A Noncentrosymmetric Metal‐Free Borophosphate: Achieving a Large Birefringence and Excellent Stability by Covalent‐Linkage

Abstract

Organic–inorganic hybrid linear and nonlinear optical (NLO) materials have received increasingly wide spread attention in recent years. Herein, the first hybrid noncentrosymmetric (NCS) borophosphate, (C₅H₆N)₂B₂O(HPO₄)₂ (4PBP), is rationally designed and synthesized by a covalent‐linkage strategy. 4‐pyridyl‐boronic acid (4 PB) is considered as a bifunctional unit, which may effectively improve the optical properties and stability of the resultant material. On the one hand, 4 PB units are covalently linked with PO₃(OH) groups via strong B–O–P connections, which significantly enhances the thermal stability of 4PBP (decomposition at 321, vs lower 200 °C of most of hybrid materials). On the other hand, the planar π‐conjugated C₅H₆N units and their uniform layered arrangements represent large structural anisotropy and hyperpolarizability, achieving the largest birefringence (0.156 @ 546 nm) in the reported borophosphates and a second‐harmonic generation response (0.7 × KDP). 4PBP also exhibits a wide transparency range (0.27–1.50 µm). This work not only provides a promising birefringent material, but also offers a practical covalent‐attachment strategy for the rational design of new high‐performance optical materials.