Self-assembly of vesicles from amphiphilic aromatic amide-based oligomers

A novel class of linear arylamide oligomers has been designed and synthesized from naphthalene-2,7-diamine and benzene-1,3,5-tricarboxylic acid segments. The molecules carry two (tert-butoxycarbonylamino) groups at the ends and one to three hydrophilic N,N-bis(2-(2-(2-methoxyethoxy)ethoxy)ethyl)amin...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1991. - 25(2009), 5 vom: 03. März, Seite 2684-8
1. Verfasser: Xu, Yun-Xiang (VerfasserIn)
Weitere Verfasser: Wang, Gui-Tao, Zhao, Xin, Jiang, Xi-Kui, Li, Zhan-Ting
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Amides Polymers Solvents DNA 9007-49-2 Methanol Y4S76JWI15
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520 |a A novel class of linear arylamide oligomers has been designed and synthesized from naphthalene-2,7-diamine and benzene-1,3,5-tricarboxylic acid segments. The molecules carry two (tert-butoxycarbonylamino) groups at the ends and one to three hydrophilic N,N-bis(2-(2-(2-methoxyethoxy)ethoxy)ethyl)amino groups at one side of the backbone. The oligomers self-assembled into vesicular structures in methanol as a result of ordered stacking of the oligomeric amide backbones, which were evidenced by SEM, AFM, TEM, and fluorescent micrography experiments. It was also found that the tert-butoxycarbonylamino groups at the ends played an important role in promoting the ordered stacking of the backbones. Structural factors that affected the self-assembly of the oligomers were investigated. A two-layer model that was supported by TEM has been proposed for the formation of the vesicular structures, which was driven by both the hydrogen bonding and aromatic stacking 
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700 1 |a Zhao, Xin  |e verfasserin  |4 aut 
700 1 |a Jiang, Xi-Kui  |e verfasserin  |4 aut 
700 1 |a Li, Zhan-Ting  |e verfasserin  |4 aut 
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