Synthesis and chiral recognition ability of optically active poly{N-[(R)-?-methoxycarbonylbenzyl]methacrylamide} with various tacticities by radical polymerization using Lewis acids

2003 ◽  
Vol 41 (21) ◽  
pp. 3354-3360 ◽  
Author(s):  
Kohei Morioka ◽  
Yoshikatsu Suito ◽  
Yutaka Isobe ◽  
Shigeki Habaue ◽  
Yoshio Okamoto
2016 ◽  
Vol 45 (9) ◽  
pp. 1063-1065 ◽  
Author(s):  
Katsuhiro Maeda ◽  
Miyuki Maruta ◽  
Kouhei Shimomura ◽  
Tomoyuki Ikai ◽  
Shigeyoshi Kanoh

1987 ◽  
Vol 60 (9) ◽  
pp. 3341-3345 ◽  
Author(s):  
Yun Chen ◽  
Kazuhiko Saigo ◽  
Noriyuki Yonezawa ◽  
Kouzou Tachibana ◽  
Masaki Hasegawa

2013 ◽  
Vol 49 (11) ◽  
pp. 3673-3680 ◽  
Author(s):  
Xiaodong Xu ◽  
Siwei Feng ◽  
Yuanqi Zhu ◽  
Han Li ◽  
Xiande Shen ◽  
...  

Polymer ◽  
2009 ◽  
Vol 50 (2) ◽  
pp. 404-409 ◽  
Author(s):  
Xiujuan Xi ◽  
Guangxuan Liu ◽  
Wei Lu ◽  
Liming Jiang ◽  
Weilin Sun ◽  
...  

2014 ◽  
Vol 887-888 ◽  
pp. 688-692
Author(s):  
Zheng Fu ◽  
Hong Wei ◽  
Chao Yuan ◽  
Zhong Wen Li

The radical polymerization of optically active methacrylamide derivatives, N-[o-(4-phenyl-4,5-dihydro-1,3-oxazol-2-yl) phenymethacrylamide ((R)-PhOPMAM) and N-[o-(4-isopropyl-4,5-dihydro-1,3-oxazol-2-yl) phenymethacrylamide ((S)-PriOPMAM), were carried out under various conditions. The effect of the Lewis acid, that is, rare earth metal trifluoromethanesulfonates on the free-radical polymerization were examined under different solvents. The Lewis acids are effective in enhancing the isotacticity in the polymerization of (S)-PriOPMAM. The same phenomenon were not happened in the polymerization of (R)-PhOPMAM. The polymerization characteristics and the chiroptical behavior of the resultant polymers have been examined by using circular dichroism (CD), UVVis, and NMR spectroscopies.


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