화학공학소재연구정보센터
Inorganic Chemistry, Vol.45, No.20, 8251-8257, 2006
Structural polarity induced by cooperative hydrogen bonding and lone-pair alignment in the molecular uranyl iodate Na-2[UO2(IO3)(4)(H2O)]
Na-2[UO2(IO3)(4)(H2O)] has been synthesized under mild hydrothermal conditions. Its structure consists of Na+ cations and [UO2(IO3)(4)(H2O)](2-) anions. The [UO2(IO3)(4)(H2O)](2-) anions are formed from the coordination of a nearly linear uranyl, UO22+, cation by four monodentate IO3- anions and a coordinating water molecule to yield a pentagonal bipyramidal environment around the uranium center. The water molecules form intermolecular hydrogen bonds with the terminal oxo atoms of neighboring [UO2(IO3)(4)(H2O)](2-) anions to yield one-dimensional chains that extend down the b axis. There are two crystallographically unique iodate anions in the structure of Na-2[UO2(IO3)(4)(H2O)]. One of these anions is aligned so that the lone-pair of electrons is also directed along the b axis. The overall structure is therefore polar, owing to the cooperative alignment of both the hydrogen bonds and the lone-pair of electrons on iodate. The polarity of the monoclinic space group C2 (a = 11.3810(12) angstrom, b = 8.0547(8) angstrom, c = 7.6515(8) angstrom, beta = 90.102(2)degrees Z = 2, T = 193 K) found for this compound is consistent with the structure. Second-harmonic generation of 532 nm light from a 1064 nm laser source yields a response of approximately 16x alpha-SiO2.