Liquid Crystal Elastomers with Piezoelectric Properties

MRS Bulletin ◽  
1991 ◽  
Vol 16 (1) ◽  
pp. 29-31 ◽  
Author(s):  
Wolfgang Meier ◽  
Heino Finkelmann

During the last few years, liquid crystalline elastomers (LCEs) have been systematically produced by cross-linking liquid crystalline side-chain polymers. In these networks, a liquid crystalline molecule is fixed at each monomeric unit. LCEs exhibit a novel combination of properties. Due to liquid crystalline groups, they show anisotropic liquid crystalline properties similar to conventional liquid crystals (LCs); but due to the three-dimensional network-structure of the polymer chains, they show typical elastomer properties, such as rubber elasticity or shape stability. One exceptional property of this combination is demonstrated when a mechanical deformation to the LCE causes macroscopically uniform orientation of the long molecular axis of the LC units (the so-called “director”).This response of the LC-phase structure to an applied mechanical field is similar to the effect of electric or magnetic fields on low molecular weight liquid crystals (LMLC), as illustrated in Figure 1. Figure la shows an undeformed LCE. Because of the non-uniform orientation of the director, the sample scatters light strongly so the elastomer is translucent like frosted glass. On the other hand, applying a mechanical field the director becomes uniformly aligned and the sample is transparent (Figure 1b). Such a macroscopically ordered rubber exhibits optical properties very similar to single crystals. These propertie s of LCEs offer new prospects for technical application, e.g., in nonlinear and integrated optics.

1986 ◽  
Vol 59 (4) ◽  
pp. 541-550 ◽  
Author(s):  
Kyung-Do Suh ◽  
Hidetoshi Oikawa ◽  
Kenkichi Murakami

Abstract From the experimental results of the present investigation, it is apparent that two kinds of networks which have a different three-dimensional network structure give quite different behavior of chemical stress relaxation, even if both networks have the same network chain density. The difference in three-dimensional network structure for the two kinds of rubber arises from the degree of entanglement, which changes with the concentration of the polymer chains prior to the crosslinking process. The direct cause of chemical relaxation is due to the scission of network chains by degradation, whereas the total relaxation is caused by the change of geometrical conformation of network chains. This then casts doubt on the basic concept of chemorheology which is represented by Equation 2.


2015 ◽  
Vol 71 (3) ◽  
pp. o195-o196
Author(s):  
J. Govindaraj ◽  
R. Raja ◽  
M. Suresh ◽  
R. Raghunathan ◽  
A. SubbiahPandi

In the title compound, C35H27N3O3S, the spiro-linked five-membered rings both adopt twisted conformations. The pyrrolidine ring makes dihedral angles of 80.5 (1) and 77.4 (9)° with the benzothiophene ring system and the quinoxaline ring system, respectively. The S atom and C=O unit of the benzothiophene ring system are disordered over two opposite orientations in a 0.768 (4):0.232 (4) ratio. The atoms of the ethyl side chain are disordered over two sets of sites in a 0.680 (16):0.320 (16) ratio. In the crystal, molecules are linked by C—H...O, C—H...N and π–π interactions [shortest centroid–centroid distance = 3.4145 (19) Å], resulting in a three-dimensional network.


2015 ◽  
Vol 71 (10) ◽  
pp. 929-935 ◽  
Author(s):  
Hyun-Chul Kim ◽  
Ja-Min Gu ◽  
Seong Huh ◽  
Chul-Hyun Yo ◽  
Youngmee Kim

Two new one-dimensional CuIIcoordination polymers (CPs) containing theC2h-symmetric terphenyl-based dicarboxylate linker 1,1′:4′,1′′-terphenyl-3,3′-dicarboxylate (3,3′-TPDC), namelycatena-poly[[bis(dimethylamine-κN)copper(II)]-μ-1,1′:4′,1′′-terphenyl-3,3′-dicarboxylato-κ4O,O′:O′′:O′′′] monohydrate], {[Cu(C20H12O4)(C2H7N)2]·H2O}n, (I), andcatena-poly[[aquabis(dimethylamine-κN)copper(II)]-μ-1,1′:4′,1′′-terphenyl-3,3′-dicarboxylato-κ2O3:O3′] monohydrate], {[Cu(C20H12O4)(C2H7N)2(H2O)]·H2O}n, (II), were both obtained from two different methods of preparation: one reaction was performed in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO) as a potential pillar ligand and the other was carried out in the absence of the DABCO pillar. Both reactions afforded crystals of different colours,i.e.violet plates for (I) and blue needles for (II), both of which were analysed by X-ray crystallography. The 3,3′-TPDC bridging ligands coordinate the CuIIions in asymmetric chelating modes in (I) and in monodenate binding modes in (II), forming one-dimensional chains in each case. Both coordination polymers contain two coordinated dimethylamine ligands in mutuallytranspositions, and there is an additional aqua ligand in (II). The solvent water molecules are involved in hydrogen bonds between the one-dimensional coordination polymer chains, forming a two-dimensional network in (I) and a three-dimensional network in (II).


2017 ◽  
Vol 656 (1) ◽  
pp. 96-104 ◽  
Author(s):  
Osamu Haba ◽  
Wataru Matsuno ◽  
Nao Nakamura ◽  
Hiroshi Awano ◽  
Tatsuhiro Takahashi ◽  
...  

1999 ◽  
Vol 32 (26) ◽  
pp. 8829-8835 ◽  
Author(s):  
Yiliang Wu ◽  
Jun-ichi Mamiya ◽  
Akihiko Kanazawa ◽  
Takeshi Shiono ◽  
Tomiki Ikeda ◽  
...  

2012 ◽  
Vol 554-556 ◽  
pp. 807-810 ◽  
Author(s):  
Ying Gang Jia ◽  
Kun Ming Song ◽  
Bao Yan Zhang

The synthesis of new side chain cholesteric liquid crystalline elastomers (ChLCEs) containing the cholesteric monomer M and the flexible non-mesogenic crosslinking agent C, is described. The selective reflection of light for M was characterized with UV/Visible/NIR. The phase behavior and mesomorphism were investigated by differential scanning calorimetry (DSC), polarizing optical microscopy (POM), and X-ray diffraction (XRD). The effect of the content of crosslinking units on the phase behavior and mesomorphism of elastomers P1– P8is discussed. The ChLCEs exhibit elasticity, reversible phase transitions, and cholesteric Grandjean texture. The experimental results demonstrate that the glass transition temperature and isotropic temperature of ChLCEs decrease with increasing the content of crosslinking unit, but the cholesteric phase is not disturbed.


1990 ◽  
Vol 23 (23) ◽  
pp. 5020-5024 ◽  
Author(s):  
Gilles Sigaud ◽  
M. F. Achard ◽  
F. Hardouin ◽  
C. Coulon ◽  
H. Richard ◽  
...  

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