Physico-chemical characterization of ferrocenyl-modified hyperbranched poly(ethylenimine) self-assembled multilayers
Author
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Bracamonte, María V.
Author
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Yáñez Soto, Claudia
es_CL
Author
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Bollo Dragnic, Soledad
es_CL
Author
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Rivas, Gustavo A.
es_CL
Author
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Ferreyra, Nancy F.
es_CL
Admission date
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2014-12-17T14:21:03Z
Available date
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2014-12-17T14:21:03Z
Publication date
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2014
Cita de ítem
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Journal of Electroanalytical Chemistry 712 (2014) 124–131
en_US
Identifier
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dx.doi.org/10.1016/j.jelechem.2013.11.018
Identifier
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https://repositorio.uchile.cl/handle/2250/121910
General note
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Artículo de publicación ISI
en_US
Abstract
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In this work, we characterize the electrochemical behavior of a new ferrocenyl-modified, hyperbranched
poly(ethylenimine) (HBPei-Fc). The effects of the ionic strength, pH and the nature of the anion of the
supporting electrolyte on the electrochemical behavior of the redox polymer were studied using cyclic
voltammetry and an electrochemical quartz crystal microbalance. The interactions of the polymer with
the anions of the supporting electrolyte, which was incorporated during the redox process, determined
the electrochemical behavior that was observed. The polymer was employed for the construction of
layer-by-layer-assembled multi-composite films using thiolated gold surfaces with HBPei-Fc as the polycation
and citrate-stabilized gold nanoparticles or glucose oxidase (GOx) as the negative polyelectrolyte.
The self-assembled multilayers were characterized using UV–Vis spectrophotometry and electrochemical
techniques to follow the signal of the ferrocene groups of the polymer. The adsorption of the polymer and
GOx was analyzed using surface plasmon resonance to determine the surface coverage and the kinetic
properties of the process. The results demonstrated that the ferrocenyl-modified polymer is an efficient
platform for the immobilization of both inorganic materials, such as metallic nanoparticles, and
biomolecules.
en_US
Patrocinador
dc.description.sponsorship
The authors thank CONICET, SECyT-UNC and Agencia Nacional
de Promoción Científica y Tecnológica (ANPCYT) and FONDECYT
for the financial support. M.V. Bracamonte thanks CONICET for
the fellowship.