Charging of Self-Doped Poly(Anilineboronic Acid) Films Studied by in Situ ESR/UV/Vis/NIR Spectroelectrochemistry and ex Situ FTIR Spectroscopy

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F11%3A00377567" target="_blank" >RIV/61388955:_____/11:00377567 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1002/cphc.201100567" target="_blank" >http://dx.doi.org/10.1002/cphc.201100567</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1002/cphc.201100567" target="_blank" >10.1002/cphc.201100567</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Charging of Self-Doped Poly(Anilineboronic Acid) Films Studied by in Situ ESR/UV/Vis/NIR Spectroelectrochemistry and ex Situ FTIR Spectroscopy

Popis výsledku v původním jazyce

Polyaniline (PANI) is among the most studied conducting polymers because of its outstanding properties, such as a relatively high conductivity, easy preparation and processing, low cost, and environmental stability.[1] The role of the chemical structuresof PANI in their different varieties?from linear structures to phenazines components?has been followed in detail in recent studies[2, 3] using the powerful in situ ESR/UV/Vis/NIR spectroelectrochmistry[4] and in situ FTIR spectroelectrochemistry.[ 5] Afurther route to vary the chemical structure of PANI is the development of self-doped derivates of PANI which present better solubility,[6] redox activity[7] and conductivity[6, 8] over a wider pH range as compared to PANI. These derivatives contain anionic functional groups which are able to interact with the positively charged nitrogen atoms of the polyaniline chains causing new effects different from those of polymers doped with solution anions. Among the group of self-doped PANI, pol

Název v anglickém jazyce

Charging of Self-Doped Poly(Anilineboronic Acid) Films Studied by in Situ ESR/UV/Vis/NIR Spectroelectrochemistry and ex Situ FTIR Spectroscopy

Popis výsledku anglicky

Polyaniline (PANI) is among the most studied conducting polymers because of its outstanding properties, such as a relatively high conductivity, easy preparation and processing, low cost, and environmental stability.[1] The role of the chemical structuresof PANI in their different varieties?from linear structures to phenazines components?has been followed in detail in recent studies[2, 3] using the powerful in situ ESR/UV/Vis/NIR spectroelectrochmistry[4] and in situ FTIR spectroelectrochemistry.[ 5] Afurther route to vary the chemical structure of PANI is the development of self-doped derivates of PANI which present better solubility,[6] redox activity[7] and conductivity[6, 8] over a wider pH range as compared to PANI. These derivatives contain anionic functional groups which are able to interact with the positively charged nitrogen atoms of the polyaniline chains causing new effects different from those of polymers doped with solution anions. Among the group of self-doped PANI, pol

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CG - Elektrochemie

OECD FORD obor

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Projekt

<a href="/cs/project/GC203%2F07%2FJ067" target="_blank" >GC203/07/J067: Elektronické interakce SWCNT a vodivých polymerů v kompozitech nanotuby/polymer</a><br>

Návaznosti

Z - Vyzkumny zamer (s odkazem do CEZ)

Rok uplatnění

2011

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

ChemPhysChem

ISSN

1439-4235

e-ISSN

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Svazek periodika

12

Číslo periodika v rámci svazku

16

Stát vydavatele periodika

DE - Spolková republika Německo

Počet stran výsledku

5

Strana od-do

2920-2924

Kód UT WoS článku

000297017900010

EID výsledku v databázi Scopus

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