Nitrofluorene derivatives trapped within MWCNTs for electrocatalysis of NADH: Substituent effects on pi-pi stacking interaction strength
Author
dc.contributor.author
Urzúa, J.
Author
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Yañez, C.
Author
dc.contributor.author
Carbajo, J.
Author
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Mozo, J. D.
Author
dc.contributor.author
Squella Serrano, Juan
Admission date
dc.date.accessioned
2021-08-23T23:13:56Z
Available date
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2021-08-23T23:13:56Z
Publication date
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2020
Cita de ítem
dc.identifier.citation
Electrochemistry Communications 121 (2020) 106852
es_ES
Identifier
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10.1016/j.elecom.2020.106852
Identifier
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https://repositorio.uchile.cl/handle/2250/181422
Abstract
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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.
es_ES
Patrocinador
dc.description.sponsorship
Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)
CONICYT FONDECYT 1170054
1210899