A novel type of optically active helical polymers:: Synthesis and characterization of poly(N-propargylureas)

被引:62
作者
Deng, Jianping [1 ]
Luo, Xiaofeng [2 ]
Zhao, Weiguo [2 ]
Yang, Wantai [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Coll Mat Sci & Engn, Beijing 100029, Peoples R China
关键词
chiral; circular dichroism; conjugated polymers; helical structure; polyacetylenes;
D O I
10.1002/pola.22755
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This article presents two novel artificial helical polymers, substituted polyacetylenes with urea groups in side chains. Poly(4) and poly(5) can be obtained in high yields (>= 97%) and with moderate molecular weights (11,000-14,000). Poly(4) contains chiral centers in side chains, and poly(5) is an achiral polymer. Both of the two polymers adopted helical structures under certain conditions. More interestingly, poly(4) exhibited large specific optical rotations, resulting from the predominant one-handed screw sense. The helical conformation in poly(5) was stable against heat, while poly(4) underwent conformational transition from helix to random coil upon increasing temperature from 0 to 55 degrees C. Solvents had considerable influence on the stability of the helical conformation in poly(4). The screw sense adopted by the helices was also largely affected by the nature of the solvent. Poly(4-co-5)s formed helical conformation and showed large optical rotations, following the Sergeants and Soldiers rule. By comparing the present two polymers (with one -N-H groups) with the three polymers previously reported (with two -N-H groups in side chains), the nature of the hydrogen bonds formed between the neighboring urea groups played big roles in the formation of stable helical conformation. (c) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:4112 / 4121
页数:10
相关论文
共 55 条
[1]   Morphological control and molecular recognition by bis-urea hydrogen bonding in micelles of amphiphilic tri-block copolymers [J].
Chebotareva, N ;
Bomans, PHH ;
Frederik, PM ;
Sommerdijk, NAJM ;
Sijbesma, RP .
CHEMICAL COMMUNICATIONS, 2005, (39) :4967-4969
[2]   Organocatalysis mediated by (thio)urea derivatives [J].
Connon, Stephen J. .
CHEMISTRY-A EUROPEAN JOURNAL, 2006, 12 (21) :5418-5427
[3]   Steric control over hydrogen bonding in crystalline organic solids:: A structural study of N,N′-dialkylthioureas [J].
Custelcean, R ;
Gorbunova, MG ;
Bonnesen, PV .
CHEMISTRY-A EUROPEAN JOURNAL, 2005, 11 (05) :1459-1466
[4]  
De Clercq E, 2002, MED RES REV, V22, P531
[5]  
de Loos M, 2001, ANGEW CHEM INT EDIT, V40, P613, DOI 10.1002/1521-3773(20010202)40:3<613::AID-ANIE613>3.0.CO
[6]  
2-K
[7]   Synthesis of novel mono-substituted polyacetylenes bearing functional urea groups in side chains [J].
Deng, Hanping ;
Zhao, Weiguo ;
Yang, Wantai .
REACTIVE & FUNCTIONAL POLYMERS, 2007, 67 (09) :828-835
[8]   Synthesis and characterization of N-propargyl cinnamamide polymers and copolymers [J].
Deng, Jianping ;
Wang, Jianmin ;
Zhao, Weiguo ;
Zhang, Zhigang ;
Yang, Wantai .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2007, 208 (03) :316-323
[9]   The formation of a stable, helical conformation in poly(N-propargylamides) through synergic effects among their pendent groups [J].
Deng, Jianping ;
Zhao, Weiguo ;
Wang, Jianmin ;
Zhang, Zhigang ;
Yang, Wantai .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2007, 208 (02) :218-223
[10]   Variation of helical pitches driven by the composition of N-propargylamide copolymers [J].
Deng, JP ;
Tabei, J ;
Shiotsuki, M ;
Sanda, F ;
Masuda, T .
MACROMOLECULES, 2004, 37 (26) :9715-9721