Sequence Analysis for Alternating Copolymers by MALDI-TOF-MS: Importance of Initiator Selectivity for Comonomer Pair

被引:15
作者
Nishimori, Kana [1 ]
Ouchi, Makoto [1 ,2 ]
Sawamoto, Mitsuo [1 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Polymer Chem, Nishikyo Ku, Kyoto 6158510, Japan
[2] Japan Sci & Technol Agcy JST, Precursory Res Embryon Sci & Technol PRESTO, 4-1-8 Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
alternating copolymerization; maleimides; radical polymerization; selectivity; sequences; N-SUBSTITUTED MALEIMIDES; MALEIC-ANHYDRIDE; POLYMERS; STYRENE; POLYMERIZATIONS; MECHANISM;
D O I
10.1002/marc.201600251
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A special initiator for metal-catalyzed living radical polymerization facilitates sequence analyses by matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS) of alternating copolymers from styrene and maleimide derivatives. The initiator is a malonate-based alkyl halide (DEMM-Br), in which two ester groups are attached on the carbon neighboring to bromide, and poor electron density of the radical species allows determination of next unit to the initiator in resultant alternating copolymers due to the selective initiation to styrene derivative. Thanks to the well-defined alpha-end group, sequence of the oligomeric products via radical copolymerization of PMS and EMI with DEMM-Br can be more simply analyzed by MALDI-TOF-MS, and indeed the following are clarified: the crossover propagation is almost perfectly controlled regardless of the injection ratio; a minor error event of the disordered alternating sequence containing St-St sequential unit could take place; the minor error can be suppressed with an excess amount of maleimide.
引用
收藏
页码:1414 / 1420
页数:7
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