Macroscopic polarity control with alkali metal cation size and coordination environment in a series of tin iodates
- Authors
- Kim, Yeong Hun; Tran, T. Thao; Halasyamani, Shiv; Ok, Kang Min
- Issue Date
- Apr-2015
- Publisher
- CHINESE CHEMICAL SOC
- Citation
- INORGANIC CHEMISTRY FRONTIERS, v.2, no.4, pp 361 - 368
- Pages
- 8
- Journal Title
- INORGANIC CHEMISTRY FRONTIERS
- Volume
- 2
- Number
- 4
- Start Page
- 361
- End Page
- 368
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/11446
- DOI
- 10.1039/c4qi00243a
- ISSN
- 2052-1553
2052-1553
- Abstract
- A series of stoichiometrically similar tin(IV) iodates, A(2)Sn(IO3)(6) (A = Li, Na, K, Rb, Cs) and Sn2+Sn4+(IO3)(6) have been hydrothermally synthesized. X-ray diffraction was used to determine the crystal structures of the reported materials. All six materials reveal zero-dimensional molecular structures that consist of SnO6 octahedra and IO3 polyhedra. However, the size and coordination environment of cations significantly influence the macroscopic centricities of the materials. While Li2Sn(IO3)(6) and Na2Sn(IO3)(6) crystallize in the noncentrosymmetric (NCS) polar space group, P6(3), the K, Rb, Cs, and Sn phases crystallize in the centrosymmetric (CS) nonpolar space group, R (3) over bar. Infrared and UV-vis spectroscopy, thermal analyses, and local dipole moment calculations are reported. With NCS polar materials, powder second-harmonic generation (SHG) properties, polarization, and piezoelectric measurements are also presented. The NCS properties are mainly attributable to the parallel alignment of the lone pairs in I5+ cations.
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Collections - College of Natural Sciences > Department of Chemistry > 1. Journal Articles
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