Optical and electrochemical properties of soluble N-hexylcarbazole-co-3,4-ethylenedioxythiophene copolymers

被引:25
作者
Beouch, L
Van, FT
Stephan, O
Vial, JC
Chevrot, C
机构
[1] Univ Cergy Pontoise, Equip React Interfaces, EA 2528, Lab Polymeres & Mat Electroact, F-95013 Cergy Pontoise, France
[2] Univ Grenoble 1, Spectrometrie Phys Lab, F-38402 St Martin Dheres, France
[3] CNRS, UMR C5588, F-38402 St Martin Dheres, France
关键词
D O I
10.1016/S0379-6779(00)00401-X
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We synthesised soluble N-hexylcarbazoie-co-3,4-ethylenedioxythiophene (HCz-co-EDOT) copolymers from mixtures in various ratio of the two corresponding dihalogenated monomers. From EDOT-HCz starting molar ratio: 0.25, 1,4, we obtained random copolymers named, respectively, C1, C2 and C3 and we compared their properties to the two homopolymers synthesised in the same way. The Infra red studies clearly indicated, as expected, that an increase in the amount of ethylenedioxythiophene in the feed composition leads to an increase of the proportion of the corresponding comonomer in the final materials. Elemental analysis point out that the reactivity of dibrominated EDOT seems slightly lower than that of dibrominated HCz. Thin films of copolymer have been prepared and their electrochemical response have been investigated. Absorption and luminescence of these materials have been also studied in CHCl3. Copolymers mainly composed of one monomer (C1 and C3) behaves like the corresponding homopolymers. On an other hand, copolymer (C2) obtained from an equimolar amount of each monomer in the feed composition clearly exhibits distinct signals in optical spectra and in electrochemical behaviour, probably due to the presence of each monomer unit short segments. So, the use of C2 has been explored for possible application in light emitting devices indicating that the p-doping of the material would be facilitated leading to an improved hole injecting when compared to carbazoles homopolymer. It could be particularly interesting as a hole transporting layer in multilayer organic light emitting devices. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:351 / 358
页数:8
相关论文
共 50 条
[41]   Synthesis and polymerization of new monomers derived from 3,4-ethylenedioxythiophene [J].
Schottland, P ;
Stephan, O ;
Le Gall, PY ;
Chevrot, C .
JOURNAL DE CHIMIE PHYSIQUE ET DE PHYSICO-CHIMIE BIOLOGIQUE, 1998, 95 (06) :1258-1261
[42]   CHAIN-LENGTH EFFECT ON THE ELECTROACTIVITY OF POLY(N-ALKYL-3,6-CARBAZOLEDIYL) THIN-FILMS [J].
SIOVE, A ;
ADES, D ;
NGBILO, E ;
CHEVROT, C .
SYNTHETIC METALS, 1990, 38 (03) :331-340
[43]  
SIOVE A, 1989, MAKROMOL CHEM, V190, P1361
[44]   Multiply colored electrochromic carbazole-based polymers [J].
Sotzing, GA ;
Reddinger, JL ;
Katritzky, AR ;
Soloducho, J ;
Musgrave, R ;
Reynolds, JR ;
Steel, PJ .
CHEMISTRY OF MATERIALS, 1997, 9 (07) :1578-1587
[45]   Blue light electroluminescent devices based on a copolymer derived from fluorene and carbazole [J].
Stéphan, O ;
Vial, JC .
SYNTHETIC METALS, 1999, 106 (02) :115-119
[46]   Electrochemical behaviour of 3,4-ethylenedioxythiophene functionalized by a sulphonate group. Application to the preparation of poly(3,4-ethylenedioxythiophene) having permanent cation-exchange properties [J].
Stephan, O ;
Schottland, P ;
Le Gall, PY ;
Chevrot, C ;
Mariet, C ;
Carrier, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 443 (02) :217-226
[47]   SYNTHESIS OF AROMATIC POLY(ETHER KETONE)S BY NICKEL-CATALYZED COUPLING POLYMERIZATION OF AROMATIC DICHLORIDES [J].
UEDA, M ;
ICHIKAWA, F .
MACROMOLECULES, 1990, 23 (04) :926-930
[48]  
VAN FT, IN PRESS SYNTH MET
[49]  
Wellinghoff S. T., 1983, Journal de Physique Colloque, V44, P677, DOI 10.1051/jphyscol:19833132
[50]   STABILITY OF POLYPYRROLE AND POLY(3,4-ETHYLENEDIOXYTHIOPHENE) FOR BIOSENSOR APPLICATION [J].
YAMATO, H ;
OHWA, M ;
WERNET, W .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1995, 397 (1-2) :163-170