Phase behavior and elastic properties of a slightly crosslinked liquid crystalline main-chain polymer

1990 ◽  
Vol 268 (3) ◽  
pp. 222-229 ◽  
Author(s):  
K. -H. Hanus ◽  
W. Pechhold ◽  
F. Soergel ◽  
B. Stoll ◽  
R. Zentel
1998 ◽  
Vol 24 (3) ◽  
pp. 375-379 ◽  
Author(s):  
J. LUB ◽  
D. J. BROER ◽  
M. E. MARTINEZ ANTONIO ◽  
G. N. MOL

2006 ◽  
Vol 514 (1-2) ◽  
pp. 165-173 ◽  
Author(s):  
Beate Sapich ◽  
Armelle B.E. Vix ◽  
Jürgen P. Rabe ◽  
Joachim Stumpe ◽  
Götz Wilbert ◽  
...  

2008 ◽  
Vol 41 (9) ◽  
pp. 3098-3108 ◽  
Author(s):  
Miguel Bispo ◽  
Daniel Guillon ◽  
Bertrand Donnio ◽  
Heino Finkelmann

e-Polymers ◽  
2001 ◽  
Vol 1 (1) ◽  
Author(s):  
Hendrik Wermter ◽  
Heino Finkelmann

AbstractNew nematic co-elastomers were synthesized which consist of a combination of nematic side- and main-chain polymers and where the liquid crystalline main-chain polymer can be considered as a macromolecular crosslinking component. By applying a mechanical field during the crosslinking process, the director of the nematic phase becomes macroscopically uniformly aligned and liquid-single-crystal elastomers were obtained. Within a narrow temperature regime, these networks can change their shape in one dimension by a factor > 3 and considerably improve the ability of being used as artificial muscles or mechanical actuators compared to the well known nematic side-chain elastomers. Networks having a non-ordered polydomain structure exhibit “soft (or semi-soft) elasticity” which is not only determined by a director reorientation process. Obviously, hairpin conformations within the main-chain segments contribute to this effect.


Soft Matter ◽  
2018 ◽  
Vol 14 (48) ◽  
pp. 9885-9900 ◽  
Author(s):  
Yongjian Wang ◽  
Kelly A. Burke

Tuning composition of main-chain liquid crystalline “Click” networks reveals long range order, even when hydrated, and shape morphing behaviors.


1995 ◽  
Vol 33 (6) ◽  
pp. 891-897 ◽  
Author(s):  
A. Uedono ◽  
R. Sadamoto ◽  
T. Kawano ◽  
S. Tanigawa ◽  
T. Uryu

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