Uranyl triazolate formation via an in situ Huisgen 1,3-dipolar cycloaddition reaction

被引:21
|
作者
Knope, Karah E. [1 ]
Cahill, Christopher L. [1 ]
机构
[1] George Washington Univ, Dept Chem, Washington, DC 20052 USA
来源
CRYSTENGCOMM | 2011年 / 13卷 / 01期
基金
美国国家科学基金会;
关键词
COORDINATION POLYMERS; HYDROTHERMAL CHEMISTRY; LIGAND SYNTHESIS; CLICK CHEMISTRY; FRAMEWORK; HYDROLYSIS; COMPLEXES; URANIUM; ACID;
D O I
10.1039/c0ce00231c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A two dimensional UO22+ coordination polymer, (UO2)(3)(C10H5N3O4)(2)(OH)(2)(H2O)(2), has been synthesized under solvothermal conditions. The triazolate ligand, 1-(4-carboxyphenyl)-1H-1,2,3-triazole-4-carboxylic acid (CPTAZ) has been generated via a 1,3-dipolar cycloaddition of 4-azidobenzoic acid and propiolic acid. Reactions of the UO22+ cation with both the in situ generated triazolate ligand and the presynthesized ligand have been explored. The structure, fluorescent and thermal behaviour of this material are presented, as is a discussion of the utility of in situ ligand formation versus direct assembly.
引用
收藏
页码:153 / 157
页数:5
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