Near-Infrared Electrochromism in Electroactive Pentacenediquinone-Containing Poly(aryl ether)s
Source abstract
Abstract
The synthesis and near-infrared electrochromic properties of pentacenediquinone-containing monomers and polymers are reported. The electroactive pentacenediquinone units were incorporated into poly(aryl ether)s in varying degrees by copolymerization. The polymers possessed good thermal stabilities and high glass transition temperatures, and could undergo two reversible steps of electrochemical reduction. Near-infrared electrochromic properties of pentacenediquinone-containing poly(aryl ether)s were studied by spectroelectrochemical analysis, which showed that the radical anions possess intense near-infrared absorption with λ max values between 1331 and 1430 nm, while the dianions also exhibit absorption between 880 and 965 nm. The reduced polymer film displayed intense and broad near-infrared absorption, which was surprisingly stable in air over a long period. The neutral and reduced polymers had electrical conductivity of 1 × 10 - 6 and 3 × 10 - 3 S/cm, respectively.
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Research context
OpenAlex topics: Conducting polymers and applications · Transition Metal Oxide Nanomaterials · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Polymer Science and Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, People's Republic of China, and Department of Chemistry, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario, Canada K1S 5B6
References (38)
Show source-provided references
1. Monk, P. M. S.; Mortimer, R. J.; Rosseinsky, D. R.Electrochromism: Fundamentals and Application; VCH: Weinheim, 1995.10.1002/9783527615377 ↗
2. Argun A. A. · Chem. Mater. · 2004 · 16 · 440110.1021/cm049669l ↗
3. Thompson B. C. · Chem. Mater. · 2000 · 12 · 156310.1021/cm000097o ↗
4. Rosseinsky D. R. · J. Adv. Mater. · 2001 · 13 · 78310.1002/1521-4095(200106)13:11<783::AID-ADMA783>3.0.CO;2-D ↗
5. Rauh R. D. · Electrochim. Acta · 1999 · 44 · 316510.1016/S0013-4686(99)00034-1 ↗
6. Chandrasekhar P. · Synth. Met. · 2001 · 119 · 29310.1016/S0379-6779(00)01455-7 ↗
7. McDongh A. M. · Chem. Mater. · 2000 · 12 · 252310.1021/cm001104b ↗
8. Qi Y. · Macromolecules · 2003 · 36 · 314610.1021/ma021018s ↗
9. Schwendeman I. · Adv. Mater. · 2001 · 13 · 63410.1002/1521-4095(200105)13:9<634::AID-ADMA634>3.0.CO;2-3 ↗
10. Meng H. · Adv. Mater. · 2003 · 15 · 14610.1002/adma.200390030 ↗
11. Rastegar M. F. · Org. Lett. · 2004 · 6 · 451910.1021/ol048021b ↗
12. Wang Z. Y. · Pure Appl. Chem. · 2004 · 76 · 143510.1351/pac200476071435 ↗
13. (c) Desjardins, P.; Wang, Z. Y. InACS Symposium Series; Jenekhe, S. A., Kiserow, D. J., Eds.; ACS−Oxford University Press: DC, 2004; Vol. 888, pp 51−65.
14. Qi Y. H. · Chin. J. Polym. Sci. · 2003 · 21 · 147
15. Qi Y. H. · Opt. Mater. · 2003 · 21 · 25510.1016/S0925-3467(02)00146-5 ↗
16. (f) Qi, Y. H.; Desjardins, P.; Wang, Z. Y.J. Opt.A: Pure Appl. Opt.2002,4, S273.10.1088/1464-4258/4/6/366 ↗
17. Vickers S. J. · Electrochem. Commun. · 2005 · 7 · 38910.1016/j.elecom.2005.02.013 ↗
18. García-Cañadas J. · Angew. Chem., Int. Ed. · 2003 · 42 · 301110.1002/anie.200351338 ↗
19. Schwab P. F. H. · Inorg. Chem. · 2003 · 42 · 661310.1021/ic0346782 ↗
20. Biancardo M. · Collect. Czech. Chem. Commun. · 2003 · 68 · 171010.1135/cccc20031710 ↗
21. Almlof J. E. · J. Am. Chem. Soc. · 1990 · 11210.1021/ja00159a049 ↗
22. Tonzola C. J. · J. Am. Chem. Soc. · 2003 · 125 · 1354810.1021/ja036314e ↗
23. Tonzola C. J. · Macromolecules · 2004 · 37 · 355410.1021/ma035971o ↗
24. Katz H. E. · Acc. Chem. Res. · 2001 · 34 · 35910.1021/ar990114j ↗
25. Jacob J. · J. Am. Chem. Soc. · 2004 · 126 · 698710.1021/ja0398823 ↗
26. Chmil K. H. · Synth. Met. · 1997 · 84 · 38710.1016/S0379-6779(97)80795-3 ↗
27. Xiaoyi P. · Dyes Pigm. · 1993 · 23 · 7910.1016/0143-7208(93)80027-X ↗
28. Tian H. · Mater. Chem. Phys. · 1994 · 36 · 33210.1016/0254-0584(94)90050-7 ↗
29. Jozefiak T. H. · J. Am. Chem. Soc. · 1987 · 109 · 656010.1021/ja00255a078 ↗
30. Rak S. F. · J. Org. Chem. · 1990 · 55 · 479410.1021/jo00303a008 ↗
31. Almlöf J. E. · J. Am. Chem. Soc. · 1990 · 112 · 120610.1021/ja00159a049 ↗
32. Liberko C. A. · J. Am. Chem. Soc. · 1993 · 115 · 247810.1021/ja00059a050 ↗
33. Wang Z. · Dyes Pigm. · 1996 · 30 · 26110.1016/0143-7208(95)00089-5 ↗
34. Mills W. H. · J. Chem. Soc., Trans. · 1912 · 101 · 219410.1039/CT9120102194 ↗
35. Kejecik M. · J. Electroanal. Chem. · 1991 · 317 · 17910.1016/0022-0728(91)85012-E ↗
36. Yamamoto T. · Synth. Met. · 1995 · 69 · 52910.1016/0379-6779(94)02555-D ↗
37. Yamamoto T. · Macromolecules · 1995 · 28 · 337110.1021/ma00113a042 ↗
38. Muramatsu Y. · Chem. Lett. · 1997 · 58110.1246/cl.1997.581 ↗