Construction of hydrophilic N, O-rich carboxylated triazine-covalent organic frameworks for the application in selective simultaneous electrochemical detection
[Display omitted] •Constructed a triazine-COFs with high surface area via a simple method.•Developed a hydrophilic N, O- rich carboxylated triazine-COFs.•Fabricated a novel sensor combining the merits of AuNPs and the designed COFs.•The sensor was highly selective in the simultaneous determination o...
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| Published in | Applied surface science Vol. 545; p. 149047 |
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| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Elsevier B.V
15.04.2021
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| Subjects | |
| Online Access | Get full text |
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| Abstract | [Display omitted]
•Constructed a triazine-COFs with high surface area via a simple method.•Developed a hydrophilic N, O- rich carboxylated triazine-COFs.•Fabricated a novel sensor combining the merits of AuNPs and the designed COFs.•The sensor was highly selective in the simultaneous determination of GA and UA.
In this study, we strategically designed a hydrophilic N, O-rich carboxylated triazine- covalent organic frameworks (ACOF-TaTp) for the application in selective simultaneous electrochemical detection of mixed chemical compounds with closing oxidation potentials. The ACOF-TaTp was firstly constructed with high surface area and hydrophilicity by 2,4,6-tris(4-aminophenyl)-1,3,5-triazine and 1,3,5-triformylphloroglucinol followed with carboxylation by sodium chloroacetate. Characterizations demonstrated the high surface area and rich N, O-electron donors of ACOF-TaTp facilitated the high dispersion and immobilization of AuNPs on it via electrostatic interactions. Based on their chemical properties, Gallic acid (GA) and uric acid (UA) were selected as model compounds for the test and the result showed their closing oxidation peaks could be clearly separated by ACOF-TaTp, which could be ascribed to its high surface area and stronger affinity to GA than to UA via H-bonding. The constructed sensor AuNPs@ ACOF-TaTp/GCE exhibited high selectivity and sensitivity in the simultaneous determination of GA and UA with a wide linear response in the range of 1–175 μM for GA and 1–150 μM for UA and detection limit of 0.19 μM and 0.25 μM respectively. This work paves a way for strategical design of functionalized COFs for simultaneous electrochemical sensing. |
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| AbstractList | [Display omitted]
•Constructed a triazine-COFs with high surface area via a simple method.•Developed a hydrophilic N, O- rich carboxylated triazine-COFs.•Fabricated a novel sensor combining the merits of AuNPs and the designed COFs.•The sensor was highly selective in the simultaneous determination of GA and UA.
In this study, we strategically designed a hydrophilic N, O-rich carboxylated triazine- covalent organic frameworks (ACOF-TaTp) for the application in selective simultaneous electrochemical detection of mixed chemical compounds with closing oxidation potentials. The ACOF-TaTp was firstly constructed with high surface area and hydrophilicity by 2,4,6-tris(4-aminophenyl)-1,3,5-triazine and 1,3,5-triformylphloroglucinol followed with carboxylation by sodium chloroacetate. Characterizations demonstrated the high surface area and rich N, O-electron donors of ACOF-TaTp facilitated the high dispersion and immobilization of AuNPs on it via electrostatic interactions. Based on their chemical properties, Gallic acid (GA) and uric acid (UA) were selected as model compounds for the test and the result showed their closing oxidation peaks could be clearly separated by ACOF-TaTp, which could be ascribed to its high surface area and stronger affinity to GA than to UA via H-bonding. The constructed sensor AuNPs@ ACOF-TaTp/GCE exhibited high selectivity and sensitivity in the simultaneous determination of GA and UA with a wide linear response in the range of 1–175 μM for GA and 1–150 μM for UA and detection limit of 0.19 μM and 0.25 μM respectively. This work paves a way for strategical design of functionalized COFs for simultaneous electrochemical sensing. |
| ArticleNumber | 149047 |
| Author | He, Yasan Deng, Yanhua Chen, Jianhua Lin, Xiaogeng Hu, Shirong |
| Author_xml | – sequence: 1 givenname: Xiaogeng surname: Lin fullname: Lin, Xiaogeng organization: College of Chemistry, Chemical Engineering and Environment, Minnan Normal University, Zhangzhou 363000, PR China – sequence: 2 givenname: Yanhua surname: Deng fullname: Deng, Yanhua organization: College of Chemistry, Chemical Engineering and Environment, Minnan Normal University, Zhangzhou 363000, PR China – sequence: 3 givenname: Yasan surname: He fullname: He, Yasan email: 2319578008@qq.com organization: College of Chemistry, Chemical Engineering and Environment, Minnan Normal University, Zhangzhou 363000, PR China – sequence: 4 givenname: Jianhua surname: Chen fullname: Chen, Jianhua email: jhchen73@126.com organization: College of Chemistry, Chemical Engineering and Environment, Minnan Normal University, Zhangzhou 363000, PR China – sequence: 5 givenname: Shirong surname: Hu fullname: Hu, Shirong organization: College of Chemistry, Chemical Engineering and Environment, Minnan Normal University, Zhangzhou 363000, PR China |
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•Constructed a triazine-COFs with high surface area via a simple method.•Developed a hydrophilic N, O- rich carboxylated... |
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| SubjectTerms | Carboxylation Covalent organic frameworks Gallic acid Gold nanoparticles Uric acid |
| Title | Construction of hydrophilic N, O-rich carboxylated triazine-covalent organic frameworks for the application in selective simultaneous electrochemical detection |
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