Synthesis and photoresponsive properties of two liquid crystalline polymers bearing branched azobenzene-containing side chains
文献信息
Yu Zhu, Xiaogong Wang
We synthesized two photoresponsive liquid crystalline polymers bearing branched azobenzene-containing side-chains. The side-chain liquid crystal polymers (SCLCPs) were designed to contain two and three azobenzene moieties in each monomeric unit, which were attached to the backbones via a linkage of biphenylene and flexible spacers. The SCLCPs were synthesized by radical polymerization of corresponding methacrylate-based monomers. The polymers were characterized by FT-IR, 1H NMR, UV-vis, GPC and small angle X-ray scattering (SAXS). Both polymers formed the smectic-A mesophase in the LC states, whilst the polymer containing three azobenzene-containing branches in each repeat unit showed a high order mesophase in the lower temperature range. The polymers exhibited trans–cis photoisomerization and photoinduced orientation under light irradiation at suitable wavelengths.
相关文献
Photomanipulation of the anchoring strength using a spontaneously adsorbed layer of azo dendrimers
Hajnalka Nádasi, Ralf Stannarius, Alexey Eremin, Ken Ishikawa, Osamu Haba, Koichiro Yonetake, Hideo Takezoe, Fumito Araoka
DOI: 10.1039/C6CP08461C
Anisotropic carrier mobility in buckled two-dimensional GaN
Lijia Tong, Junjie He, Min Yang, Zheng Chen, Jing Zhang, Yanli Lu, Ziyuan Zhao
DOI: 10.1039/C7CP04117A
Retraction: Facile synthesis of hierarchical Mn3O4 superstructures and efficient catalytic performance
DOI: 10.1039/C7CP90191G
Pd-P nanoparticles supported on PxOy-incorporated carbon nanotubes for enhanced methanol oxidation in an alkaline medium
Yanan Xie, Weizhen Yu, Juan Wang, Yifei Wu, Shuo Niu, Wenyao Guo, Tsungwu Lin, Lidong Shao
DOI: 10.1039/C7CP04540A
Temperature dependence of ion diffusion coefficients in NaCl electrolyte confined within graphene nanochannels
Jing Kong, Zheng Bo, Huachao Yang, Jinyuan Yang, Xiaorui Shuai, Jianhua Yan, Kefa Cen
DOI: 10.1039/C6CP08752C
Transdermal cellular membrane penetration of proteins with gold nanoparticles: a molecular dynamics study
Rakesh Gupta, Nishi Kashyap, Beena Rai
DOI: 10.1039/C6CP08775B
First principles study of oxygen molecule interaction with the graphitic active sites of a boron-doped pyrolyzed Fe–N–C catalyst
Febdian Rusydi
DOI: 10.1039/C7CP02390A
Probing the charge distribution at the electrochemical interface
Yvonne Gründer, Christopher A. Lucas
DOI: 10.1039/C7CP00244K
Density functional study on the resistance to sulfur poisoning of Ptx (x = 0, 1, 4 and 8) modified α-Mo2C(0001) surfaces
Weimeng Kong, Xilin Zhang, Jianjun Mao, Xiaopei Xu, Yanxing Zhang
DOI: 10.1039/C7CP04718E
您可能还喜欢
(3-氨苯基)环丙基甲酮(CAS号:162174-75-6)的主要用途是什么?
(3-氨苯基)环丙基甲酮主要用于合成化学中间体,特别是在药物化学领域作为原料。它还可以用于有机合成反应中,作为催化剂或反应物。
如何储存亚胺菌(CAS号:136470-79-6)?
亚胺菌应储存在干燥、阴凉处,避免直接暴露于光线下。建议使用密封容器储存,防止吸潮和污染。具体的储存条件应参考产品的安全数据表(MSDS)或药品说明书。
2-氯-2,2-二氟乙酰胺(CAS号:354-28-9)应用于哪些行业?
2-氯-2,2-二氟乙酰胺在医药、聚合物、传感器、半导体等领域有广泛应用。在医药领域,它作为中间体用于合成其他药物;在聚合物领域,用作聚合引发剂或稳定剂;在传感...
处理4-甲基-3-硝基-1,1-联苯(CAS号:53812-68-3)时应注意哪些实验室安全事项?
在处理4-甲基-3-硝基-1,1-联苯时,应佩戴手套、护目镜和实验室外套等个人防护装备(PPE),确保在通风橱中操作以减少吸入风险。若发生泄露,应立即使用沙子或...
(2S)-羟基(苯基)乙酸 (2R)-N-苄基-1-(4-甲氧基苯基)丙-2-胺盐(CAS号:188690-84-8)应用于哪些行业?
该化合物广泛应用于医药、聚合物和半导体行业。在医药领域,它是某些药物中间体的重要组成部分;在聚合物领域,可用作增塑剂;在半导体行业,可用于制造光刻胶。
在合成中是否有芬苯哒唑砜-D3标准品(CAS号:1228182-49-7)的替代品?
芬苯哒唑砜-D3标准品的替代品可能包括类似的苯并咪唑类化合物,如芬苯哒唑本身或其非同位素标记版本。这些替代品在结构上与芬苯哒唑砜-D3相似,但在具体应用中需进行...
2-氟-4-硝基苯乙酸(CAS号:315228-19-4)通常如何合成?
2-氟-4-硝基苯乙酸可以通过一系列化学反应合成,通常是从4-氟苯胺开始,首先进行硝化反应生成4-氟-2-硝基苯胺,然后进行乙酰化反应得到目标产物。具体的合成步...
2-氟-4-甲氧基苯乙酸(CAS号:883531-28-0)通常如何合成?
2-氟-4-甲氧基苯乙酸通常通过将4-甲氧基苯乙酸与氟化试剂(如氟化氰)反应来合成。反应通常在无水条件下进行,使用催化剂如六氟磷酸锂或四氟硼酸锂以提高选择性和产...
什么是4SC 202;4SC202(CAS号:1186222-89-8)?
4SC 202;4SC202是一种化学化合物,其化学名称为(2E)-N-(2-氨基苯基)-3-(1-{[4-(1-甲基-1H-吡唑-4-基)苯基]磺酰基}-1H...
来源期刊
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.










![4-[(2,4-Dihydroxyphenyl)diazenyl]-5-hydroxy-2,7-naphthalenedisulfonic acid structure 4-[(2,4-Dihydroxyphenyl)diazenyl]-5-hydroxy-2,7-naphthalenedisulfonic acid structure](https://cnstatic.chemtradehub.com/structs/362/3627-01-8-79ac.webp)



![(2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure (2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure](https://cnstatic.chemtradehub.com/structs/173/173867-04-4-d2d3.webp)