Four new sodium uranyl borates, α-Na[(UO 2 ) 2 B 10 O 15 (OH) 5 )] ( NaUBO-1 ), β-Na[(UO 2 ) 2 B 10 O 15 (OH) 5 ] ( NaUBO-2 ), Na[(UO 2 ) 2 B 10 O 15 (OH) 5 ]·3H 2 O ( NaUBO-3 ), and Na[(UO 2 )B 6 O 10 (OH)]·2H 2 O ( NaUBO-4 ), and four new thallium uranyl borates, α-Tl 2 [(UO 2 ) 2 B 11 O 18 (OH) 3 ] ( TlUBO-1 ), β-Tl 2 [(UO 2 ) 2 B 11 O 18 (OH) 3 ] ( TlUBO-2 ), Tl[(UO 2 ) 2 B 10 O 16 (OH) 3 ] ( TlUBO-3 ), and Tl 2 [(UO 2 ) 2 B 11 O 19 (OH)] ( TlUBO-4 ), have been prepared via the reaction of sodium nitrate or thallium nitrate, uranyl nitrate, and excess boric acid at 190 °C. These compounds share a common structural motif consisting of a linear uranyl, UO 2 2+, cation surrounded by BO 3 triangles and BO 4 tetrahedra to create a UO 8 hexagonal bipyramidal environment around uranium. The borate anions bridge between uranyl units to create sheets. Additional BO 3 triangles extend from the polyborate layers and are directed approximately perpendicular to the sheets. In some compounds, these units can link the layers together to yield three-dimensional networks with large pores to house the Na + or Tl + cations and water molecules. The structures are all noncentrosymmetric and are either polar or chiral. While the uranyl borate layers are noncentrosymmetric in and of themselves, there is also twisting of the interlayer BO 3 groups to reduce the interlayer spacing, producing helical features in some structures. Na[(UO 2 )B 6 O 10 (OH)]·2H 2 O and β-Tl 2 [(UO 2 ) 2 B 11 O 18 (OH) 3 ], which can be obtained as pure phases, display second-harmonic generation of 532 nm light from 1064 nm light.
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Wang et al. (2010) studied this question.
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