Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5219250 | Tetrahedron | 2012 | 4 Pages |
Abstract
Novel naphthyl-modified calix[4]arene was synthesized by click chemistry, and exhibited high affinity and selectivity for p-nitroaniline by the fluorescence spectroscopy. However, the sensitivity toward other anilines 3a-e are negligible. The 1H NMR, 1H NOESY, MALDI-TOF mass spectroscopy and computational calculations revealed the formation of host-guest complex driven by H-bonding and hydrophobic interactions.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Junyan Zhan, Xiaolei Zhu, Fei Fang, Fajun Miao, Demei Tian, Haibing Li,