2008
DOI: 10.1039/b716889f
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Ionic liquids as novel guests for cucurbit[6]uril in neutral water

Abstract: Cucurbit[6]uril was dissolved through encapsulation of an imidazolium-based ionic liquid guest in a pure water environment and the dissolution ability could be tuned by augmenting the imidazolium structure.

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Cited by 54 publications
(43 citation statements)
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“…The reactions of amines with CO 2 in water for a long time are inclined to form bicarbonate as primary product, however the conversions are hardly complete with a little side product of carbamate, for they are equilibrium reactions. In our model experiment, NH 2 (CH 2 ) 6 NH 2 reacted with CO 2 in aqueous solution, leading to carbamate product first and then bicarbonate, which were demonstrated by the appearance of carbonyl signals on 13 C NMR spectra at δ 164.5 and 159.9 ppm, respectively.…”
Section: Resultsmentioning
confidence: 99%
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“…The reactions of amines with CO 2 in water for a long time are inclined to form bicarbonate as primary product, however the conversions are hardly complete with a little side product of carbamate, for they are equilibrium reactions. In our model experiment, NH 2 (CH 2 ) 6 NH 2 reacted with CO 2 in aqueous solution, leading to carbamate product first and then bicarbonate, which were demonstrated by the appearance of carbonyl signals on 13 C NMR spectra at δ 164.5 and 159.9 ppm, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…For reaction of NH 2 (CH 2 ) 6 NH 2 CB [7] complex with CO 2 in aqueous solution, the new resonance signal on 13 C NMR spectrum at δ 159.8 ppm was assigned to bicarbonate as the only product of CO 2 fixation, while carbamate product was not detected.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The interaction of CB6 and [C n mim]Br was found to significantly increase the solubility of CB6 in neutral water . CB6 was pulled into neutral water through encapsulation of an imidazolium-based IL (Liu et al, 2008). According to 1 H NMR titration experiments, C 2 mim + and C 4 mim + demonstrated different binding modes with CB6.…”
Section: Fig 3 Two-mentioning
confidence: 99%
“…Accordingly, we can design a fluorescent chemosensor for fluoride anions. In general, free imidazolium do not have visible light absorption [20][21][22][23]. To improve the photoabsorption properties of imidazolium cations, some groups with conjugated structures can be introduced into the imidazolium skeleton [24,25].…”
Section: Introductionmentioning
confidence: 99%