OALib Journal期刊
ISSN: 2333-9721
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溶剂手性转移法制备超支化共轭聚合物手性荧光纳米粒子
DOI: 10.3724/SP.J.1105.2013.12404, PP. 426-435
Keywords: 手性转移,柠檬烯,超支化聚合物,荧光纳米粒子,手性纳米粒子,自组装
Abstract:
通过Suzuki缩合反应制备了一系列新型不同超支化结构的9,9-二辛基芴-联二噻吩交替共聚物(HF8T2s).以手性溶剂(R)-(+)-/(S)-(-)-柠檬烯为手性源,在三氯甲烷/((R)-(+)-或(S)-(-)-)柠檬烯/甲醇混合溶剂体系里,通过溶剂手性转移技术,制备了分别以三苯胺、三苯基苯和螺二芴为支化单元的超支化聚(9,9-二辛基芴-联二噻吩)手性荧光纳米粒子.在混合溶剂中形成的荧光纳米粒子的手性来源于手性溶剂(R)-(+)-/(S)-(-)-柠檬烯.以三苯胺为支化单元时,支化单元的含量为4.56%时聚合物的手性信号最强,支化单元的含量为6.76%时聚合物的手性信号消失.以三苯基苯和螺二芴为支化单元时,支化单元的含量分别为1.85%(三苯基苯)和1.78%(螺二芴)时聚合物的手性信号最强,支化单元的含量较高(三苯基苯4.68%和6.56%,螺二芴4.54%和6.54%)时聚合物的手性信号消失.以超支化聚合物HF8T2-TRA2(三苯胺为支化单元,支化单元含量为1.90%)为例,考察了超支化聚合物重复单元浓度、弱溶剂的种类、弱溶剂与手性溶剂比例和(R)-(+)-柠檬烯与(S)-(-)-柠檬烯比例对超支化聚合物圆二色谱光谱强度的影响.当超支化聚合物重复单元浓度为5.0×10-5mol/L,使用甲醇为弱溶剂,三氯甲烷/((R)-(+)-或(S)-(-)-)柠檬烯/甲醇之间的配比为0.3∶1.8∶0.9(V/V/V)时,超支化聚合物圆二色谱光谱强度最强.在三氯甲烷/((R)-(+)-或(S)-(-)-)柠檬烯/甲醇(0.3∶1.8∶0.9(V/V/V))混合溶剂中,聚合物重复单元浓度为5.0×10-5mol/L,超支化聚合物在350~550nm有较强的紫外吸收,在450~700nm有较强的荧光发射,组装成的荧光纳米粒子尺寸约为500~2000nm.
References
[1] | 1 Qing G Y,Sun T L.NPG Asia Mater,2012,4(1):e4
|
[2] | 2 Zhang M X,Qing G Y,Sun T L.Chem Soc Rev,2012,41(5):1927~1984
|
[3] | 3 Shan Xingxing(单星星),Chen Wenrui(陈文锐),Qing Guangyan(卿光焱),Sun Taolei(孙涛垒),Lei Jiaheng(雷家珩).Acta Polymerica Sinica(高分子学报),2012,(10):1082~1090
|
[4] | 5 Li Zifa(李自法),Zheng Shijun(郑世军),Zhang Shuyuan(张淑媛),Zhou Qingjie(绉清洁),Zhou Qifeng(周其凤),Zhang Dong(张东).Acta Polymerica Sinica(高分子学报),2000,(1):14~18
|
[5] | 6 Cao Hongqing(曹洪庆),Cui Jiaxi(崔家喜),Liu Anhua(刘安华),Wan Xinhua(宛新华).Acta Polymerica Sinica(高分子学报),2010,(2):222~230
|
[6] | 7 Nakano T,Okamoto Y.Chem Rev,2001,101:4013-4038
|
[7] | 13 Nakashima H,Koe J R,Torimitsu K,Fujiki M.J Am Chem Soc,2001,123:4847~4848
|
[8] | 15 Buono A M,Immediata I,Rizzo P,Guerra G.J Am Chem Soc,2007,129:10992~10993
|
[9] | 16 Nakano Y,Liu Y,Fujiki M.Polym Chem,2010,1:460~469
|
[10] | 24 Liu Jinjun(刘进军),Qin Hong(秦红).Journal of Molecular Science(分子科学学报),2010,26(6):389~395
|
[11] | 25 Yu J M,Sakamoto T,Watanabe K,Furumi S,Tamaoki N,Chenb Y,Nakano T.Chem Commun,2011,47:3799~3801
|
[12] | 26 Wang R,Wang W Z,Yang G Z,Liu T X,Yu J S,Jiang Y D.J Polym Sci:Part A:Polym Chem,2008,46:790~802
|
[13] | 27 Nakako H,Nomura R,Masuda T.Macromolecules,2001,34:1496~1502
|
[14] | 4 Cui Jiaxi(崔家喜),Wan Xinhua(宛新华).Acta Polymerica Sinica(高分子学报),2011,(10):1202~1207
|
[15] | 8 Li Ping(李萍),Hu JunZhe(胡濬喆),Lin Baoping(林保平),Rong Fei(戎非),Yuan Chunwei(袁春伟).Acta Chimica Sinica(化学学报),2003,61(11):1885~1889
|
[16] | 9 Rai R,Saxena A,Ohira A,Fujiki M.Langmuir,2005,21:3957~3962
|
[17] | 10 Nakano Y,Liu Y,Fujiki M.Polym Chem,2010,(1):460~469
|
[18] | 11 Pan Xiujuan(潘秀娟),Jiang Hao(蒋皓),Wang Yali(王亚丽),Zhou Gang(邹纲),Zhang Qijin(张其锦).Progress In Chemistry(化学进展),2010,22(10):2014~2023
|
[19] | 12 Green M M,Khatri C,Peterson N C.J Am Chem Soc,1993,115:4941~4942
|
[20] | 14 Nakano Y,Fujiki M.Macromolecules,2011,44:7511~7519
|
[21] | 17 Zhang W,Yoshida K,Fujiki M,Zhu X L.Macromolecules,2011,44:5105~5111
|
[22] | 18 Bernius M,Inbasekaran M,Woo E,Wu W S,Wujkowski L.J Mater Sci:Mater Electronics,2000,11:111~116
|
[23] | 19 Hou Qiong(侯琼),Niu Yuhua(牛于华),Yang Wei(杨伟),Yang Renqiang(阳仁强),Yuan Min(袁敏),Cao Yong(曹镛).Acta Polymerica Sinica(高分子学报),2003,(2):161~165
|
[24] | 20 Tang Chao(唐超),Liu Feng(刘烽),Xu Hui(徐慧),Huang Wei(黄维).Progress in Chemistry(化学进展),2007,19(10):1553~1561
|
[25] | 21 Voit B.J Polym Sci Part A:Polym Chem,2005,43:2679~2699
|
[26] | 22 He Qingguo(贺庆国),Lin Tong(林童),Bai Fenglian(白凤莲).Chinese Science Bulletin(科学通报),2011,45(22):2376~2383
|
[27] | 23 Sun Wenbin(孙文彬),Chen Zhao(陈钊),Zhang Bin(张斌),Yang Wei(杨伟),Cao Yong(曹镛).New Chemical Materials(化工新型材料),2007,35(8):28~33
|
[28] | 28 Liu J H,Yan J J,Chen E Q,Jacky W.Y,Dong Y P,Liang D H,Tang B Z.Polymer,2008,49:3366~3370
|
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