2006
DOI: 10.1021/ac061481t
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Decolorization of Ionic Liquids for Spectroscopy

Abstract: It has been widely recognized that although ionic liquids should be colorless, they are frequently not. Colored samples appear to be pure by most analytical techniques (e.g., NMR spectroscopy, mass spectrometry, HPLC, and ion chromatography), and there have been many attempts to identify the source of color in our own laboratories and others-after 20 years the best that can be said is that the impurities are at a very low level (probably parts per billion) with very high molar extinction coefficients. In this … Show more

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Cited by 184 publications
(117 citation statements)
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“…We will show in the present study that the C dc behavior at the IL«EGaIn interface measured using the pendant drop method reproduces that at the IL«Hg interface, supporting that the phenomena observed at the IL«Hg interface are universal for the EDL in ILs. 30,76 Before measurements, volatile impurities were removed from the ILs by using a rotary oil pump for more than 3 h at 60°C. EGaIn (99.99%, Alfa Aesar) was stored in an 1 M HCl aqueous solution.…”
Section: Introductionmentioning
confidence: 99%
“…We will show in the present study that the C dc behavior at the IL«EGaIn interface measured using the pendant drop method reproduces that at the IL«Hg interface, supporting that the phenomena observed at the IL«Hg interface are universal for the EDL in ILs. 30,76 Before measurements, volatile impurities were removed from the ILs by using a rotary oil pump for more than 3 h at 60°C. EGaIn (99.99%, Alfa Aesar) was stored in an 1 M HCl aqueous solution.…”
Section: Introductionmentioning
confidence: 99%
“…17 Hence, they are being actively investigated as alternative solvent media in synthesis, 18 catalysis, 19 polymerization, [20][21][22] separation, 23 electrochemistry 24,25 and electrochemical devices. 26,27 However, the basic science involved with fully characterizing these ILs is still in its infancy, and this may be holding back the complete and most efficient utilization of these potentially, and only in some cases, 28 41 dried under vacuum at 40 1C for 48 h, and stored under argon at 20 1C before analysis. Absorption spectra were recorded on a Varian Cary 100 Bio UV-Visible Spectrophotometer, this instrument is also equipped with a temperature-controlled 6 Â 6 multicell holder.…”
Section: Introductionmentioning
confidence: 99%
“…59 The synthesis of the other ionic liquids shown in Figure 1 is described elsewhere, 11,60,61 and they were decolorized according to the procedure described previously. 62 Briefly, the impure ionic liquid was diluted and was allowed to elute through a column packed with celite, silica gel, and activated charcoal. After the excess solvent was removed, the ionic liquid was dried under vacuum with mild heating.…”
Section: à48mentioning
confidence: 99%