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

• Published in: Electrochemistry communications Vol. 121; p. 106852
• Main Authors: Urzúa, J., Yañez, C., Carbajo, J., Mozo, J.D., Squella, J.A.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01-12-2020; Elsevier
• Subjects: Carbon nanotube; Catalytic; Electrooxidation; MWCNT; NADH; Nitrofluorene derivatives; Carbon nanotube; Electrooxidation; Catalytic; MWCNT; NADH; Nitrofluorene derivatives
• ISSN: 1388-2481; 1873-1902
• DOI: 10.1016/j.elecom.2020.106852

[Display omitted]
•A nanostructured interface containing MWCNT and nitrofluorenes was developed.•All nitrofluorenes are precursors of redox mediator couples NHOH/NO.•The electrocatalytic effect can be tuned by varying the precursor’s substituents.•The effect of the precursor’s substituents on the π-π stacking interaction was studied.•The effect of substituents of nitrofluorenes on NADH electrocatalysis was determined.
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 π-π 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 π-π stacking interaction with the electrode; and it acts as an electron acceptor substituent that promotes the electrocatalysis of NADH.