English
新闻公告
More
化学进展 前一篇   后一篇

• 综述与评论 •

含Silole共轭聚合物的光电性能

刘治田1*, 胡钊1, 沈陟1, 胡双强1, 王子兴2, 戚欣1   

  1. 1. 武汉工程大学材料科学与工程学院 武汉 430074;
    2. 上海大学新型显示技术及应用集成教育部重点实验室 上海 200072
  • 收稿日期:2011-07-01 修回日期:2011-10-01 出版日期:2012-03-24 发布日期:2011-11-25
  • 通讯作者: 刘治田 E-mail:able.ztliu@gmail.com
  • 基金资助:

    国家自然科学基金项目(No.51003080)、湖北省教育厅科学研究计划重点项目(No.D20111502)和新型显示技术及应用集成教育部重点实验室(上海大学)开放基金项目(No.P201002)资助

Optoelectronic Properties of Silole-Containing Polymers

Liu Zhitian1*, Hu Zhao1, Shen Zhi1, Hu Shuangqiang1, Wang Zixing2, Qi Xin1   

  1. 1. School of Materials Science and Engineering, Wuhan Institute of Technology, Wuhan 430074, China;
    2. Key Laboratory for Advanced Displays and System Application, Ministry of Education, Shanghai University, Shanghai 200072, China
  • Received:2011-07-01 Revised:2011-10-01 Online:2012-03-24 Published:2011-11-25
Silole是一类含硅杂环戊二烯,近年来,由于其独特的结构特性、分子的可设计性及多样性,在光电领域得到越来越多研究者们的关注。某些silole小分子在有机发光二极管中用作发光层和电子传输层有出色的表现,但近来对含silole聚合物的研究也颇受重视,在聚集态诱导发光、化学传感器、聚合物发光二极管、聚合物太阳能电池、场效应晶体管中的应用相继有报道。因此silole是一类很有潜力的构筑光电功能材料的杂环化合物。本文根据其母体结构的不同对含silole的聚合物光电性能研究进展进行了综述。
Siloles are a group of five-membered silacyclics, which have drawn much attention due to its unique electronic structures, molecule diversity and designability recently. High performance OLED can be made using small silole molecules as emitting materials or electron transfer materials. Silole-containing polymers have also attracted much attention of a number of chemists. Besides the high conductivity, many new properties have been found, such as highly efficient power conversion efficiency in plastic solar cells, fast carrier mobility in field-effect transistors (FET), high efficiency in polymeric light-emitting diodes (PLEDs), etc. Thus siloles are promising optoelectronic functional materials. In this review, the optoelectronic properties of silole-containing polymers are described according to the different structures of their parent compounds. Contents
1 Introduction
2 Substituted silole
2.1 Poly(1,1-silole)s
2.2 Poly(2,5-silole)s
2.3 Poly(3,4-silole)s
3 Dibenzosilole
4 Dithienosilole
5 Bis-silicon-bridged stilbene
6 Conclusion

中图分类号: 

()
[1] Yamaguchi S, Tamao K. Bull. Chem. Soc. Jpn., 1996, 69 :2327-2334
[2] Tamao K, Uchida M, Izumizawa T, Furukawa K, Yamaguchi S. J.Am. Chem. Soc., 1996, 118: 11974-11975
[3] Colomer E, Corriu R J P, Lheureux M. Chem. Rev., 1990, 90: 265-282
[4] Dubac J, Guerin C, Meunier P. The Chemistry of Organic Silicon Compounds, Vol. 2 (Eds. Rappoport Z, Apeloig Y). John Wiley & Sons, 1999. Chapter 34
[5] Yamaguchi S, Endo T, Uchida M, Izumizawa T, Furukawa K, Tamao K. Chem. Eur. J., 2000, 6: 1683-1692
[6] Sohn H, Huddleston R, Powell D R, West R, Oka K, Xu Y H. J. Am. Chem. Soc., 1999, 121: 2935-2936
[7] Chen J, Peng H, Law C C W, Dong Y, Lam J W Y, Williams I D, Tang B Z. Macromolecules, 2003, 36: 4319-4327
[8] Hermanns J, Schmidt B. J. Chem. Soc. Perkin Trans., 1998, (1): 2209-2230
[9] Wang E G, Li C, Mo Y, Zhang Y, Ma G, Shi W, Peng J B, Yang W, Cao Y. J. Mater. Chem., 2006, 16: 4133-4140
[10] Braye E H, Hubel W. Chem. Ind. (Lond.), 1959, 1250-1251
[11] Chen J W, Cao Y. Macromol. Rapid Commun., 2007, 28: 1714-1742
[12] Chen J W, Cao Y. Accounts of Chemical Research, 2009, 11:1709-1718
[13] Li Z, Dong Y Q, Lam J W Y, Sun J X, Qin A J, Haubler M, Dong Y P, Sung H H Y, Williams H S K, Tang B Z. Adv. Funct. Mater., 2009, 19: 905-917
[14] Murata H, Malliaras G G, Uchida M, Shen Y, Kafafi Z H. Chem. Phys. Lett. 2001, 339, 161-166
[15] Luo J, Xie Z, Lam J W Y, Cheng L, Chen H, Qiu C, Kwok H S, Zhan X, Liu Y, Zhu D, Tang B Z. Chem. Commun., 2001,1740-1741
[16] Li Z, Dong Y Q, Mi B X, Tang Y H, Haussler M, Tong H, Dong Y P, Lam J W Y, Ren Y, Sung H H Y, Wong K S, Gao P, Williams L D, Kwok H S, Tang B Z.J. Phys. Chem. B, 2005, 109: 10061-10066
[17] Hong Y N, Lam J W Y, Tang B Z. Chem. Commun., 2009, (29): 4332-4353
[18] Palilis L C, Makinen A J, Uchida M, Kafafi Z H. Appl. Phys. Lett., 2003, 82(14): 2209-2211
[19] Oshita J, Kai H, Takata A, Iida T, Kunai A, Ohta N, Komaguchi K, Shiotani M, Adachi A, Sakamaki K, Okita K. Organometallics, 2001, 20: 4800-4805
[20] Chen J W, Xu B, Yang K X, Cao Y, Sung H H Y, Williams L D, Tang B Z.J. Phys. Chem. B, 2005,109: 17086-17093
[21] Lee J, Yuan YY, Kang Y J, Jia W L, Lu Z H, Wang S N. Adv. Func. Mater., 2006, 16: 681-686
[22] Tamao K, Yamaguchi S, Shiozaki M, Nakagawa Y, Ito Y. J. Am. Chem. Soc.,1992, 114 : 5867-5869
[23] Chen J, Law C C W, Lam J W Y, Dong Y, Lo S M F, Williams I D, Zhu D, Tang B Z. Chem. Mater., 2003, 15: 1535-1546
[24] Liu Z T, Lei G T, Yu Z B, Yuan W, Pei Q B, Chen J W, Cao Y. PMSE Preprints, 2009, 101: 958-959
[25] Mo Y Q, Tian R Y, Shi W, Cao Y. Chem. Commun., 2005, 4925-4926
[26] Liu M S, Luo J, Jen A K Y. Chem. Mater., 2003,15: 3496-3500
[27] Huo L J, Chen H Y, Hou J H, Chen T L, Yang Y. Chem. Commun, 2009, 5570-5572
[28] Chu T Y, Lu J P, Beaupre S,Zhang Y U, Pouliot J R, Wakim S,Zhou J Y, Leclerc M, Li Z, Ding J F, Tao Y. J.Am. Chem. Soc., 2011, 133(12): 4250-4253
[29] Du X B, Wang Z Y. Chem.Commun., 2011, 47: 4276-4278
[30] Sohn H, Calhoun R W, Sailor M J, Trogler W C. Angew. Chem. Int. Ed., 2001, 40: 2104-2015
[31] Usta H, Lu G, Facchetti A, Marks T J. J. Am. Chem. Soc., 2006, 128: 9034-9035
[32] Yamaguchi S, Jin R Z, Tamao K. J. Am. Chem. Soc., 1999, 121: 2937-2938
[33] Chen J W, Xie Z L, Lam J W K, Law C C W, Tang B Z. Macromolecules, 2003, 36: 1108-1117
[34] Shinar J, Ijadi-Maghsoodi S, Ni Q X, Pang Y, Barton T J. Synth. Met., 1989, 28: 593-598
[35] Barton T J, Ijadi-Maghsoodi S, Pang Y. Macromolecules, 1991, 24: 1257-1260
[36] Tamao K, Yamaguchi S, Shiro M. J. Am. Chem. Soc., 1994,116: 11715-11722
[37] Yamaguchi S, Jin R Z, Itami Y, Goto T, Tamao K. J. Am. Chem. Soc., 1999, 121: 10420-10421
[38] Wang F, Luo J, Yang K S, Chen J W, Huang F, Cao Y. Macromolecules, 2005, 38: 2253-2260
[39] Wang F, Luo J, Chen J W, Huang F, Cao Y. Polymer, 2005, 46: 8422-8429
[40] Wang Y, Hou L T, Yang K X, Chen J W, Wang F, Cao Y. Macromol. Chem. Phys., 2005, 206: 2190-2198
[41] Liu Z T, Wang L, Chen J W, Wang F, Ouyang X Y, Cao Y. J. Polym. Sci. Part A: Polym. Chem., 2007, 45: 756-767
[42] Liu Y Q, Chen Z, Chen J W, Wang F, Cao Y. Polymer Bulletin, 2007, 59: 31-44
[43] Liu Z T, Zou J H, Chen J W, Huang L, Peng J B, Cao Y. Polymer, 2008, 49: 1604-1610
[44] 刘治田(Liu Z T), 邹建华(Zou J H), 陈军武(Chen J W), 刘永强(Liu Y Q), 彭俊彪(Peng J B), 曹镛(Cao Y). 高分子学报(Acta Polymerica Sinica), 2009, 9: 845-851
[45] Horst S, Evans N R, Bronstein H A, Williams C K. J. Polym. Sci. Part A: Polym. Chem., 2009, 47: 5116-5125
[46] Gilman H, Gorsich R D. J. Am. Chem. Soc., 1955, 77: 6380-6381
[47] Chen R F, Fan Q L, Zheng C. Org. Lett., 2006, 8: 203-205
[48] Liu Y, Stringfellow T C, Ballweg D. J. Am. Chem. Soc., 2002, 124: 489-493
[49] Deerenberg S, Schakel M, de Keijzer A H J F, Kraneburg M, Lutz M, Spek A L, Lammertsma K. Chem. Commun., 2002, 348-349
[50] Chan K L, McKiernan M J, Towns C R, Holmes A B. J. Am. Chem. Soc., 2005, 127: 7662-7663
[51] Chan K L, Watkins S E, Mak C S K., McKiernan M J, Towns C R, Pascu S I, Holmes A B. Chem. Commun., 2005, 5766-5768
[52] Zhang X, Jiang C, Mo Y, Xu Y, Shi H, Cao Y. Appl. Phys. Lett., 2006, 88: 629-633
[53] Chen R F, Fan Q L, Liu S J, Zhu R, Pu K Y, Huang W. Synth. Met., 2006, 156: 1161-1167
[54] Wang E G, Li C, Peng J B, Cao Y. J. Polym. Sci. Part A: Polym. Chem., 2007, 45 (21): 4941-4949
[55] Boudreault P L T, Alexandre M, Mario L. Macromol. Rapid Commun., 2007, 28(22): 2176-2179
[56] Lu G, Usta H, Risko C, Wang L, Facchetti A, Ratner M A, Marks T J. J. Am. Chem. Soc., 2008, 130(24): 7670-7685
[57] Li L C, Xu C H, Li S H. Tetrahedron Letters, 2010, 51(4): 622-624
[58] Ohshita J, Nodono M, Watanabe T, Ueno Y, Kunai A, Yamashita Y K, Ishikawa M. J. Organomet. Chem.,1998, 553: 487-491
[59] Usta H, Lu G, Facchetti A, Marks T J. J. Am. Chem. Soc., 2006, 128: 9034-9035
[60] Ohshita J, Hamamoto D, Kimura K, Kunai A. J. Organomet. Chem., 2005, 690: 3027-3032
[61] Chen W, Ijadi-Maghsoodi S, Barton T J. Polym. Prepr. Am. Chem. Soc., Div. Polym. Chem., 1997, 38: 189-190
[62] Zhang Z W, Li J, Huang B, Qin J G. Chemistry Letters, 2006, 35(8): 958-959
[63] Liao L, Cirpan A, Chu Q H, Karasz F E, Pang Y. J. Polym. Sci. Part A: Polym. Chem., 2007, 45(10): 2048-2058
[64] Ohshita J, Kimura K, Lee K H, Kunai A, Kwak Y W, Son E C, Kunugi Y. J. Polym. Sci. Part A: Polym. Chem., 2007, 45(20): 4588-4596
[65] Ohshita J J, Kai H, Kimura K, Lee K, Kunai A. Polymer Journal, 2009, 41(6): 482-485
[66] Kumar R, Wudl F. Abstracts of Papers, 239th ACS National Meeting, San Francisco, CA, United States, March 21-25, 2010
[67] He Y J, Zhao G J, Zhang M J, Min J, Li Y F. Synth. Met., 2010, 160(9/10): 1045-1049
[68] Zhang M J, Hai J, Guo X, He Y J, Zhang Z G, Min J, Zhang J, Zhao G J, Zhan X W, Li Y F. Macromolecules, 2010, 43(13): 5706-5712
[69] Ding J F, Song N H, Zhao L. Chem. Commun., 2010, 46:8668-8670
[70] Serby M, Ijadi-Maghsoodi S, Barton T J. 33rd Symposium on Organosilicon Chemistry, Saginaw, MI, 2000. PA-35
[71] Yamaguchi S, Xu C,Tamao K. J. Am. Chem. Soc., 2003, 125: 13662-13663
[72] Xu C H, Yamada H, Wakamiya A, Yamaguchi S, Tamao K. Macromolecules, 2004, 37(24): 8978-8983
[1] 杜瑾, 廖睿, 张幸林, 孙会彬, 黄维. 电致荧光变色材料的主要分类及变色机理[J]. 化学进展, 2018, 30(2/3): 286-294.
[2] 卢晓梅, 李杰, 胡文博, 邓卫星, 范曲立, 黄维. 水溶性共轭聚合物分子刷的研究进展[J]. 化学进展, 2016, 28(4): 528-540.
[3] 孙鹏飞, 候焕知, 范曲立, 黄维. 水溶性含糖共轭聚合物的制备及应用[J]. 化学进展, 2016, 28(10): 1489-1500.
[4] 马昀, 周妍, 杜文琦, 缪智辉, 祁争健. 基于共轭聚合物的核酸生物传感器的应用[J]. 化学进展, 2015, 27(12): 1799-1807.
[5] 王桂强, 段彦栋, 张娟, 林原, 禚淑萍. 染料敏化太阳能电池掺杂TiO2纳晶光阳极[J]. 化学进展, 2014, 26(07): 1255-1264.
[6] 孙花飞, 泮廷廷, 胡桂祺, 孙元伟, 王东亭, 张宪玺. 染料敏化太阳电池钌系敏化剂[J]. 化学进展, 2014, 26(04): 609-625.
[7] 任晓杰, 卢晓梅, 范曲立, 黄维. 共轭聚合物的双光子吸收性质及其在生物成像领域的应用[J]. 化学进展, 2013, 25(10): 1739-1750.
[8] 蔡小慧, 石琳, 刘兴奋*, 黄艳琴, 范曲立, 黄维*. 共轭聚合物的功能化及在生物/化学分析领域的应用[J]. 化学进展, 2013, 25(06): 975-989.
[9] 张力红, 于庆才, 万俊华*. 基于噻咯的聚合物给体光伏材料[J]. 化学进展, 2013, 25(05): 752-760.
[10] 张会京, 侯信* . 有机高分子/无机半导体杂化太阳能电池的发展现状与展望[J]. 化学进展, 2012, 24(11): 2106-2115.
[11] 朱春雷, 杨琼, 刘礼兵, 王树. 高灵敏共轭聚合物化学传感器[J]. 化学进展, 2011, 23(10): 1993-2002.
[12] 苗丽坤, 刘兴奋, 范曲立, 黄维. 基于荧光共轭聚合物的金属离子检测[J]. 化学进展, 2010, 22(12): 2338-2352.
[13] 刘勇 舒远杰 刘学涌 熊鹰 钟发春 孙毅. 分子印迹技术和荧光分析技术在爆炸物检测中的应用*[J]. 化学进展, 2009, 21(12): 2712-2717.
[14] 李迪 张龙 范曲立 黄维. 刚柔嵌段共轭聚合物自组装体系* [J]. 化学进展, 2009, 21(12): 2660-2673.
[15] 贺芳 王树. 基于水溶性共轭聚合物的蛋白质检测*[J]. 化学进展, 2009, 21(11): 2372-2378.
阅读次数
全文


摘要

含Silole共轭聚合物的光电性能