Functional decoration on a regenerable bifunctional porous covalent organic framework probe for rapid detection and adsorption of copper ions

被引:0
|
作者
Yu-Long Li [1 ]
Xi-Lang Jin [1 ,2 ]
Yi-Ting Ma [1 ]
Jing-Rui Liu [1 ]
Fazal Raziq [3 ]
Peng-Yuan Zhu [4 ]
Zhi-Feng Deng [5 ]
Hong-Wei Zhou [1 ]
Wei-Xing Chen [1 ]
Wen-Huan Huang [4 ]
机构
[1] School of Materials and Chemical Engineering,Xi'an Technological University
[2] Yulin Boyi-Jingking Research Institute of Industrial Technology Development Research
[3] KAUST Catalysis Center,King Abdullah University of Science and Technology
[4] Key Laboratory of Chemical Additives for China National Light Industry,College of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology
[5] National and Local Joint Engineering Laboratory for Slag Comprehensive Utilization and Environmental Technology, School of Materials Science and Engineering,Shaanxi University of Technology
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
O657.3 [光化学分析法(光谱分析法)];
学科分类号
070302 ; 081704 ;
摘要
Developing fluorescence porous probe for detecting and eliminating Cu2+contamination in water or biosystem is an essential research project that has attracted considerable attention.However,improving the fluorescence detecting efficiency while enhancing the adsorption capacity of the porous probe is of great challenge.Herein,a bifunctional two-dimensional imine-based porous covalent organic framework(TTP-COF) probe was designed and synthesized from 1,3,5-tris(4-aminopheny l) benzene(TAPB) and 2,4,6-Triformylphloroglucinol(TP) ligand.TTP-COF displayed rapid detection of Cu2+(limit of detection(LOD)=10 nmol·L-1while achieving a high adsorption capacity of 214 mg·g-1(pH=6) at room temperature with high reusability(> 5 cycles).The key roles and contributions of high π-conjugate and delocalized electrons in TABP and functional-OH groups in TP were proved.More importantly,the fluorescence quenching mechanism of TTP-COF was studied by density functional theory theoretical calculations,revealing the crucial role of intramolecular hydrogen bonds among C=N and-OH groups and the blocking of the excited state intramolecular proton transfer process in detecting process of Cu2+.
引用
收藏
页码:758 / 769
页数:12
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