Cyclopolymerization of 2-ethynyl-N-propargylpyridinium tetraphenylborate by transition metal catalysts

被引:0
|
作者
Gal, YS [1 ]
Jin, SH
Gui, TL
Lee, WC
Yun, NG
Park, SH
Lee, SS
Bae, JS
机构
[1] Kyungil Univ, Coll Gen Educ, Polymer Chem Lab, Kyungbuk 712701, South Korea
[2] Pusan Natl Univ, Dept Chem Educ, Pusan 609735, South Korea
[3] Harbin Univ Sci & Technol, Dept Mat Phys, Harbin 150080, Peoples R China
[4] Kyungil Univ, Dept Text & Fas Technol, Kyungbuk 712701, South Korea
[5] Agcy Def Dev, Composite Mat Lab, Taejon 305600, South Korea
[6] Hanbat Natl Univ, Dept Chem Engn, Taejon 305719, South Korea
[7] Dankook Univ, Dept Chem Technol, Chungnam 330714, South Korea
关键词
cyclopolymerization; 2-ethynylpyridine; transition metal catalyst; morphology;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new conjugated ionic cyclopolymer having a bulky tetraphenylborate counter ion, poly (2-ethynyl-N-propargylpyridinium tetraphenylborate), was synthesized via ring-forming polymerization of the corresponding diacetylenic monomer. The polymerization of 2-ethynyl-N-propargylpyridinium tetraphenylborate was performed using various transition metal catalysts. In general, the polymerization of this diacetylenic monomer proceeded well to give a high yield of polymer. The catalytic activities of a W-based catalyst were similar with those of Mo-based catalysts. The resulting polymers were mostly brown or black powders. The polymer structure was characterized through elemental analysis and NMR, IR, and UV-visible spectroscopies to confirm the conjugated cyclopolymer structure and its tetraphenylborate counter ions. The inherent viscosities of the resulting polymers were in the range 0.09 similar to 0.16 dL/g, depending on the polymerization conditions. The thermal and morphological properties of the polymers were also studied and are discussed.
引用
收藏
页码:432 / 438
页数:7
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