Self-assembly and characterization of hydrogen-bond-induced nanostructure aggregation

被引:40
作者
Liu, Y [1 ]
Zhuang, JP
Liu, HB
Li, YL
Lu, FS
Gan, HY
Jiu, TG
Wang, N
He, XR
Zhu, DB
机构
[1] Chinese Acad Sci, CAS Key Lab Organ Solids, Ctr Mol Sci, Inst Chem, Beijing 100080, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100864, Peoples R China
关键词
aggregation; hydrogen bonds; nanostructures; perylene bisimides; self-assembly;
D O I
10.1002/cphc.200400165
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A supramolecular system of a perylene derivative containing bis(2,6-diacylaminopyridine) units and a perylene bisimide bound through three hydrogen-bonds was synthesized and characterized. H-1 NMR spectra confirmed the existence of hydrogen-bonding interactions between the perylene derivative (3) and the perylene bisimide (7). The photocurrent generation of the self-assembled 3.7 film was measured, and a cathodic photocurrent response was obtained. SEM images indicated that well-defined long fibers could be fabricated by self-assembly, by exploiting the hydrogen bonding interactions and pi-pi stacking interactions of perylene rings.
引用
收藏
页码:1210 / 1215
页数:6
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