Diblock copolymer of bacterial cellulose and poly(methyl methacrylate) initiated by chain-end-type radicals produced by mechanical scission of glycosidic linkages of bacterial cellulose.
Diblock copolymer of bacterial cellulose and poly(methyl methacrylate) initiated by chain-end-type radicals produced by mechanical scission of glycosidic linkages of bacterial cellulose.
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DOI:
10.1021/bm100879v
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发表时间:
2010-09
影响因子:
6.2
通讯作者:
M. Sakaguchi;T. Ohura;T. Iwata;Shuhei Takahashi;S. Akai;Toshiyuki Kan;H. Murai;M. Fujiwara;O. Watanabe;Mamiko Narita
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文献类型:
--
作者:
M. Sakaguchi;T. Ohura;T. Iwata;Shuhei Takahashi;S. Akai;Toshiyuki Kan;H. Murai;M. Fujiwara;O. Watanabe;Mamiko Narita
Bacterial cellulose (BC) was mechanically fractured in vacuum at 77 K; this resulted in the scission of the β-1,4 glycosidic linkages of BC. The chain-end-type radicals (mechanoradicals) generated from the scissions were assigned by electron spin resonance (ESR) spectral analyses. A diblock copolymer of BC and poly(methyl methacrylate) (BC-block-PMMA) was produced by the mechanical fracture of BC with MMA (methyl methacrylate) in vacuum at 77 K. Radical polymerization of MMA was initiated by the mechanoradicals located on the BC surface. The BC surface was fully covered with the PMMA chains of the BC-block-PMMA. Novel modification of the BC surface with the BC-block-PMMA was confirmed by spectral analyses of ESR, Fourier-transform infrared, (1)H NMR, and gel permeation chromatography.