In Situ Ligand Formation-Driven Synthesis of a Uranyl Organic Framework as a Turn-on Fluorescent pH Sensor

被引:40
作者
Gu, Dongxu [1 ]
Yang, Weiting [1 ]
Ning, Guohua [1 ]
Wang, Fuxiang [1 ]
Wu, Shuixing [1 ]
Shi, Xiaodong [2 ]
Wang, Yinghui [3 ]
Pan, Qinhe [1 ]
机构
[1] Hainan Univ, Haikou, Hainan, Peoples R China
[2] Univ S Florida, Tampa, FL 33620 USA
[3] Chinese Acad Sci, Changchun Inst Appl Chem, Changchun, Peoples R China
基金
中国国家自然科学基金;
关键词
INTRAMOLECULAR PROTON-TRANSFER; HYDROTHERMAL SYNTHESIS; COORDINATION POLYMERS; CRYSTAL-STRUCTURE; COMPLEX; MOF; HYDROXYLATION; STRATEGY; TERTIARY; SERIES;
D O I
10.1021/acs.inorgchem.9b02999
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A uranium-based metal-organic framework, [(UO2)(H(2)DTATC)] (HNU-39, H(4)DTAT C = 5,5 ' -( 9,10- dihydroxy-4a,9,9 a,10-tetrahydroanthracene-9,1 0- diyl) - diisophthalic acid) was successfully prepared by a hydrothermal method. The structure of HNU-39 comprises UO8 hexagonal bipyramids linked by doubly protonated DTATC ligands, forming a ribbon arrangement. It is worth noting that the DTATC ligand was transformed in situ from 5,5'-(anthracene-9,10-diyl)diisophthalic acid (H(4)DPATC) during the synthesis of HNU-39. Research on fluorescence properties has shown that HNU-39 exhibits fluorescence turn-on response under alkaline conditions and could be used as a potential pH sensor. Moreover, HNU-39 can also be successfully applied for pH sensing in real samples from a sewage treatment plant. The sensing mechanism can be interpreted as OH - ions reacting with the protons in the organic ligand of HNU-39.
引用
收藏
页码:1778 / 1784
页数:7
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