Electroactive multifunctional telechelic stairs-shaped poly(bicarbazyl-alkylene)s
| dc.rights.license | open | |
| hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
| dc.contributor.author | CLOUTET, Eric
IDREF: 151048681 | |
| dc.contributor.author | YAMMINE, P. | |
| dc.contributor.author | ADÈS, D. | |
| dc.contributor.author | SIOVE, A. | |
| dc.date.accessioned | 2020 | |
| dc.date.available | 2020 | |
| dc.date.issued | 1999 | |
| dc.identifier.issn | 0379-6779 | |
| dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/19585 | |
| dc.description.abstractEn | Chemical oxidation of α,ω-bis(N-carbazolyl)alkanes by FeCl3 in the presence of N-(ω-functional alkyl)carbazoles allowed the obtention of telechelic stairs-shaped poly(bicarbazyl-alkylene)s bearing terminal groups such as halogens, nitrile, carboxylic acid. High molar masses materials were obtained exhibiting a particularly good solubility in organic solvents due to their special architecture. Electrochemical studies disclosed that redox polymers were obtained displaying a remarkable colourlessgreenblue electrochromism. Furthermore materials could be used as a blue lightemitting layer into diodes. | |
| dc.language.iso | en | |
| dc.publisher | Elsevier | |
| dc.title.en | Electroactive multifunctional telechelic stairs-shaped poly(bicarbazyl-alkylene)s | |
| dc.type | Article de revue | |
| dc.identifier.doi | 10.1016/S0379-6779(98)00983-7 | |
| dc.subject.hal | Chimie/Polymères | |
| bordeaux.journal | Synthetic Metals | |
| bordeaux.page | 1302-1303 | |
| bordeaux.volume | 102 | |
| bordeaux.hal.laboratories | Laboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629 | * |
| bordeaux.issue | 1-3 | |
| bordeaux.institution | Bordeaux INP | |
| bordeaux.institution | Université de Bordeaux | |
| bordeaux.peerReviewed | oui | |
| hal.identifier | hal-02930389 | |
| hal.version | 1 | |
| hal.origin.link | https://hal.archives-ouvertes.fr//hal-02930389v1 | |
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