Pronounced effects of cross-linker geometries on the orientation coupling between dangling mesogens and network backbones in side-chain type liquid crystal elastomers
Pronounced effects of cross-linker geometries on the orientation coupling between dangling mesogens and network backbones in side-chain type liquid crystal elastomers
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DOI:
10.1016/j.polymer.2015.01.069
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发表时间:
2015-03
期刊:
影响因子:
4.6
通讯作者:
Akane Tsuchitani;Haruhisa Ashida;K. Urayama
中科院分区:
文献类型:
--
作者:
Akane Tsuchitani;Haruhisa Ashida;K. Urayama
We demonstrate that the cross-linker geometries such as molecular length and functionality have a pronounced effect on the orientation coupling between the dangling mesogens and network backbones in the side-chain type liquid crystal elastomers which are made by the copolymerization of mono-functional mesogens and multi-functional non-mesogenic cross-linkers. For the nematic elastomers (NEs) with planar alignment, the cooling causes an increase in nematic order of the dangling mesogens independently of the cross-linker geometries. Correspondingly, a finite macroscopic elongation along the director is induced for the NEs with the bi-functional (F= 2) and sufficiently long cross-linkers withN≥ 6 (N; the number of methylene units between the functional groups), but no macroscopic deformation is driven for the NEs with the short cross-linkers withN≤ 4 independently ofF. When the corresponding NEs with polydomain alignment are stretched by externally imposed strain, the dangling mesogens are reoriented along the stretching direction independently ofNin the case ofF= 2 whereas no reorientation of the mesogens is driven in the cases of the short tri- and tetra-functional cross-linkers (N= 3 andF= 3, 4). Such striking and complicated effects of the cross-linker geometries on the orientation-coupling between the dangling mesogens and network backbones is expected from the heterogeneous network structure composed of the dense and sparse regions of cross-links which are characteristic of the polymer networks formed by the copolymerization of mono- and multi-functional monomers.