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Self-assembly and UV-curing Property of Polymerized Lyotropic Liquid Crystal Monomer of Sodium 3,4,5-tris(ll-acryloxyundecyloxy)benzoate 被引量:1

可聚合型溶致液晶单体3,4,5.三(11-十一烷氧丙烯酰氧基)苯甲酸钠的自组装及紫外光固化性能
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摘要 A polymerized lyotropic liquid crystal monomer of sodium 3,4,5-tris(11-acryloxyundecyloxy)- benzoate was synthesized by a convenient route starting from 3,4,5-trihydroxybenzoic acid via esterification followed by etherification, acylation and finally neutralization. The chemi- cal structure was confirmed by Fourier transform infrared (FT-IR) and 1H nuclear magnetic resonance spectral analysis. The self-organization behavior of the monomer with deionized water in methanol at room temperature was also demonstrated. The assemblies were char- acterized by polarized optical microscope and X-ray diffraction. The results show that a solution containing 80:20 of the monomer to water was found to be able to self-organize into Lamellar (La) phase and 92:8 with inverted hexagonal (H]I) phase, which was in ac- cordance with the theoretical calculation of critical packing parameter. It suggests that the concentration of the monomer was the key factor to influence assembly structure. Addi- tionally, the acrylate conversion with different photoinitiators and nanostructure retention after polymerization were investigated. The research shows that the acrylate conversion of the monomer with Darocur2959 could reach up to 78% when irradiated by 30 mW/cm2 UV light of 365 nm for 30 min characterized by Real-time FT-IR as well as the sol-gel method. Meanwhile, the La and HII phase nanostructures were both retained after polymerization.
出处 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2013年第1期95-101,I0004,共8页 化学物理学报(英文)
关键词 Polymerized lyotropic liquid crystal SELF-ASSEMBLY La phase HII phase UV-CURING 可聚合型溶致液晶,自组装,层状相,反六方相,紫外光固化
分类号 O [理学]
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  • 1D. L. Gin, W. Q. Gu, B. A. Pindzola, and W. J. Zhou Acc. Chem. Res. 34, 973 (2001).
  • 2R. J. Guo, B. Q. Zhang, Y. Sun, and X. F. Liu, Prog Chem. 19, 1695 (2007).
  • 3D. L. Gin, J. E. Bara, R. D. Noble, and B. J. Elliott Macromol. Rapid Commun. 29, 367 (2008).
  • 4A. L. Lafrate, J. E. Bara, D. L. Gin, and R. D. Noble Ind. Eng. Chem. Res. 48, 8757 (2009).
  • 5J. E. Bara, D. E. Camper, D. L. Gin, and R. D. Noble Ace. Chem. Res. 43, 152 (2010).
  • 6A. L. Lafrate, D. L. Gin, and R. D. Noble, Ind. Eng Chem. Res. (2010).
  • 7J. E. Bara, S. Lessmann, C. J. Gabriel, E. S Hatakeyama, R. D. Noble, and D. L. Gin, Ind. Eng Chem. Res. 46, 5397 (2007).
  • 8E. S. Hatakeyama, C. J. Gabriel, B. R. Wiesenauer, J L. Lohr, M. J. Zhou, R. D. Noble, and D. L. Gin, J Membr. Sci. (2010).
  • 9P. V. Braun, P. Osenar, M. Twardowski, G. N. Tew and S. I. Stupp, Adv. Funct. Mater. 15, 1745 (2005).
  • 10Y. Yamauchi, T. Momma, M. Fuziwara, S. S. Nair, T Ohsuna, O. Terasaki, T. Osaka, and K. Kuroda. Chem Mater. 17, 6342 (2005).

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