Nitrofluorene derivatives trapped within MWCNTs for electrocatalysis of NADH: Substituent effects on π-π stacking interaction strength

被引:4
|
作者
Urzua, J. [1 ]
Yanez, C. [1 ]
Carbajo, J. [2 ]
Mozo, J. D. [2 ]
Squella, J. A. [1 ]
机构
[1] Univ Chile, Fac Ciencias Quim & Farmaceut, Ctr Invest Proc Redox CIPRex, Santiago, Chile
[2] Univ Huelva, Dept Electroquim Aplicada, Ctr Invest Cient Tecnol Huelva, Huelva, Spain
关键词
Nitrofluorene derivatives; MWCNT; NADH; Carbon nanotube; Catalytic; Electrooxidation; WALLED CARBON NANOTUBES; SIDEWALL FUNCTIONALIZATION; FLUORENONE DERIVATIVES; OXIDATION; ACID;
D O I
10.1016/j.elecom.2020.106852
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We describe nanostructured electrode platforms composed of multiwalled carbon nanotube/glassy carbon electrodes (MWCNT/GCEs) with entrapped nitroaromatic compounds such as 2-nitrofluorene (2-NF), 2-nitro-9-fluorenone (2-NFN), 2,7-dinitrofluorene (2,7-NF) and 2,7-dinitro-9-fluorenone (2,7-NFN). All of the above nitroaromatic compounds were tested as precursors for the production of redox mediator couples useful for NADH electrocatalysis. In this communication, we reveal the effect of the substituents on both the pi-pi stacking interaction strength and the electrocatalysis of NADH. The results show that the nitro group plays a triple role: it acts as a precursor of the mediator redox couple for NADH electrocatalysis; it increases the pi-pi stacking interaction with the electrode; and it acts as an electron acceptor substituent that promotes the electrocatalysis of NADH.
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页数:7
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