Controlled Self-Assembly-Synthetic Tunability and Covalent Capture of Nanoscale Gel Morphologies

被引:33
作者
Coates, Ian A. [1 ]
Smith, David K. [1 ]
机构
[1] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
gels; metathesis; nanochemistry; self-assembly; supramolecular chemistry; GELATORS; ORGANOGELATOR; CONFORMATION; POLYMERS; DESIGN; ACID;
D O I
10.1002/chem.200900858
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A synthetically simple gelator with the capacity to be crosslinked, leading to the covalent capture of the different nano-assemblies was demonstrated. The gelator was assembled through self-complementary hydrogen bond interactions to yield two completely different nanoscale morphologies under different cooling conditions. Lysine bis-urea was synthesized in high yield by a simple one-step synthesis and by mixing two commercially available chemicals, lysine di-isocyanate and allylamine. It was observed that the different self-assembled structures could be covalently 'captured' by alkene metathesis. It was also found that the morphologies of the self-assembled nanoscale structures could be tuned in response to sample cooling rates. Double bonds of the gelator allowed the self-assembled structures to be captured by covalent cross-linking yielding solid and robust nanostructured materials.
引用
收藏
页码:6340 / 6344
页数:5
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