K. Takenaka, Mayumi Arimoto, Hiroki Takeshita, M. Miya, T. Shiomi
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引用次数: 0
摘要
在不同的条件下,自由基聚合了含有两个膦酸二乙酯功能的1,3-丁二烯衍生物四乙基(2,3-二亚甲基丁烷-1,4-二基)二膦酸盐。在苯中,以1 mol%的2,2′-偶氮二异丁腈为引发剂,在60℃下聚合21 h,得到了产率为70%的粘性聚合物,未形成凝胶。基于聚苯乙烯校准,以N, N -二甲基甲酰胺作为洗脱剂,由此获得的聚合物的数平均分子量通过SEC估计为69,000。聚合速率分别与引发剂的0.5和1.5次方成正比,与单体浓度成正比。聚合反应的总活化能为91.4 kJ/mol。聚合物的微观结构完全为1,4-,但同时包含E和Z两种构型。该聚合物的玻璃化转变温度为- 18℃,单体与苯乙烯为共聚物的反应性比为r st =0.15;
Free-radical polymerization of tetraethyl (2,3-dimethylenebutane-1,4-diyl)bis(phosphonate)
Free-radical polymerization of tetraethyl (2,3-dimethylenebutane-1,4-diyl)bis(phosphonate), a 1,3-butadi-ene derivative containing two diethyl phosphonate functions in a molecule, was carried out under various conditions. When polymerization was performed in benzene at 60 ° C for 21 h with using 1 mol% of 2,2 ′ -azobisisobutyronitrile as an initiator, sticky polymer was obtained in 70% yield without forming gel. Number average molecular weight of the polymer thus obtained was estimated to be 69,000 by SEC based on polystyrene calibration using N , N -dimethylformamide as an eluent. The rate of polymerization was found to be proportional to 0.5 and 1.5 power of the initiator and the monomer concentration, respectively. The overall activation energy of polymerization was determined to be 91.4 kJ/mol. The microstructure of the polymer was exclusively 1,4- but both E and Z configurations were contained. Glass transition temperature of the polymer was − 18 ° C. Monomer reactivity ratio of the monomer with styrene as comonomer was determined to be r st =0.15,