Six-Fold Coordinated Uranyl Cations in Extended Coordination Polymers

被引:74
|
作者
Mihalcea, Ionut [1 ]
Henry, Natacha [1 ]
Bousquet, Till [1 ]
Volkringer, Christophe [1 ]
Loiseau, Thierry [1 ]
机构
[1] Univ Lille Nord France, Contribut Unite Catalyse & Chim Solide UCCS, CNRS, ENSCL,UMR 8181, F-59652 Villeneuve Dascq, France
关键词
METAL-ORGANIC FRAMEWORK; CRYSTAL-STRUCTURE; HYDROTHERMAL SYNTHESIS; TETRAOXIDO CORE; URANIUM; LIGAND; ION; COMPLEXATION; MINERALS; GEOMETRY;
D O I
10.1021/cg300853f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Four uranyl-organic framework-type compounds have been hydrothermally synthesized with different ditopic aromatic dicarboxylates. The use of 1,4-benzenedicarboxylate (noted 1,4-bdc), 4,4'-biphenyldicarboxylate (noted 4,4'-bpdc), 4,4'-azobenzenedicarboxylate (noted 4,4'-adc), and 1,3-benzenedicarboxylate (noted 1,3-bdc) gave rise to the crystallization of a series of phases UO2(L) (L = 1,4-bdc (1), 4,4'-bpdc (2), 4,4'-adc (3), or 1,3-bdc (4)), which exhibited 6-fold coordinated uranyl centers as monomeric square bipyramidal unit. The crystal structures showed that the para position of the carboxylate groups favored the formation of layered extended assemblies in 1-3, whereas the meta isomer isophthalate induced the formation of a three-dimensional framework. In situ X-ray diffraction of the thermal behavior indicated the decomposition of the different networks in the range 360-420 degrees C, successively followed by the crystallization of the uranium oxide U3O8.
引用
收藏
页码:4641 / 4648
页数:8
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