請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/61001完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 劉貴生(Guey-Sheng Liou) | |
| dc.contributor.author | Ya-Wen Chuang | en |
| dc.contributor.author | 莊雅雯 | zh_TW |
| dc.date.accessioned | 2021-06-16T10:40:45Z | - |
| dc.date.available | 2018-08-01 | |
| dc.date.copyright | 2013-08-28 | |
| dc.date.issued | 2013 | |
| dc.date.submitted | 2013-08-13 | |
| dc.identifier.citation | Chapter 1
1. Lee, H.; Neville, K. Handbook of Epoxy Resins, McGraw-Hill, New York 1967. 2. Pascault, J. P.; Williams, R. J. J. Epoxy Polymers-New Materials and Innovations, Wiley-VCH 2010. 3. Huang, K. Y.; Shiu, C. L.; Wu, P.S.; Wei, Y.; Yeh, J. M.; Li, W. T. Electrochim. Acta 2009, 54, 5400. 4. Huang, T. C.; Su, Y. A.; Yeh, T. C.; Huang, H. Y.; Wu, C. P.; Huang, K. Y.; Chou, Y. C.; Yeh, J. M.; Wei, Y. Electrochim. Acta 2011, 56, 6142. 5. Yang, T. I.; Peng, C. W.; Lin, Y. L.; Weng, C. J.; Edgington, G.; Mylonakis, A.; Huang, T. C.; Hsu, C. H.; Yeh, J. M.; Wei, Y. J. Mater. Chem. 2012, 22, 15845. 6. Yang, X. J.; Jiang, Y. b.; Zhao, T.; Yu, Y. Z. J. Appl. Polym. Sci. 2006, 102, 1071. 7. Jeng, R. J.; Wang J. R.; Lin, J. J.; Liu, Y. L.; Chiu, Y. S.; Su, W. C. J. Appl. Polym. Sci. 2001, 82, 3526. 8. Bilyeu, B.; Brostow, W.; Menard, K. P. J. Mater. Ed. 1999, 21, 281. 9. Monk, P. M. S.; Mortimer, R. J.; Rosseinsky, D. R. Electrochromism: Fundamentals and Applications; VCH, Weinheim, Germany 1995. 10. Platt, J. R. J. Chem. Phys. 1961, 34, 862. 11. Byker, H. Proc. Electrochem. Soc. 1994, 94-2, 3. 12. (a) Deb, S. K. Appl. Opt., Suppl. 1969, 3, 192. (b) Deb, S. K. Philos. Mag. 1973, 27, 801. 13. (a) Lampert, C. M. Sol. Energy Mater. 1984, 11, 1. (b) Green, M. Chem. Ind. 1996, 17, 641. (c) Kubo, T.; Tanimoto, J.; Minami, M.; Toya, T.; Nishikitani, Y.; Watanabe, H. Solid State Ionics 2003, 165, 97. (d) Lee, E. S.; DiBartolomeo D. L. Sol. Energy Mater. Sol. Cells 2002, 71, 465. (e) Bach, U.; Corr, D.; Lupo, D.; Pichot, F.; Ryan, M. Adv. Mater. 2002, 14, 845. 14. Dautremont-Smith, W. C. Displays 1982, 3, 3. 15. de Tacconi, N. R.; Rajeshwar, K.; Lezna, R. O. Chem. Mater. 2003, 15, 3046. 16. Monk, P. M. S.; Mortimer, R. J.; Rosseinsky, D. R. Electrochromism and Electrochromic Devices; Cambridge University Press: Cambridge, UK 2007. 17. Bange, K.; Bambke, T. Adv. Mater. 1990, 2, 10. 18. Mortimer, R. J. Electrochim. Acta. 1999, 44, 2971. 19. Mortimer, R. J.; Dyer, A. L.; Reynolds, J. R. Displays 2006, 27, 2. 20. Deb, S. K. Appl. Optics. suppl. 1969, 3, 192. 21. Faughnan, B. W.; Crandall, R. S. in Pankove (ed.), J. I. Devices, Springer Verlang, Berlin, 1980, Chapter 5. 22. Granqvist, G. V. Phys. Thin Films 1993, 17, 301. 23. (a) Gottesfeld, S.; McIntyre J. D. E.; Beni, G.; Shay, J. L. Appl. Phys. Lett. 1978, 33, 208. (b) Gottesfeld, S.; McIntyre, J. D. E. J. Electrochem. Soc. 1979, 126, 742. 24. Monk, P. M. S.; Man, C. M. J. Mater. Sci. 1999, 10, 101. 25. (a) Beni, G.; Rice, C. E.; Shay, J. L. J. Electrochem. Soc. 1980, 127, 1342. (b) Kang, K. S.; Shay, J. L. J. Electrochem. Soc. 1983, 130, 766. (c) Beni, G.; Shay, J. L. Appl. Phys. Lett. 1978, 33, 567. 26. Mortimer, R. J. Chem. Soc. Rev. 1997, 26, 147. 27. Neff, V. D. J. Electrochem. Soc. 1978, 125, 886. 28. (a) Itaya K.; Uchida I.; Neff V. D. Acc. Chem. Res. 1986, 19, 162. (b) Tacconi, N. R.; Rajeshwar, K.; Lezna, R. O. Chem. Mater. 2003, 15, 3046. 29. Collins, G. C. S.; Schiffrin, D. J. J. Electrochem. Soc. 1985, 132, 1835. 30. Mastragostino, M.; Arbizzani, C.; Bongini, A.; Barbarella, G.; Zambianchi, M. Electrochim. Acta. 1993, 38, 135. 31. Dyer, A. L.; Craig, M. R.; Babiarz, J. E.; Kiyak, K.; Reynolds, J. R. Macromolecules 2010, 43, 4460. 32. (a) Sapp, S. A.; Sotzing, G. A.; Reynolds, J. R. Chem. Mater. 1998, 10, 2101. (b) Kumar, A.; Welsh, D. M.; Morvant, M. C.; Piroux, F.; Abboud, K. A.; Reynolds, J. R. Chem. Mater. 1998, 10, 896. (c) Sonmez, G.; Sonmez, H. B.; Shen, C. K. F.; Wudl, F. Adv. Mater. 2004, 16, 1905. 33. (a) Thompson, B. C.; Schottland, P.; Zong, K.; Reynolds, J. R. Chem. Mater. 2000, 12, 1563. (b) Thompson, B. C.; Schottland, P.; Sonmez, G.; Reynolds, J. R. Synth. Met. 2001, 119, 333. (c) Schwendeman, I.; Hickman, R.; Sonmez, G.; Schottland, P.; Zong, K.; Welsh, D.; Reynolds, J. R. Chem. Mater. 2002, 14, 3118. 34. (a) Sonmez, G.; Shen, C. K. F.; Rubin, Y.; Wudl, F. Angew. Chem. Int. Ed. 2004, 43, 1498. (b) Sonmez, G. Chem. Commun. 2005, 5251. (c) Sonmez, G.; Shen, C. K. F.; Rubin, Y.; Wudl, F. Adv. Mater. 2005, 17, 897. (d) Sonmez, G.; Schwendeman, I.; Schottland, P.; Zong, K.; Reynolds, J. R. Macromolecules 2003, 36, 639. (e) Skotheim, T. A.; Elsenbaumer, R. L.; Reynolds, J. R. Handbook of Conducting Polymers, Marcel Dekker, New York, 2nd edn, 1998. (f) Nalwa, H. S. Handbook of Organic Conductive Molecules and Polymers, John Wiley & Sons, New York 1997. 35. (a) Oishi, Y; Ishida, M.; Kakimoto, M. A.; Imai, Y.; Kurosaki, T. J. Polym. Sci., Part A: Polym. Chem. 1992, 30, 1027. (b) Liou, G. S.; Hsiao, S. H.; Ishida, M.; Kakimoto, M. A.; Imai, Y. J. Polym. Sci., Part A: Polym. Chem. 2002, 40, 3815. (c) Leung, M. K.; Chou, M. Y.; Su, Y. O.; Chiang, C. L.; Chen, H. L.; Yang, C. F.; Yang, C. C.; Lin, C. C.; Chen, H. T. Org. Lett. 2003, 5, 839. 36. (a) Chou, M. Y.; Leung, M. K.; Su, Y. O.; Chiang, C. L.; Lin, C. C.; Liu, J. H.; Kuo, C. K.; Mou, C. Y. Chem. Mater. 2004, 16, 654. (b) Otero, L.; Sereno, L.; Fungo, F.; Liao, Y. L.; Lin, C. Y.; Wong, K. T. Chem. Mater. 2006, 18, 3495. (c) Natera, J.; Otero, L.; Sereno, L.; Fungo, F.; Wang, N. S.; Tsai, Y. M.; Hwu, T. Y.; Wong, K. T. Macromolecules 2007, 40, 4456. (d) Natera, J.; Otero, L.; D’Eramo, F.; Sereno, L.; Fungo, F.; Wang, N. S.; Tsai, Y. M.; Wong, K. T. Macromolecules 2009, 42, 626. (e) Yang, C. H.; Liu, F. J.; Huang, L. R.; Wang, T. L.; Lin, W. C.; Sato, M.; Chen, C. H.; Chang, C. C. J. Electroanal. Chem. 2008, 617, 101. (f) Koyuncu, F. B.; Koyuncu, S.; Ozdemir, E. Electrochim. Acta 2010, 55, 4935. (g) Ramirez, C. L.; Parise, A. R. Org. Electron. 2009, 10, 747. (h) Koyuncu, S.; Gultekin, B.; Zafer, C.; Bilgili, H.; Can, M.; Demic, S.; Kaya, I.; Icli, S. Electrochim. Acta 2009, 54, 5694. 37. Beaupre’, S.; Dumas, J.; Leclerc, M. Chem. Mater. 2006, 18, 4011. 38. Lim, B.; Nah, Y. C.; Hwang, J. T.; Ghim, J.; Vak, D.; Yun, J. M.; Kim, D. Y. J. Mater. Chem. 2009, 19, 2380. 39. (a) Su, T. H.; Hsiao, S. H.; Liou, G. S. J. Polym. Sci. Part A: Polym. Chem. 2005, 43, 2085. (b) Cheng, S. H.; Hsiao, S. H.; Su, T. H.; Liou, G. S. Macromolecules 2005, 38, 307. 40. (a) Liou, G. S.; Hsiao, S. H.; Su, T. H. J. Mater. Chem. 2005, 15, 1812. (b) Liou, G. S.; Hsiao, S. H.; Huang, N. K.; Yang, Y. L. Macromolecules 2006, 39, 5337. (c) Chang, C. W.; Liou, G. S.; J. Mater. Chem. 2008, 18, 5638. (d) Chang, C. W.; Chung, C. H.; Liou, G. S. Macromolecules 2008, 41, 8441. (e) Liou, G. S.; Lin, H. Y.; Yen, H. J. J. Mater. Chem. 2009, 19, 7666. (f) Liou, G. S.; Lin, H. Y. Macromolecules 2009, 42, 125. 41. (a) Yen, H. J.; Liou, G. S. J. Polym. Sci. Part A: Polym. Chem. 2009, 47, 1584. (b) Huang, L. T.; Yen, H. J.; Chang, C. W.; Liou, G. S. J. Polym. Sci. Part A: Polym. Chem. 2010, 48, 4747. (c) Yen, H. J.; Liou, G. S. Org. Electron. 2010, 11, 299. 42. (a) Liou, G. S.; Hsiao, S. H.; Chen, W. C.; Yen, H. J. Macromolecules 2006, 39, 6036. (b) Liou, G. S.; Yen, H. J. J. Polym. Sci. Part A: Polym. Chem. 2006, 44, 6094. (c) Chang, C. W.; Liou, G. S.; Hsiao, S. H. J. Mater. Chem. 2007, 17, 1007. (d) Yen, H. J.; Liou, G. S. J. Mater. Chem. 2010, 20, 9886. 43. (a) Liou, G. S.; Hsiao, S. H.; Chen, H. W. J. Mater. Chem. 2006, 16, 1831. (b) Liou, G. S.; Chen, H. W.; Yen, H. J. J. Polym. Sci. Part A: Polym. Chem. 2006, 44, 4108. (c) Liou, G. S.; Chen, H. W.; Yen, H. J. Macromol. Chem. Phys. 2006, 207, 1589. (d) Liou, G. S.; Chang, C. W.; Huang, H. M.; Hsiao, S. H. J. Polym. Sci. Part A: Polym. Chem. 2007, 45, 2004. (e) Chang, C. W.; Yen, H. J.; Huang, K. Y.; Yeh, J. M.; Liou, G. S. J. Polym. Sci. Part A: Polym. Chem. 2008, 46, 7937. (f) Liou, G. S.; Chang, C. W. Macromolecules 2008, 41, 1667. (g) Hsiao, S. H.; Liou, G. S.; Kung, Y. C.; Yen, H. J. Macromolecules 2008, 41, 2800. (h) Yen, H. J.; Liou, G. S. Chem. Mater. 2009, 21, 4062. 44. Yen, H. J.; Lin, K. Y.; Liou, G. S. J. Mater. Chem. 2011, 21, 6230. 45. D’Alessandro, D. M.; Keene, F. R. Chem. Soc. Rev. 2006, 35, 424. 46. (a) Hush, N. S. Prog. Inorg. Chem. 1967, 8, 391. (b) Hush, N. S. Electrochim. Acta 1968, 13, 1005. 47. (a) Hush, N. S. Prog. Inorg. Chem. 1967, 8, 391. (b) Hush, N. S. Electrochim. Acta 1968, 13, 1005. 48. (a) Brunschwig, B. S.; Creutz, C.; Sutin, N. Chem. Soc. Rev. 2002, 31, 168. (b) Brunschwig, B. S.; Sutin, N. Coord. Chem. Rev. 1999, 187, 233. (c) Robin, M. B.; Day, P. Adv. Inorg. Chem. Radiochem. 1967, 10, 247. 49. (a) Creutz, C. Prog. Inorg. Chem. 1983, 30, 1. (b) Richardson, D. E.; Taube, H. Coord. Chem. Rev. 1984, 60, 107. 50. (a) Kalyanasundaram, K.; Nazeeruddin, M. K. Inorg. Chim. Acta. 1994, 226, 213. (b) Ward, M. D. Chem. Soc. Rev. 1995, 24, 121. 51. Nelsen, S. F. Chem. Eur. J. 2000, 6, 581. 52. Welsh, D. M.; Kumar, A.; Meijer, E. W.; Reynolds, J. R. Adv. Mater. 1999, 11, 1379. 53. (a) Sassi, M.; Salamone, M. M.; Ruffo, R.; Mari, C. M.; Pagani, G. A.; Beverina, L. Adv. Mater. 2012, 24, 2004. (b) Gao, L. P.; Ding, G. J.; Wang, Y. C.; Yang, Y. L. Appl. surf. sci. 2011, 258, 1184. 54. Rakotomalala, M.; Wagner, S.; Doring, M. Materials 2010, 3, 4300. 55. (a) Seo, E. T.; Nelson, R. F.; Fritsch, J. M.; Marcoux, L. S.; Leedy, D. W.; Adams, R. N. J. Am. Chem. Soc. 1966, 88, 3498. (b) Nelson, R. R.; Adams, R. N. J. Am. Chem. Soc. 1968, 90, 3925. 56. (a) Ogino, K.; Kanegae, A.; Yamaguchi, R.; Sato, H.; Kurjata, J. Macromol. Rapid Commmun. 1999, 20, 103. (b) Yu, W. L.; Pei, J.; Huang, W.; Heeger, A. J. Chem. Commun. 2000, 8, 681. (c) Chou, M. Y.; Leung, M. K.; Su, Y. O.; Chiang, C. L.; Lin, C. C.; Liu, J. H.; Kuo, C. K.; Mou, C. Y. Chem. Mater. 2004, 16, 654. 57. (a) Lin, H. Y.; Liou, G. S. Macromolecules, 2009, 42, 125. (b) Yen, H. J.; Liou, G. S. Org. Electron. 2010, 11, 299. (c) Huang, L. T.; Yen, H. J.; Liou, G. S. Macromolecules 2011, 44, 9595. (d) Yen, H. J.; Lin, H. Y.; Liou, G. S. Chem. Mater. 2011, 23, 1874. (e) Huang, L. T.; Yen, H. J.; Wu, J. H.; Liou, G. S. Org. Electron. 2012, 13, 840. (f) Yen, H. J.; Lin, K. Y.; Liou, G. S. J. Polym. Sci. Part A Polym. Chem. 2012, 50, 61. Chapter 2 1. (a) Chang, C. W.; Liou, G. S.; Hsiao, S. H. J. Mater. Chem. 2007, 17, 1007. (b) Yen, H. J.; Liou, G. S. Chem. Mater. 2009, 21, 4062. (c) Yen, H. J.; Lin, K. Y.; Liou, G. S. J. Mater. Chem. 2011, 21, 6230. 2. Monk, P. M. S.; Mortimer, R. J.; Rosseinsky, D. R. Electrochromism and Electrochromic Devices; Cambridge University Press: New York 2007. 3. (a) Bach, U.; Corr, D.; Lupo, D.; Pichot, F.; Ryan, M. Adv. Mater. 2002, 14, 845. (b) Ma, C.; Taya, M.; Xu, C. Polym. Eng. Sci. 2008, 48, 2224. (c) Beaupre, S.; Breton, A. C.; Dumas, J.; Leclerc, M. Chem. Mater., 2009, 21, 1504. 4. (a) Rose, T. L.; D’Antonio, S.; Jillson, M. H.; Kon, A. B.; Suresh, R.; Wang, F. Synth. Met. 1997, 85, 1439. (b)Franke, E. B.; Trimble, C. L.; Hale, J. S.; Schubert, M.; Woollam, J. A. J. Appl. Phys. 2000, 88, 5777. (c) Topart, P.; Hourquebie, P. Thin Solid Films 1999, 352, 243. (d) Chandrasekhar, P. ; Zay, B. J.; McQueeney, T.; Scara, A.; Ross, D.; Birur, G. C.; Haapanen, S.; Kauder, L.; Swanson, T.; Douglas, D. Synth. Met. 2003, 23, 135. 5. (a) Vickers, S. J.; Ward, M. D. Electrochem. Commun. 2005, 7, 389. (b) Schwab, P. F. H.; Diegoli, S.; Biancardo, M.; Bignozzi, C. A. Inorg. Chem. 2003, 42, 6613. (c) Qi, Y.; Wang, Z. Y. Macromolecules 2003, 36, 3146. (d) Wang, S.; Todd, E. K.; Birau, M.; Zhang, J.; Wan, X.; Wang, Z. Y. Chem. Mater. 2005, 17, 6388. (e) Zheng, J.; Qiao, W.; Wan, X.; Gao, J. P.; Wang, Z. Y. Chem. Mater. 2008, 20, 6163. (f) Hasanain, F.; Wang, Z. Y. Dyes Pigm. 2009, 83, 95. (g) Shi, P.; Amb, C. M.; Knott, E. P.; Thompson, E. J.; Liu, D. Y.; Mei, J.; Dyer, A. L.; Reynolds, J. R. Adv. Mater. 2010, 22, 4949. (h) Sonmez, G.; Meng, H.; Zhang, Q.; Wudl, F. Adv. Funct. Mater. 2003, 13, 726. (i) Sonmez, G.; Meng, H.; Wudl, F. Chem. Mater. 2004, 16, 574. (j) Li, M.; Patra, A.; Sheynin, Y.; Bendikov, M. Adv. Mater. 2009, 21, 1707. 6. (a) Seo, E. T.; Nelson, R. F.; Fritsch, J. M.; Marcoux, L. S.; Leedy, D. W.; Adams, R. N. J. Am. Chem. Soc. 1966, 88, 3498. (b) Nelson, R. F.; Adams, R. N. J. Am. Chem. Soc. 1968, 90, 3925. 7. (a) Ito, A.; Ino, H.; Tanaka, K.; Kanemoto, K.; Kato, T. J. Org. Chem. 2002, 67, 491. (b) Chiu, K. Y.; Su, T. H.; Li, J. H.; Lin, T. H.; Liou, G. S.; Cheng, S. H. J. Electroanal. Chem. 2005, 575, 95. 8. (a) Creutz, C.; Taube, H. J. Am .Chem. Soc. 1973, 95, 1086. (b) Lambert, C.; Noll, G. J. Am. Chem. Soc. 1999, 121, 8434. 9. Robin, M.; Day, P. Adv. Inorg. Radiochem. 1967, 10, 247. 10. Szeghalmi, A. V.; Erdmann, M.; Engel, V.; Schmitt, M.; Amthor, S.; Kriegisch, V.; Noll, G.; Stahl, R.; Lambert, C.; Leusser, D.; Stalke, D.; Zabel, M.; Popp, J. J. Am. Chem. Soc. 2004, 126, 7834. 11. (a) Chang, C. W.; Liou, G. S. J. Mater. Chem. 2008, 18, 5638. (b) Huang, L. T.; Yen, H. J.; Liou, G. S. J. Polym. Sci. Part A: Polym. Chem. 2010, 48, 4747. (c) Yen, H. J.; Lin, H. Y.; Liou, G. S. Chem. Mater. 2011, 23, 1874. (d) Huang, L. T.; Yen, H. J.; Liou, G. S. Macromolecules 2011, 44, 9595. (e) Yen, H. J.; Liou, G. S. Polym. Chem. 2012, 3, 255. (f) Huang, L. T.; Yen, H. J.; Wu, J. H.; Liou, G. S. Org. Electron. 2012, 13, 840. (g) Yen, H. J.; Chen, C. J.; Liou, G. S. Adv. Funct. Mater. 2013, DOI: 10.1002/adfm.201300569. 12. Lee, H.; Neville, K. Handbook of Epoxy Resins, McGraw-Hill, New York 1967. 13. (a) Sassi, M.; Salamone, M. M.; Ruffo, R.; Mari, C. M.; Pagani, G. A.; Beverina, L. Adv. Mater. 2012, 24, 2004. (b) Gao, L. P.; Ding, G. J.; Wang, Y. C.; Yang, Y. L. Appl. surf. sci. 2011, 258, 1184. 14. Rakotomalala, M.; Wagner, S.; Doring, M. Materials 2010, 3, 4300. 15. Bard, A. J.; Faulkner, L. R. Electrochemical Methods: Fundamentals and Applications, Wiley: New York 2001. Chapter 3 1. Lee, H.; Neville, K. Handbook of Epoxy Resins, McGraw-Hill, New York 1967. 2. Monk, P. M. S.; Mortimer, R. J.; Rosseinsky, D. R. Electrochromism: Fundamentals and Applications; VCH, Weinheim, Germany 1995. 3. Dautremont-Smith, W. C. Displays 1982, 3, 3. 4. de Tacconi, N. R.; Rajeshwar, K.; Lezna, R. O. Chem. Mater. 2003, 15, 3046. 5. Monk, P. M. S.; Mortimer, R. J.; Rosseinsky, D. R. Electrochromism and Electrochromic Devices; Cambridge University Press: Cambridge, UK 2007. 6. Bange, K.; Bambke, T. Adv. Mater. 1990, 2, 10. 7. Mortimer, R. J. Electrochim. Acta. 1999, 44, 2971. 8. Mortimer, R. J.; Dyer, A. L.; Reynolds, J. R. Displays 2006, 27, 2. 9. (a) Cheng, S. H.; Hsiao, S. H.; Su, T. H.; Liou, G. S. Macromolecules 2005, 38, 307. (b) Su, T. H.; Hsiao, S. H.; Liou, G. S. J. Polym. Sci. Part A: Polym. Chem. 2005, 43, 2085. (c) Liou, G. S.; Chang, C. W. Macromolecules 2008, 41, 1667. (d) Hsiao, S. H.; Liou, G. S.; Kung, Y. C.; Yen, H. J. Macromolecules 2008, 41, 2800. (e) Chang, C. W.; Chung, C. H.; Liou, G. S. Macromolecules 2008, 41, 8441. (f) Chang, C. W.; Liou, G. S. J. Mater. Chem. 2008, 18, 5638. (g) Chang, C. W.; Yen, H. J.; Huang, K. Y.; Yeh, J. M.; Liou, G. S. J. Polym. Sci. Part A: Polym. Chem. 2008, 46, 7937. (h) Hsiao, S. H.; Liou, G. S.; Wang, H. M. J. Polym. Sci. Part A: Polym. Chem. 2009, 47, 2330. (i) Liou, G. S.; Lin, H. Y.; Yen, H. J. J. Mater. Chem. 2009, 19, 7666. (j) Huang, L. T.; Yen, H. J.; Liou, G. S. J. Polym. Sci. Part A: Polym. Chem. 2010, 48, 4747. (k) Yen, H. J.; Lin, H. Y.; Liou, G. S. Chem. Mater. 2011, 23, 1874. (l) Huang, L. T.; Yen, H. J.; Liou, G. S. Macromolecules 2011, 44, 9595. (m) Yen, H. J.; Liou, G. S. Polym. Chem. 2012, 3, 255. (n) Huang, L. T.; Yen, H. J.; Wu, J. H.; Liou, G. S. Org. Electron. 2012, 13, 840. (o) Yen, H. J.; Chen, C. J.; Liou, G. S. Adv. Funct. Mater. 2013, DOI: 10.1002/adfm.201300569. 10. (a) Chang, C. W.; Liou, G. S.; Hsiao, S. H. J. Mater. Chem. 2007, 17, 1007. (b) Yen, H. J.; Liou, G. S. Chem. Mater. 2009, 21, 4062. | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/61001 | - |
| dc.description.abstract | 本研究所使用的三種二胺單體4,4'-diamino-4'-methoxytriphenylamine, N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine和 N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-4,4'-biphenyldiamine在本實驗室之前發表的文獻中已合成過。本論文分為四個章節,第一章為總體序論。第二章包含了以4,4'-diamino-4'-methoxytriphenylamine, N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine和 N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-4,4'-biphenyldiamine為主體與diglycidyl ether bisphenol A經由熱硬化合成出一系列新型的熱固性電致變色環氧樹脂。第三章包含了以4,4'-diamino-4'-methoxytriphenylamine和N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine為主體與脂肪族環氧樹脂triglycidyl isocyanurate 經由熱硬化合成出一系列新型的熱固型色淡電致變色環氧樹脂。第四章為結論。這四個系列新型三苯胺取代衍生之熱固型環氧樹脂之合成與基本特性、電化學及電致變色性質已被研究與比較。所有的熱固型環氧樹脂皆有好的玻璃轉移溫度、出色的熱穩定性及機械性質。在利用電化學與光譜電化學的方法下,大部分的熱固型環氧樹脂也展現很好且可逆的電致變色特性。相較於三苯胺對應的聚醯胺,導入三苯胺衍生物進入環氧樹脂可有效的增加氧化的階段及呈現多段電致變色的性質。此外,由於脂肪族的環氧樹脂含有較剛硬的結構,故相較於芳香族的環氧樹脂表現出較高的玻璃轉移溫度。直至目前為止,以三苯胺結構之二胺當作交聯劑,合成出具三苯胺之電致變色熱固性環氧樹脂,尚未被製備並且系統化探討,故本研究開創了一個環氧樹脂的新的應用領域。 | zh_TW |
| dc.description.abstract | The three diamines which were used in this research, 4,4'-diamino-4'-methoxytriphenylamine, N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine, and N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-4,4'-biphenyldiamine, were published by our group before. This study has been separated into four chapters. Chapter 1 is general introduction. Chapter 2 includes a series of novel electrochromic thermoset epoxy resins based on 4,4'-diamino-4'-methoxytriphenylamine, N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine and N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-4,4'-biphenyldiamine, and diglycidyl ether bisphenol A via curing reaction. The chapter 3 include a series of novel electrochromic aliphatic-typed thermoset epoxy resins and derived from 4,4'-diamino-4'-methoxytriphenylamine and N,N'-bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine, and triglycidyl isocyanurate by curing reaction. Chapter 4 is conclusions. The synthesis, thermal properties, electrochemical and electrochromic properties of four series of novel aromatic triphenylamine (TPA)-substituted derived thermoset epoxy resins were investigated and compared. All thermoset epoxy resins had good high Ts values, good thermal stability, and mechanical properties. Most of the obtained epoxy resins also revealed excellent reversibility of electrochromic characteristics by the electrochemical and spectroelectrochemical methods. Comparing with corresponding polyamides, introduction of triarylamine derivatives into epoxy resins could effectively increase the oxidation stages and reveal multielectrochrmic behaviors. Besides, comparing with aromatic-typed epoxy resins, due to its rigid structure and highly crosslinking density, the aliphatic-typed thermoset epoxy resins showed much higher Ts values than aromatic-typed. To the best of our knowledge, the TPA-based electrochromic thermoset epoxy materials derived from diamines with triarylamine structures as curing agent have not been prepared and investigated systemically. This study opens a new world of application in epoxy resins. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-16T10:40:45Z (GMT). No. of bitstreams: 1 ntu-102-R00549008-1.pdf: 3652318 bytes, checksum: 3c114147daf68ef3daf3797ef5639fee (MD5) Previous issue date: 2013 | en |
| dc.description.tableofcontents | CHAPTER 1
General Introduction 1.1 EPOXY RESINS 2 1.1.1 General Introduction of Epoxy Resins 2 1.1.2 Manufacturing of Epoxy Resins 3 1.1.3 Hardeners 4 1.1.4 Applications 5 1.2 INTRODUCTION OF ELECTROCHROMISM 7 1.2.1 Evolution of Electrochromism 7 1.2.2 Electrochromic Systems 10 1.2.2.1 Transition-metal Oxides 11 Tungsten Trioxide (WO3) 11 Iridium Oxide (IrO2) 12 1.2.2.2 Coordination Complexes 12 Prussian Blue (PB) 12 Phthalocyanines (Pc) 13 1.2.2.3 Organic Molecules 14 Viologens 14 1.2.2.4 Conducting Polymers 15 1.2.2.5 Arylamine-based Polymers 17 1.3 INTERVALENCE-CHARGE TRANSFER (IV-CT) 21 1.3.1 Theoretical Background 22 1.3.2 Classification of Mixed-valence Compounds 24 1.3.3 Optically-induced Transition 24 1.3.4 Thermally-induced Transition 25 1.3.5 Electrochemical Methods and the Comproportionation Equilibrium 26 1.3.6 Predictions for the IV-CT Band Shape 27 1.4 RESEARCH MOTIVATION 28 REFERENCES AND NOTES 30 CHAPTER 2 IV-CT Characterizations of Novel Electrochromic Diglycidyl Ether Bisphenol A Cured with Triphenylamine-based Derivatives ABSTRACT OF CHAPTER 2 37 2.1 INTRODUCTION 38 2.2 EXPERIMENTAL SECTION 41 2.2.1 Materials 41 2.2.2 Preparation of the Thermoset Epoxy Thick Films 42 4,4'-Diamino-4'-methoxytriphenylamine/DGEBA Thick Film 42 N,N'-Bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine/DGEBA Thick Film 42 N,N'-Bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-4,4'-biphenyldiamine/DGEBA Thick Film 42 2.2.3 Preparation of the Thermoset Epoxy Resin Thin Films 43 4,4'-Diamino-4'-methoxytriphenylamine/DGEBA Thin Film 43 N,N'-Bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine/DGEBA Thin Film 43 N,N'-Bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-4,4'-biphenyldiamine/DGEBA Thin Film 44 2.2.4 Measurements 44 2.3 RESULTS AND DISCUSSION 46 2.3.1 Thermoset Epoxy Resins Synthesis 46 2.3.2 Thermoset Epoxy Properties 47 Basic Characterization 47 Electrochemical Properties 51 Measurement of n-Electrons Transfered for Thermoset Epoxy IIb 54 Spectroelectrochemistry and Electrochromic Properties 57 2.4 SUMMARY 65 REFERENCES AND NOTES 66 CHAPTER 3 Synthesis and Characterizations of Colorless Electrochromic Devices Based on Aliphatic Epoxy Cured with Triphenylamine-based Derivatives ABSTRACT OF CHAPTER 3 69 3.1 INTRODUCTION 70 3.2 EXPERIMENTAL SECTION 72 3.2.1 Materials 72 3.2.2 Preparation of the Thermoset Epoxy Resin Thick Films 73 4,4'-diamino-4'-methoxytriphenylamine /TGIC Thick Film 73 N,N'-Bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine/TGIC Thick Film 73 3.2.3 Preparation of the Thermoset Epoxy Resin Thin Films 73 4,4'-Diamino-4'-methoxytriphenylamine/TGIC Thin Film 73 N,N'-Bis(4-aminophenyl)-N,N'-di(4-methoxylphenyl)-1,4-phenylenediamine/TGIC Thin Film 74 3.2.4 Measurements 74 3.3 RESULTS AND DISCUSSION 76 3.3.1 Thermoset Epoxy Resins Synthesis 76 3.3.2 Polymer Properties 77 Basic Characterization 77 Spectroelectrochemistry and Electrochromic Properties 84 REFERENCES AND NOTES 92 | |
| dc.language.iso | en | |
| dc.subject | 三苯胺 | zh_TW |
| dc.subject | 環氧樹脂 | zh_TW |
| dc.subject | 電致變色 | zh_TW |
| dc.subject | 價間電子傳導 | zh_TW |
| dc.subject | 色淡 | zh_TW |
| dc.subject | electrochromism | en |
| dc.subject | triphenylamine | en |
| dc.subject | epoxy | en |
| dc.subject | colorless | en |
| dc.subject | intervalence-charge transfer (IV-CT) | en |
| dc.title | 新型具三苯胺衍生物之熱固性環氧樹脂合成與電致變色特性之研究 | zh_TW |
| dc.title | Synthesis and Electrochromism of Novel Thermoset Epoxy Materials Containing Triphenylamine Derivatives | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 101-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 蕭勝輝(Sheng-Huei Hsiao),陳燿騰(Yaw-Terng Chern),呂奇明(Chyi-Ming Leu),龔宇睿(Yu-Ruei Kung) | |
| dc.subject.keyword | 三苯胺,環氧樹脂,電致變色,價間電子傳導,色淡, | zh_TW |
| dc.subject.keyword | triphenylamine,epoxy,electrochromism,intervalence-charge transfer (IV-CT),colorless, | en |
| dc.relation.page | 115 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2013-08-13 | |
| dc.contributor.author-college | 工學院 | zh_TW |
| dc.contributor.author-dept | 高分子科學與工程學研究所 | zh_TW |
| 顯示於系所單位: | 高分子科學與工程學研究所 | |
文件中的檔案:
| 檔案 | 大小 | 格式 | |
|---|---|---|---|
| ntu-102-1.pdf 未授權公開取用 | 3.57 MB | Adobe PDF |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。
