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Growth of N-substituted polypyrrole layers in ionic liquids: Synthesis and its electrochromic properties

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dc.creator Ahmad, Shahzada
dc.creator Kazim, Samrana
dc.creator Uygun, Aysegul
dc.creator ŞEN GÜRSOY, SONGÜL
dc.date 2012-03-31T21:00:00Z
dc.date.accessioned 2020-10-06T10:32:50Z
dc.date.available 2020-10-06T10:32:50Z
dc.identifier 77a036b6-bd44-4181-aebe-dbdcfb5d2132
dc.identifier 10.1016/j.solmat.2011.09.049
dc.identifier https://avesis.sdu.edu.tr/publication/details/77a036b6-bd44-4181-aebe-dbdcfb5d2132/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/63843
dc.description A new series of pyrrole family, N-substituted phenyl attached alkyl at the ortho, meta and para position were synthesized by a straight forward method and were exploited as an innovative monomer for electroactive polymers. Ionic liquids were employed as a medium for electro-polymerization of these monomers to obtain N-(methyl)phenyl polypyrroles. N-substituted polypyrroles show different morphologies and conductivity according to position of methyl group on the benzene ring and synthesis medium. The electrical conductivity value varies with the position of methyl group and was > 10(-5) S/cm, higher than the sample obtained from conventional media. The resulting polymer films were characterized by Fr-IR and UV-Vis spectroscopy, contact angle measurements, cyclic voltammetry and scanning probe microscopic technique along with their electrochromic behavior. (C) 2011 Elsevier B.V. All rights reserved.
dc.language eng
dc.rights info:eu-repo/semantics/openAccess
dc.title Growth of N-substituted polypyrrole layers in ionic liquids: Synthesis and its electrochromic properties
dc.type info:eu-repo/semantics/article


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