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Controlling the self-assembly of cationic bolaamphiphiles: counterion-directed transitions from 0D/1D to exclusively 2D planar structures
被引:36
作者:
Wu, Guanglu
[1
]
Verwilst, Peter
[2
]
Liu, Kai
[1
]
Smet, Mario
[2
]
Faul, Charl F. J.
[3
]
Zhang, Xi
[1
]
机构:
[1] Tsinghua Univ, Dept Chem, Key Lab Organ Optoelect & Mol Engn, Beijing 100084, Peoples R China
[2] Katholieke Univ Leuven, Dept Chem, B-3001 Louvain, Belgium
[3] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
关键词:
ALKYLPYRIDINIUM SURFACTANTS;
AQUEOUS-SOLUTION;
MICELLES;
AMPHIPHILES;
ORGANIZATION;
WATER;
NANOSTRUCTURES;
ARCHITECTURES;
HEADGROUPS;
NANOSHEETS;
D O I:
10.1039/c3sc52342j
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Self-assembly of cationic bolaamphiphiles is usually reported to form one-dimensional (1D) or zerodimensional (0D), rather than two-dimensional (2D) structures. Here we have found a facile counteriondirected structure switch for such amphiphilic moieties. 0D/1D structures formed by self-assembly of cationic bolaamphiphiles can be converted into 2D planar structures by a simple counterion change to tosylate. As indicated by the single crystal structure and variable-temperature NMR studies, the strong binding between tosylate counterions and cationic headgroups drives the formation of 2D planar structures. It is highly anticipated that this approach may present as a simple methodology to control the stacking of the embedded conjugated cores in bolaamphiphiles, therefore modulating optoelectronic properties and function in such assemblies.
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页码:4486 / 4493
页数:8
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