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dc.contributor.author | Saidani, N. | es_ES |
dc.contributor.author | Morallón, Emilia | es_ES |
dc.contributor.author | Huerta, Francisco | es_ES |
dc.contributor.author | Besbes-Hentati, Salma | es_ES |
dc.contributor.author | Montilla-Jiménez, Francisco | es_ES |
dc.date.accessioned | 2020-10-22T03:32:03Z | |
dc.date.available | 2020-10-22T03:32:03Z | |
dc.date.issued | 2020-07-10 | es_ES |
dc.identifier.issn | 0013-4686 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/152800 | |
dc.description.abstract | [EN] A set of fluoro-functionalized polyaniline conducting polymers was synthesized by cyclic scanning of the potential from acidic solutions containing aniline and 2-fluoroaniline monomers. The monomer feed ratio was varied to modulate the composition of the synthesized materials. The fluorination level of the copolymers was quantified from X-ray photoelectron spectroscopy. The upper inversion potential of the cyclic scans was proved as a suitable tool to tune the fluorination level, as the reactivity of the growing chains depends strongly on that experimental parameter. We found that terminal fluorinated anilines present a reactivity for homocoupling 5 times lower than for heterocoupling, independently of the limiting potential. Conversely, aniline terminal groups present a reactivity strongly dependent on the limiting potential, favoring the heterocoupling reactions at high inversion potentials. The maximum fluorination level of polyaniline rings achieved is about 75%. (C) 2020 Elsevier Ltd. All rights reserved. | es_ES |
dc.description.sponsorship | The authors wish to thank Generalitat Valenciana (PROMETEO/2018/087) for financial support. Nesrine Saidani would like to thank the Tunisian Ministry of Higher Education and Research for funding her stay at the University of Alicante. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | Elsevier | es_ES |
dc.relation.ispartof | Electrochimica Acta | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | Conducting polymers | es_ES |
dc.subject | Electrochemical copolymerization | es_ES |
dc.subject | Fluoroaniline | es_ES |
dc.subject | Monomer reactivity | es_ES |
dc.subject.classification | QUIMICA FISICA | es_ES |
dc.title | Electrochemical synthesis of fluorinated polyanilines | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1016/j.electacta.2020.136329 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/GVA//PROMETEO%2F2018%2F087/ES/Materiales nanoestructurados en análisis químico: Nuevas estrategias de preparación de la muestra basadas en (micro)extracción en fase sólida y desarrollo de nuevos sensores electroquímicos y espectroelectroquímicos/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//MAT2016-76595-R/ES/NUEVAS ESTRATEGIAS DE FUNCIONALIZACION ELECTROQUIMICA DE MATERIALES CARBONOSOS NANOESTRUCTURADOS PARA LA REDUCCION DE OXIGENO Y BIOSENSORES/ | es_ES |
dc.rights.accessRights | Cerrado | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Ingeniería Textil y Papelera - Departament d'Enginyeria Tèxtil i Paperera | es_ES |
dc.description.bibliographicCitation | Saidani, N.; Morallón, E.; Huerta, F.; Besbes-Hentati, S.; Montilla-Jiménez, F. (2020). Electrochemical synthesis of fluorinated polyanilines. Electrochimica Acta. 348:1-8. https://doi.org/10.1016/j.electacta.2020.136329 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1016/j.electacta.2020.136329 | es_ES |
dc.description.upvformatpinicio | 1 | es_ES |
dc.description.upvformatpfin | 8 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 348 | es_ES |
dc.relation.pasarela | S\414842 | es_ES |
dc.contributor.funder | Generalitat Valenciana | es_ES |
dc.contributor.funder | Ministerio de Economía y Competitividad | es_ES |
dc.contributor.funder | Ministère de l'Enseignement Supérieur et de la Recherche Scientifique, Túnez | es_ES |