Electrochromic linear and star branched poly(3,4-ethylenedioxythiophene-didodecyloxybenzene) polymers

被引:94
作者
Wang, F
Wilson, MS
Rauh, RD
Schottland, P
Thompson, BC
Reynolds, JR
机构
[1] EIC Labs Inc, Norwood, MA 02062 USA
[2] Univ Florida, Dept Chem, Ctr Macromol Sci & Engn, Gainesville, FL 32611 USA
关键词
D O I
10.1021/ma9918506
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
New linear and star structured poly(3,4-ethylenedioxythiophene-didodecyloxybezenes) (PEBs) have been prepared which exhibit thermochromism and multicolor electrochromism as they are able to produce the three basic colors in the RGB system: red, green, and blue. The star polymer features a conjugated hyperbranched poly(triphenylamine) core with FEB arms ca. 8-10 repeat units (16-20 rings) in length. Red in solution, the optical spectra of both polymers exhibit a maximum absorption at 455 nm in the neutral state. Linear and star FEB are thermally stable up to 300 degrees C as demonstrated by TGA. The presence of an EDOT-phenylene repeat in the conjugated backbone results in a relatively low half-wave potential of + 0.20 V vs Fc/Fc(+), which is lower than regioregular poly(3-hexylthiophene) by 0.4 V and only slightly higher than PEDOT. As a result, star FEB is the first representative of a new class of star-shaped polymers where it is possible to address the electroactive arms independently from the conjugated core. The redox switching properties of these star PEBs are quite stable with a 90% retention of electroactivity after 4500 double potential switches. These properties are of particular importance for electrochemically based display applications where highly stable processable electrochromic polymers are needed.
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页码:2083 / 2091
页数:9
相关论文
共 25 条
[1]  
C.I.E, 1971, CIE PUBL, V15
[2]   Thermochromic properties of quaterthiophene, an alkyl-substituted quaterthiophene derivative and its corresponding polymer [J].
DiCesare, N ;
Belletete, M ;
Leclerc, M ;
Durocher, G .
CHEMICAL PHYSICS LETTERS, 1998, 291 (5-6) :487-495
[3]   Towards a theoretical design of thermochromic polythiophenes [J].
DiCesare, N ;
Belletete, M ;
Durocher, G ;
Leclerc, M .
CHEMICAL PHYSICS LETTERS, 1997, 275 (5-6) :533-539
[4]   ELECTROCHEMICAL AND SPECTROSCOPIC CHARACTERIZATION OF POLYALKYLENEDIOXYTHIOPHENES [J].
DIETRICH, M ;
HEINZE, J ;
HEYWANG, G ;
JONAS, F .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1994, 369 (1-2) :87-92
[5]   RECOMMENDATIONS ON REPORTING ELECTRODE-POTENTIALS IN NONAQUEOUS SOLVENTS (RECOMMENDATIONS 1983) [J].
GRITZNER, G ;
KUTA, J .
PURE AND APPLIED CHEMISTRY, 1984, 56 (04) :461-466
[6]   Synthesis and characterization of new processible conducting copolymers derived from thiophenes [J].
Hanna, R ;
Leclerc, M .
CHEMISTRY OF MATERIALS, 1996, 8 (07) :1512-1518
[7]   POLY(ALKYLENEDIOXYTHIOPHENE)S - NEW, VERY STABLE CONDUCTING POLYMERS [J].
HEYWANG, G ;
JONAS, F .
ADVANCED MATERIALS, 1992, 4 (02) :116-118
[8]   Low-oxidation-potential conducting polymers: alternating substituted para-phenylene and 3,4-ethylenedioxythiophene repeat units [J].
Irvin, JA ;
Reynolds, JR .
POLYMER, 1998, 39 (11) :2339-2347
[9]   Conducting poly(3,4-alkylenedioxythiophene) derivatives as fast electrochromics with high-contrast ratios [J].
Kumar, A ;
Welsh, DM ;
Morvant, MC ;
Piroux, F ;
Abboud, KA ;
Reynolds, JR .
CHEMISTRY OF MATERIALS, 1998, 10 (03) :896-902
[10]   Chromic phenomena in neutral polythiophene derivatives [J].
Leclerc, M ;
Frechette, M ;
Bergeron, JY ;
Ranger, M ;
Levesque, I ;
Faid, K .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 1996, 197 (07) :2077-2087