期刊
CHEMICAL COMMUNICATIONS
卷 -, 期 30, 页码 3196-3198出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b606371c
关键词
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Intertwining triple helical nanofibers with an overall handedness have been formed from self-assembling chiral benzene-1,3,5-tricarboxamides 1, 2 and 3, whereas the achiralbenzene-1,3,5-tricarboxamide 4 upon self-association gives rise to straight nanofibers without any twist and transmission electron microscopy images of chiral compounds clearly demonstrate that the handedness of the triple helical nanofibers can be reversed by using the enantiomeric benzene-1,3,5-tricarboxamide building blocks.
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