期刊文献+

基于聚环氧乙烷链和亚苯基的刚棒-线团分子自组装 被引量:5

Self-Assembly of Rod-Coil Molecules with Poly (ethylene oxide) Chains and Phenylene Rods
原文传递
导出
摘要 含有亲水性聚环氧乙烷(PEO)链和多个亚苯基作为刚棒的刚棒-线团(rod-coil)分子,由于具有很强的π-π堆积作用和微相分离作用,可以在本体和溶液中产生有序排列形成各种组装体。材料的性能主要依靠分子聚集体来体现,因此研究分子聚集体的性质和用途成为当前超分子领域研究的重要内容。刚棒嵌段的形状影响着分子排列的方式、自组织性能和微结构,本文总结了Y型、T型、O型、K型、n型、螺旋桨型和哑铃型等不同形状分子的自组装行为,并展望了此类刚棒-线团分子未来研究的方向。 The rod-coil molecules, containing the hydrophilic poly(ethylene oxide) (PEO) chains and multiphenylene as a rod, are able to self-assemble into various supramoleeular nanostruetures in bulk and an aqueous solution, caused by strong π-π stacking of aromatic rod segments and mierophase separation of rod and coil segments. One of the great fascinating research topics is the creation of supramoleeular nano-objects to explore novel properties and functions of rod-coil molecules. The shapes of the rod block can dramatically influence on the fashion of molecular arrangement, self-organizing property and micro-structure of rod-coil molecular system. In this paper, the self-assembling behaviors of diverse rod-coil molecules are summarized including Y-shaped, T-shaped, O-shaped, K-shaped, n-shaped, propeller-like and dumbbell-like rods. Finally, the future research trend of this kind of rod-coil molecules is prospected.
出处 《化学进展》 SCIE CAS CSCD 北大核心 2012年第7期1353-1358,共6页 Progress in Chemistry
基金 国家自然科学基金项目(No.21164013) 吉林省自然科学基金面上项目(No.201115225) 辽宁省食品安全重点实验室暨辽宁省高校重大科技平台"食品贮藏加工及质量安全控制工程技术研究中心"开放课题(LNSAKF2011024)资助
关键词 刚棒-线团分子 自组装 超分子 形状 rod-coil molecules self-assembly supramoleeule shape
  • 相关文献

参考文献42

  • 1Claessens C G, Stoddart J F. J. Phys. Org. Chem. , 1997, 10 (5) : 254-272.
  • 2Gillard R E, Raymo F M, Stoddart J F. Chem. Eur. J. , 1997, 3(12) : 1933-1940.
  • 3De Mendoza J. Chem. Eur. J. , 1998, 4(8) : 1373-I377.
  • 4Kato T, Mizoshita N, Kanie K. Macromol. Rapid. Commun. , 2001, 22(11) : 797-814.
  • 5Prins L J, Reinhoudt D N, Timmerman P. Angew. Chem. Int. Ed. , 2001, 40(13): 2382-2426.
  • 6QiW, LiH L, WuLX. Adv. Mater. ,2007, 19(15): 1983- 1987.
  • 7Zhang J, Zhou M J, Wang S, Carr J, Li W, Wa L X. Langmuir, 2011, 27(7) : 4134-4141.
  • 8Wang H B, Yan Y, Li B, Bi L H, Wu L X. Chem. Eur. J. , 2011, 17(15) : 4273-4282.
  • 9Kato T, Yasuda T, Kamikawa Y, Yoshio M. Chem. Commun. , 2009, 729-739.
  • 10Lehn J M. Angew. Chem. Int. Ed. , 1990, 29(11): 1304- 1319.

同被引文献79

  • 1Shimizu T, Masuda M, Minamikawa H. Supramo- lecular nanotube architectures based on amphiphilic molecules[J]. Chem Rev, 2005,105 : 1401 1443.
  • 2Rosi N L, Mirkin C A. Nanostructures in biodiag- nostics[J]. Chem Rev, 2005,105 : 1547-1562.
  • 3Lim Y B, Moon K S, Lee M. Recent advances in functional supramolecular nanostructures assembled from bioactive building blocks[J]. Chem Soc Rev, 2009,38:925-934.
  • 4Cavalli S, Albericio F, Kros A. Amphiphilic peptides and their crosdisciplinary role as building blocks for nanoscience[J]. Chem Soc Rev, 2010,39:241-263.
  • 5Hentschel J. Making "smart polymers" smarter: mod- em concepts to regulate functions in polymer science[J]. J Polym Sci Part A: Polym Chem, 2010,48:1-14.
  • 6Klajn R, Stoddart J F, Grzybowski B A. Nanopar- ticles functionalized with reversible molecular and supramoleeular switches[J]. Chem Soe Rev, 2010, 39:2203-2237.
  • 7Ajayaghosh A, Praveen V K. -Organogels of sel assembled p-phenylenevinylenes., soft materials with distinct size, shape, and funetions[J] Acc Chem Res, 2007,40:644-656.
  • 8Pennadam S, Alexander C. Stimuli responsive poly- mers for biomedical applications [J]. Chem Soc Rev, 2005,34:276 285.
  • 9Mendes P M. Stimuli-responsive surfaces for bio-appli- cations[J]. Chem Soe Rev, 2008,37:2512-2529.
  • 10Yagai S, Kitamura A. Recent advances in photore- sponsive supramoleeular self-assemblies[J]. Chem Soc Rev, 2008,371520-1529.

引证文献5

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部