首页 | 本学科首页   官方微博 | 高级检索  
     检索      

一种新型偶氮聚电解质的光致取向行为研究
引用本文:邓永红,和亚宁,焉学佳,漆海波,王晓工.一种新型偶氮聚电解质的光致取向行为研究[J].高分子学报,2004(2):299-303.
作者姓名:邓永红  和亚宁  焉学佳  漆海波  王晓工
作者单位:清华大学材料科学与工程研究院,化工系高分子研究所,北京,100084
基金项目:国家自然科学基金资助项目(基金号59925309)
摘    要:1992年Decher等报道了聚电解质的静电逐层自组装技术,即将带有相反电荷的两种聚电解质通过交替沉积的方式,在固体介质表面上形成均匀的厚度可控的多层膜。利用此方法可方便地对膜结构进行设计和调控,从原理上讲,可制备任意成分多层复合的新材料。该技术以其操作简易,结构可控等特点已成为近10年功能高分子纳米薄膜领域的研究热点。

关 键 词:偶氮聚电解质  自组装  H-聚集  光致取向
修稿时间:2003年7月28日

LAYER-BY-LAYER SELF-ASSEMBLY AND PHOTO-INDUCED DICHROISM OF A NOVEL SIDE-CHAIN AZO POLYELECTROLYTE
DENG Yonghong,He Yaning,Yan Xuejia,Qi Haibo,WANG Xiaogong.LAYER-BY-LAYER SELF-ASSEMBLY AND PHOTO-INDUCED DICHROISM OF A NOVEL SIDE-CHAIN AZO POLYELECTROLYTE[J].Acta Polymerica Sinica,2004(2):299-303.
Authors:DENG Yonghong  He Yaning  Yan Xuejia  Qi Haibo  WANG Xiaogong
Abstract:A novel polyelectrolyte PNANT functionalized with electron donor-acceptor type azobenzene chromophores has been synthesized through post-polymerization azo coupling reaction and characterized by 1H-NMR,FTIR and UV-Vis spectroscopy.The degree of functionalization (DF) of PNANT was 20% measured by elemental analysis.The degree of polymerization and its distribution were determined by GPC to be X n=251 with a polydispersion index 1.53.A glass transition temperature of 119℃ was observed from DSC thermogram. H-aggregation of azo chromophores of PNANT in spin-coated film and self-assembled film were detected from UV-Vis spectra,and the degree of H-aggregation of PNANT in the self-assembled film was found to be higher than that in the spin-coated film.Dichroism was optically induced in the spin-coated film and self-assembled film upon the irradiation of a polarized Ar + laser beam at 488 nm.The orientational order parameter obtained was 0.15 for spin-coated film and 0.07 for the self-assembled film.The resulting dichroism detected by UV-Vis spectra exhibited long-term stability.
Keywords:Azo polyelectrolyte  Self-assembled multilayers  H-aggregation  Dichroism  
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号