一类供体-受体双嵌段丙烯酸酯聚合物的合成及性能

孙志敏;周曼溪;朱磊;李齐方*;陈广新

北京化工大学学报(自然科学版) ›› 2012, Vol. 39 ›› Issue (3) : 50-54.

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北京化工大学学报(自然科学版) ›› 2012, Vol. 39 ›› Issue (3) : 50-54.
材料科学与工程

一类供体-受体双嵌段丙烯酸酯聚合物的合成及性能

  • 孙志敏;周曼溪;朱磊;李齐方*;陈广新
作者信息 +

Synthesis and study of the properties of a donor-acceptor diblock acrylate copolymer

  • SUN ZhiMin;ZHOU ManXi;ZHU Lei;LI QiFang;CHEN GuangXin
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文章历史 +

摘要

利用原子转移自由基聚合(ATRP)法合成了一种新的供体-受体双嵌段聚合物聚对(二苯胺基)苯乙烯-聚(2-(2-蒽醌甲酰氧基)甲基丙烯酸乙酯(P1-b-P2)。供体段是富电子的三苯胺段,受体段是缺电子的蒽醌段。该双嵌段聚合物的单体结构通过核磁(NMR)加以表征,聚合物通过凝胶渗透色谱(GPC)、差示扫描量热法(DSC)、紫外光谱(UV-vis)、荧光光谱(PL)和循环伏安(CV)法加以表征。GPC和紫外吸收测试表明聚合物数均分子量约为7600,最大吸收波长为305nm,CV测试计算发现受体段比供体段长,与GPC测试结果一致,表现出更好的受体性能。

Abstract

A new diblock copolymer P1-b-P2 containing substituted triphenylamine as hole transport moieties and substituted 9,10-anthraquinone as electron transport moieties has been synthesized by atom transfer radical polymerization (ATRP). The structures of the monomers and the polymer were characterized by nuclear magnetic resonance (NMR) spectroscopy, gel permeation chromatography (GPC) and differential scanning calorimetry (DSC). The diblock copolymer exhibited a relatively narrow molecular weight distribution with a number-average molecular weight ( Mn) of 7600. The photoelectric properties of the diblock copolymer were investigated by UV-vis and fluorescence spectroscopy, and cyclic voltammetry (CV). The UV-vis spectrum showed a λmax value of 305nm, whilst the CV showed that the donor segment is short, while the acceptor segment is long. Therefore the polymer exhibits predominantly acceptor properties. This is consistent with the GPC results.

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孙志敏;周曼溪;朱磊;李齐方*;陈广新. 一类供体-受体双嵌段丙烯酸酯聚合物的合成及性能[J]. 北京化工大学学报(自然科学版), 2012, 39(3): 50-54
SUN ZhiMin;ZHOU ManXi;ZHU Lei;LI QiFang;CHEN GuangXin. Synthesis and study of the properties of a donor-acceptor diblock acrylate copolymer [J]. Journal of Beijing University of Chemical Technology, 2012, 39(3): 50-54

参考文献

[1]Li Y W, Xue L L, Li H, et al. Energy level and molecular structure engineering of conjugated donor-acceptor copolymers for photovoltaic applications[J]. Macromolecules, 2009, 42(13): 4491-4499.
[2]Clarke T M, Durrant J R. Charge photogeneration in organic solar cells[J]. Chem Rev, 2010, 110(11): 6736-6767.
[3]Park J K, Jo J, Seo J H, et al. End-capping effect of a narrow bandgap conjugated polymer on bulk heterojunction solar cells[J]. Adv Mater, 2011, 23(21): 2430-2435.
[4]Kim J Y, Lee K, Coates N E, et al. Efficient tandem polymer solar cells fabricated by all-solution processing[J]. Science, 2007, 317: 222-225.
[5]Liang Y Y, Xu Z, Xia J B, et al. For the bright future-bulk heterojunction polymer solar cells with power conversion efficiency of 7.4%[J]. Adv Mater, 2010, 22(20): E135-E138.
[6]Yang X N, Loos J, Veenstra S C, et al. Nanoscale morphology of highperformance polymer solar cells[J]. Nano Lett, 2005, 5(4): 579-583.
[7]Erb T, Zhokhavets U, Gobsch G, et al. Correlation between structural and optical properties of composite polymer/fullerene films for organic solar cell[J]. Adv Funct Mater, 2005, 15(7): 1193-1196.
[8]Lee H J, Sohn J, Hwang J, et al. Triphenylamine-cored bifunctional organic molecules for twophoton absorption 〖JP3〗and photorefraction[J]. Chem Mater, 2004, 16(3): 456-465.
[9]Zagotto G, Sissi C, Moro S, et al. Amide bond direction modulates G-quadruplex recognition and telomerase inhibition by 2,6 and 2,7 bis-substituted anthracenedione derivatives[J]. Bioorganic & Medicinal Chemistry, 2008, 16(1): 354-361.
[10]Tong Y Y, Dong Y Q, Du F S, et al. Synthesis of welldefined poly(vinyl acetate)-b-polystyrene by combination of ATRP and RAFT polymerization[J]. Macromolecules, 2008, 41(20): 7339-7346.
[11]李茂, 路萍, 张海全, 等. 含芴聚合物电子亲合能和电离能的确定[J]. 发光学报, 2006, 27(1): 80-83.
Li M, Lu P, Zhang H Q, et al. Electrochemical determination of the ionization potential and electron affinity of PF derivatives[J]. Chinese J Lumin, 2006, 27(1): 80-83. (in Chinese)
[12]Segura J L, Gómez R, Blanco R, et al. Synthesis and electronic properties of anthraquinone-, tetracyanoanthraquinodimethane-, and perylenetetracarboxylic diimide-functionalized poly(3,4-ethylenedioxythiophenes) [J]. Chem Mater, 2006, 18(12): 2834-2847.
[13]Zhang Y, Yip H L, Acton O, et al. A simple and effective way of achieving highly efficient and thermally stable bulk-heterojunction polymer solar cells using amorphous fullerene derivatives as electron acceptor[J]. Chem Mater, 2009, 21(13): 2598-2600.
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