Real-Time 2D NMR Identification of Analytes Undergoing Continuous Chromatographic Separation
We have recently proposed and demonstrated an approach that enables the acquisition of multidimensional nuclear magnetic resonance (NMR) spectra within a single scan. A promising application opened up by this new accelerated form of data acquisition concerns the possibility of monitoring in real tim...
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Published in | Journal of the American Chemical Society Vol. 126; no. 4; pp. 1262 - 1265 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Chemical Society
04.02.2004
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Abstract | We have recently proposed and demonstrated an approach that enables the acquisition of multidimensional nuclear magnetic resonance (NMR) spectra within a single scan. A promising application opened up by this new accelerated form of data acquisition concerns the possibility of monitoring in real time the chemical nature of analytes subject to a continuous flow. The present paper illustrates such potential, with the real-time acquisition of a series of 2D 1H NMR spectra arising from a mixture of compounds subject to a continuous liquid chromatography (LC) separation. This real-time 2D NMR identification of chemicals eluted minutes apart under usual LC−NMR conditions differs from the way in which LC−2D NMR has hitherto been carried out, which relies on stopped-flow modes of operations whereby fractions are first collected and then subject to individual, aliquot-by-aliquot analyses. The real-time LC−2D NMR experiment hereby introduced can be implemented in a straightforward manner using modern commercial LC−NMR hardware, thus opening up immediate possibilities in high-throughput characterizations of complex molecules. |
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AbstractList | We have recently proposed and demonstrated an approach that enables the acquisition of multidimensional nuclear magnetic resonance (NMR) spectra within a single scan. A promising application opened up by this new accelerated form of data acquisition concerns the possibility of monitoring in real time the chemical nature of analytes subject to a continuous flow. The present paper illustrates such potential, with the real-time acquisition of a series of 2D 1H NMR spectra arising from a mixture of compounds subject to a continuous liquid chromatography (LC) separation. This real-time 2D NMR identification of chemicals eluted minutes apart under usual LC-NMR conditions differs from the way in which LC-2D NMR has hitherto been carried out, which relies on stopped-flow modes of operations whereby fractions are first collected and then subject to individual, aliquot-by-aliquot analyses. The real-time LC-2D NMR experiment hereby introduced can be implemented in a straightforward manner using modern commercial LC-NMR hardware, thus opening up immediate possibilities in high-throughput characterizations of complex molecules.We have recently proposed and demonstrated an approach that enables the acquisition of multidimensional nuclear magnetic resonance (NMR) spectra within a single scan. A promising application opened up by this new accelerated form of data acquisition concerns the possibility of monitoring in real time the chemical nature of analytes subject to a continuous flow. The present paper illustrates such potential, with the real-time acquisition of a series of 2D 1H NMR spectra arising from a mixture of compounds subject to a continuous liquid chromatography (LC) separation. This real-time 2D NMR identification of chemicals eluted minutes apart under usual LC-NMR conditions differs from the way in which LC-2D NMR has hitherto been carried out, which relies on stopped-flow modes of operations whereby fractions are first collected and then subject to individual, aliquot-by-aliquot analyses. The real-time LC-2D NMR experiment hereby introduced can be implemented in a straightforward manner using modern commercial LC-NMR hardware, thus opening up immediate possibilities in high-throughput characterizations of complex molecules. We have recently proposed and demonstrated an approach that enables the acquisition of multidimensional nuclear magnetic resonance (NMR) spectra within a single scan. A promising application opened up by this new accelerated form of data acquisition concerns the possibility of monitoring in real time the chemical nature of analytes subject to a continuous flow. The present paper illustrates such potential, with the real-time acquisition of a series of 2D 1H NMR spectra arising from a mixture of compounds subject to a continuous liquid chromatography (LC) separation. This real-time 2D NMR identification of chemicals eluted minutes apart under usual LC−NMR conditions differs from the way in which LC−2D NMR has hitherto been carried out, which relies on stopped-flow modes of operations whereby fractions are first collected and then subject to individual, aliquot-by-aliquot analyses. The real-time LC−2D NMR experiment hereby introduced can be implemented in a straightforward manner using modern commercial LC−NMR hardware, thus opening up immediate possibilities in high-throughput characterizations of complex molecules. We have recently proposed and demonstrated an approach that enables the acquisition of multidimensional nuclear magnetic resonance (NMR) spectra within a single scan. A promising application opened up by this new accelerated form of data acquisition concerns the possibility of monitoring in real time the chemical nature of analytes subject to a continuous flow. The present paper illustrates such potential, with the real-time acquisition of a series of 2D 1H NMR spectra arising from a mixture of compounds subject to a continuous liquid chromatography (LC) separation. This real-time 2D NMR identification of chemicals eluted minutes apart under usual LC-NMR conditions differs from the way in which LC-2D NMR has hitherto been carried out, which relies on stopped-flow modes of operations whereby fractions are first collected and then subject to individual, aliquot-by-aliquot analyses. The real-time LC-2D NMR experiment hereby introduced can be implemented in a straightforward manner using modern commercial LC-NMR hardware, thus opening up immediate possibilities in high-throughput characterizations of complex molecules. |
Author | Aronzon, Dina Karton, Amir Frydman, Lucio Shapira, Boaz |
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Cites_doi | 10.1021/ac026203i 10.1021/ja0350785 10.1021/ja030055b 10.1016/S1090-7807(03)00177-0 10.1002/0470854820 10.1006/jmra.1996.0059 10.1073/pnas.252644399 10.1016/S0378-4347(00)00479-5 |
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References | Albert K. (ja0389422b00002/ja0389422b00002_1) 2002 Barjat H. (ja0389422b00006/ja0389422b00006_1) 1996; 119 Shrot Y. (ja0389422b00010/ja0389422b00010_1) 2003; 125 Ernst R. R. (ja0389422b00003/ja0389422b00003_1) 1987 Frydman L. (ja0389422b00004/ja0389422b00004_1) 2002; 99 Braunschweiler L. (ja0389422b00007/ja0389422b00007_1) 1983; 53 Spraul M. (ja0389422b00009/ja0389422b00009_1) 2003; 75 Wilson I. D. (ja0389422b00001/ja0389422b00001_1) 2000; 748 Frydman L. (ja0389422b00005/ja0389422b00005_1) 2003; 125 Shrot Y. (ja0389422b00008/ja0389422b00008_1) 2003; 164 |
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Title | Real-Time 2D NMR Identification of Analytes Undergoing Continuous Chromatographic Separation |
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