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Mild Periodic Acid Flux and Hydrothermal Methods for the Synthesis of Crystalline f‑Element-Bearing Iodate Compounds

f-element-bearing iodate compounds are a large family mostly synthesized by hydrothermal reactions starting with actinide/lanthanide ions and iodic acid or iodate salt. In this work, we introduce melting periodic acid flux as a new reaction medium and provide a safe way for single-crystal growth of...

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Bibliographic Details
Published in:Inorganic chemistry 2017-11, Vol.56 (21), p.13041-13050
Main Authors: Wang, Yaxing, Duan, Tao, Weng, Zhehui, Ling, Jie, Yin, Xuemiao, Chen, Lanhua, Sheng, Daopeng, Diwu, Juan, Chai, Zhifang, Liu, Ning, Wang, Shuao
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Language:English
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Summary:f-element-bearing iodate compounds are a large family mostly synthesized by hydrothermal reactions starting with actinide/lanthanide ions and iodic acid or iodate salt. In this work, we introduce melting periodic acid flux as a new reaction medium and provide a safe way for single-crystal growth of a series of new f-element iodate compounds including UO2(IO3)2·H2O (1), UO2(IO3)2(H2O)·HIO3 (2), α-Th­(IO3)2(NO3)­(OH) (3), β-Th­(IO3)2(NO3)­(OH) (4), and (H3O)9Nd9(IO3)36·3HIO3 (5). The structures of these compounds deviate from those afforded from hydrothermal reactions. Specifically, compounds 1 and 2 exhibit pillared structures consisting of uranyl pentagonal bipyramids and iodate trigonal pyramids. Compounds 3 and 4 represent two new thorium iodate compounds that are constructed from subunits of thorium dimers. Compound 5 exhibits a flower-shaped trivalent lanthanide iodate structure with HIO3 molecules and H3O+ cations filled in the channels. The aliovalent replacement of f elements in 5 is available from a hydrothermal process, further generating compounds of Th2(IO3)8(H2O) (6) and Ce2(IO3)8(H2O) (7). The distinct absorption features are observed in isotypic compounds 5–7, where 7 shows typical semiconductor behavior with a band gap of 2.43 eV. Remarkably, noncentrosymmetric 1, 6, and 7 exhibit strong second-harmonic-generation efficiencies of 1.3, 3.2, and 9.2 times, respectively, that of the commercial material KH2PO4. Additionally, the temperature-dependent emission spectra of 1 and 2 were also collected showing typical emission features of uranyl units and a negative correlation between the intensities of the emissions with temperature. Clearly, the presented low-temperature melting inorganic acid flux synthesis would provide a facile and effective strategy to produce a large new family of structurally versatile and multifunctional f-element inorganic compounds.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.7b01855