Abstract

Four new potassium vanadyl iodates based on lone-pair-containing IO(3) and second-order Jahn-Teller distorted VO(5) or VO(6) asymmetric units, namely, α-KVO(2)(IO(3))(2)(H(2)O) (Pbca), β-KVO(2)(IO(3))(2)(H(2)O) (P2(1)2(1)2(1)), K(4)[(VO)(IO(3))(5)](2)(HIO(3))(H(2)O)(2)·H(2)O (P1), and K(VO)(2)O(2)(IO(3))(3) (Ima2) have been successfully synthesized by hydrothermal reactions. α-KVO(2)(IO(3))(2)(H(2)O) and β-KVO(2)(IO(3))(2)(H(2)O) exhibit two different types of 1D [VO(2)(IO(3))(2)](-) anionic chains. Neighboring VO(6) octahedra in the α-phase are corner-sharing into a 1D chain with the IO(3) groups attached on both sides of the chain in a uni- or bidentate bridging fashion, whereas those of VO(5) polyhedra in the β-phase are bridged by IO(3) groups into a right-handed helical chain with remaining IO(3) groups being grafted unidentately on both sides of the helical chain. The structure of K(4)[(VO)(IO(3))(5)](2)(HIO(3))(H(2)O)(2)·H(2)O contains novel isolated [(VO)(IO(3))(5)](2-) units composed of one VO(6) octahedron linked to five IO(3) groups and one terminal O(2-) anion. The structure of K(VO)(2)O(2)(IO(3))(3) exhibits a 1D [(VO)(2)O(2)(IO(3))(3)](-) chain in which neighboring VO(6) octahedra are interconnected by both oxo and bridging iodate anions. Most interestingly, three of four compounds are noncentrosymmetric (NCS), and K(VO)(2)O(2)(IO(3))(3) displays a very strong second-harmonic generation response of about 3.6 × KTP, which is phase matchable. It also has high thermal stability, a wide transparent region and moderate hardness as well as an excellent growth habit. Thermal analyses and optical and ferroelectric properties as well as theoretical calculations have also been performed.

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