Synthesis of telechelic C 60 end‐capped polymers under microwave irradiation
Abstract Bromo‐Double‐Terminated polystyrene (Br‐PSt‐Br) and poly(methyl methacrylate) (Br‐PMMA‐Br) with predesigned molecular weight and narrow polydispersity were prepared by atom transfer radical polymerization (ATRP) using the initiating system aa′‐dibromo‐ p ‐xylene(DBX) / CuBr/2,2′‐bipyridine(...
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Published in | Journal of applied polymer science Vol. 99; no. 3; pp. 828 - 834 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
05.02.2006
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Online Access | Get full text |
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Abstract | Abstract
Bromo‐Double‐Terminated polystyrene (Br‐PSt‐Br) and poly(methyl methacrylate) (Br‐PMMA‐Br) with predesigned molecular weight and narrow polydispersity were prepared by atom transfer radical polymerization (ATRP) using the initiating system aa′‐dibromo‐
p
‐xylene(DBX) / CuBr/2,2′‐bipyridine(bipy). The precursor bromo‐terminated polymers were subsequently functionalized with fullerene C
60
using CuBr/bipy as the catalyst system under microwave irradiation (MI). The telechelic C
60
end‐capped products were characterized by gel permeation chromatography (GPC), UV‐vis, FT‐IR, TGA, DSC,
1
H NMR, and
13
C NMR. The results showed that microwave irradiation could significantly increase the rate of fullerenation reaction, and the physical properties and structure of the C
60
end‐capped polymers are not modified by the use of the microwave. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 828–834, 2006 |
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AbstractList | Abstract
Bromo‐Double‐Terminated polystyrene (Br‐PSt‐Br) and poly(methyl methacrylate) (Br‐PMMA‐Br) with predesigned molecular weight and narrow polydispersity were prepared by atom transfer radical polymerization (ATRP) using the initiating system aa′‐dibromo‐
p
‐xylene(DBX) / CuBr/2,2′‐bipyridine(bipy). The precursor bromo‐terminated polymers were subsequently functionalized with fullerene C
60
using CuBr/bipy as the catalyst system under microwave irradiation (MI). The telechelic C
60
end‐capped products were characterized by gel permeation chromatography (GPC), UV‐vis, FT‐IR, TGA, DSC,
1
H NMR, and
13
C NMR. The results showed that microwave irradiation could significantly increase the rate of fullerenation reaction, and the physical properties and structure of the C
60
end‐capped polymers are not modified by the use of the microwave. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 828–834, 2006 |
Author | Wu, Huixia Chen, Wei Cai, Ruifang Li, Feng Yang, Ming Lin, Yanghui |
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CitedBy_id | crossref_primary_10_1002_marc_201000539 crossref_primary_10_1071_CH07219 crossref_primary_10_1021_ma102754c crossref_primary_10_1002_marc_200600749 crossref_primary_10_1002_pen_20491 crossref_primary_10_1039_c3ra41812j crossref_primary_10_1016_j_carbon_2006_07_011 crossref_primary_10_1021_jp9114578 crossref_primary_10_1002_app_30833 crossref_primary_10_1080_10601325_2011_614847 |
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Bromo‐Double‐Terminated polystyrene (Br‐PSt‐Br) and poly(methyl methacrylate) (Br‐PMMA‐Br) with predesigned molecular weight and narrow polydispersity... |
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Title | Synthesis of telechelic C 60 end‐capped polymers under microwave irradiation |
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