scholarly journals Stereochemistry in Anionic Polymerization of Styrene Derivatives Bearing Optically Active Amino Groups at ortho-Position

2002 ◽  
Vol 34 (2) ◽  
pp. 57-62 ◽  
Author(s):  
Hiroharu Ajiro ◽  
Shigeki Habaue ◽  
Yoshio Okamoto
2004 ◽  
Vol 36 (4) ◽  
pp. 323-328 ◽  
Author(s):  
Hiroharu Ajiro ◽  
Shigeki Habaue ◽  
Yoshio Okamoto

Polymer ◽  
2010 ◽  
Vol 51 (24) ◽  
pp. 5712-5718 ◽  
Author(s):  
Yunkai Sun ◽  
Nianfa Yang ◽  
Ji Liu ◽  
Jing Cao ◽  
Hang Gong

Polymer ◽  
2004 ◽  
Vol 45 (3) ◽  
pp. 849-854 ◽  
Author(s):  
Fumio Sanda ◽  
Yosuke Yukawa ◽  
Toshio Masuda

2005 ◽  
Vol 41 (11) ◽  
pp. 2592-2601 ◽  
Author(s):  
Xiujuan Xi ◽  
Liming Jiang ◽  
Weilin Sun ◽  
Zhiquan Shen

1995 ◽  
Vol 16 (11) ◽  
pp. 845-849
Author(s):  
Howard Haubenstock ◽  
Wei-Hong Yu ◽  
George Odian

2008 ◽  
Vol 41 (12) ◽  
pp. 4235-4244 ◽  
Author(s):  
Kenji Sugiyama ◽  
Kenji Watanabe ◽  
Akira Hirao ◽  
Mayumi Hayashi

2014 ◽  
Vol 92 (7) ◽  
pp. 647-652
Author(s):  
Yehui Chen ◽  
Liwen Yang ◽  
Nianfa Yang ◽  
Zhusheng Yang

(S)-3-acrylyl-2,2′-bis(methoxymethoxy)-1,1′-binaphthyl (3a) was synthesized and anionically polymerized using n-BuLi as an initiator. The polymer derived from 3a had a tremendous specific optical rotation [Formula: see text] = −304.2, while that of the monomer 3a is −68.7. Poly-3a was confirmed to exist in the form of a one-handed helical structure in solution by means of comparing the specific optical rotation, the circular dichroism, and UV-vis spectra with that of 3a and the model compounds such as (S)-3-propionyl-2,2′-bis(methoxymethoxy)-1,1′-binaphthyl (3b) and (S)-3-heptanoyl-2,2′-bis(methoxymethoxy)-1,1′-binaphthyl (3c). This conclusion was also confirmed by the fact that the g value of poly-3a is about 15 times of that of the monomer 3a.


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