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Infrared spectroscopic confirmation of [alpha]-lactone formation in the dissociation of a gaseous amino acid
The product obtained upon collision-induced dissociation of sulfonated phenylalanine in the gas phase has been investigated by using infrared multiphoton dissociation spectroscopy with a free-electron laser. This confirms that the product formed by loss of ammonia from the amino acid is the [alpha]-...
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Published in: | Journal of physical organic chemistry 2017-02, Vol.30 (2) |
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creator | Wenthold, Paul G Koirala, Damodar Somogyi, Arpad Poutsma, J C |
description | The product obtained upon collision-induced dissociation of sulfonated phenylalanine in the gas phase has been investigated by using infrared multiphoton dissociation spectroscopy with a free-electron laser. This confirms that the product formed by loss of ammonia from the amino acid is the [alpha]-lactone, as had been deduced previously based on qualitative analysis and electronic structure calculations. Spectroscopically, the structure is confirmed by the presence of the carbonyl stretching peak at 1915cm-1 and supported by excellent agreement between the predicted and observed S-O stretching bands. The agreement between predicted relative intensities is not as good, but can be attributed to the nonlinear process of IRMPD. Copyright © 2016 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/poc.3606 |
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This confirms that the product formed by loss of ammonia from the amino acid is the [alpha]-lactone, as had been deduced previously based on qualitative analysis and electronic structure calculations. Spectroscopically, the structure is confirmed by the presence of the carbonyl stretching peak at 1915cm-1 and supported by excellent agreement between the predicted and observed S-O stretching bands. The agreement between predicted relative intensities is not as good, but can be attributed to the nonlinear process of IRMPD. 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This confirms that the product formed by loss of ammonia from the amino acid is the [alpha]-lactone, as had been deduced previously based on qualitative analysis and electronic structure calculations. Spectroscopically, the structure is confirmed by the presence of the carbonyl stretching peak at 1915cm-1 and supported by excellent agreement between the predicted and observed S-O stretching bands. The agreement between predicted relative intensities is not as good, but can be attributed to the nonlinear process of IRMPD. 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This confirms that the product formed by loss of ammonia from the amino acid is the [alpha]-lactone, as had been deduced previously based on qualitative analysis and electronic structure calculations. Spectroscopically, the structure is confirmed by the presence of the carbonyl stretching peak at 1915cm-1 and supported by excellent agreement between the predicted and observed S-O stretching bands. The agreement between predicted relative intensities is not as good, but can be attributed to the nonlinear process of IRMPD. Copyright © 2016 John Wiley & Sons, Ltd.</abstract><cop>Bognor Regis</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/poc.3606</doi></addata></record> |
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title | Infrared spectroscopic confirmation of [alpha]-lactone formation in the dissociation of a gaseous amino acid |
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