Ion-controlled switchable progress is very important in many biological behaviors. Here, we reported K(+)-controlled switch, this switch system exhibited excellent carbaryl (G) binding/release by fluorescent (FL), ultraviolet-visible (UV) spectrums and (1)H NMR spectroscopy. More importantly, the K(+)-controlled G binding/release switch based on C4C5 not only in the solution, but also on the surface, promising for the application for the pesticide controlled release.
View Article and Find Full Text PDFA new fluorescent dianthracene calix[4]arene (C4DA) was designed and synthesized via coupling the fluorescent anthracene units and calix[4]arene units. Then it was used to form self-assembled monolayers (C4DA-SAMs) by the simple click reaction to give the first fluorescent and wettable dual-signal switch for tryptophan (Trp) on a micro- and nano-structured silicon surface. The switch for Trp on the C4DA functional surface was confirmed by contact angle (CA) measurements and fluorescent spectroscopy (FL).
View Article and Find Full Text PDFThe recognition of the mercury(II) ion (Hg(2+)) is essential because of its extreme toxicity in the environment and food. Hence we reported a novel cysteine (Cys) complex of piperidine-calix[4]arene (L) as a convenient and effective dual-signal responsive switch for Hg(2+). This switch system exhibited excellent selectivity toward Hg(2+) by fluorescence (FL), (1)H NMR spectroscopy and the atomic force microscopy (AFM).
View Article and Find Full Text PDFA new calix[4]azacrown is synthesized from 1,3-dipropynyloxycalix[4]arene in a good yield of 85% and was modified on a silicon surface via click chemistry to be a switchable wettability sensor for ion pairs ([C(4)mim]Cl). A cooperative mechanism involving supramolecular interactions is proposed.
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