Hg(NO3 )4 ] modules, and leading to strong powder second-harmonic generation (SHG) responses of 9.2 (KHNO) and 8.8 (RHNO) times that of KH2 PO4 . In combination with the simple solution preparation of centimeter-scale crystals, sufficient birefringence, and short ultraviolet (UV) cutoff edges, these attributes make KHNO and RHNO promising candidates for UV NLO materials. Theoretical calculations and single-crystal structure analysis reveal that the newly-developed highly condensed and distorted [Hg(NO3 )4 ] module, with an Hg2+ cation that is quadruply bidentate nitrate-ligated, is crucial for the significant SHG responses. This work highlights the potential importance of modules with multiple bidentate ligands for the development of high-performing next-generation NLO materials.