Synthesis of Heterotelechelic α,ω-Dye-Labeled Polymer and Energy Transfer between the Chain Ends

被引:14
|
作者
Sha, Ye [1 ]
Xu, Yunlong [2 ]
Qi, Dongliang [1 ]
Wan, Yuanxin [1 ]
Li, Linling [1 ]
Li, Hong [2 ]
Wang, Xiaoliang [1 ]
Xue, Gi [1 ]
Zhou, Dongshan [1 ,3 ,4 ]
机构
[1] Nanjing Univ, Key Lab High Performance Polymer Mat & Technol, Sch Chem & Chem Engn,Minist Educ,Dept Polymer Sci, State Key Lab Coordinat Chem,Nanjing Natl Lab Mic, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Environm, State Key Lab Pollut Control & Resource Reuse, Nanjing 210046, Jiangsu, Peoples R China
[3] Yili Normal Univ, Sch Phys Sci & Technol, Xinjiang Key Lab, Yining 835000, Peoples R China
[4] Yili Normal Univ, Phase Transit & Microstruct Condensed Matters, Yining 835000, Peoples R China
关键词
TRANSFER RADICAL POLYMERIZATION; CLICK CHEMISTRY; RAFT POLYMERIZATION; LIVING CELLS; PH; SENSOR; FUNCTIONALITY; DIFFUSION; DYNAMICS; GROWTH;
D O I
10.1021/acs.macromol.6b01726
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report on the synthesis of heterotelechelic alpha,omega-dyelabeled polystyrene and poly(methyl methacrylate) via a combination of site-specific atom transfer radical polymerization (ATRP) and click chemistry. By using the advantages of the living polymerization characteristics and a robust coupling efficiency, the Forster/fluorescence resonance energy transfer (FRET) pairs (i.e., carbazolyl and anthryl) were dictated to be at the near-stoichiometric chain ends. The distribution of the end-to-end distance was well described by the energy transfer response of the fluorescent groups between chain ends, which is in reasonable agreement with Gaussian statistics. The synthetic approach described here provides an opportunity to prepare polymeric materials with customized responsive elements and in-depth insight into the statistical scaling dimension of polymers.
引用
收藏
页码:8274 / 8281
页数:8
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