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IRMPD spectroscopy shows that AGG forms an oxazolone b2+ ion.


ABSTRACT: Infrared multiple photon dissociation (IRMPD) spectroscopy combined with theoretical vibrational spectra provides a powerful tool for probing structure. This technique has been used to probe the structure of protonated cyclic AG and the b(2)(+) ion from AGG. The experimental spectrum for protonated cyclo AG compares very well with the theoretical spectra for a diketopiperazine. The spectrum corresponds best to a combination of two structures protonation at the alanine and glycine amide oxygens. The experimental spectrum for the b(2)(+) ion from protonated AGG matches best to the theoretical spectrum for an oxazolone structure protonated on the ring nitrogen. In particular, the carbonyl stretching band at 1970 cm(-1) is blue-shifted by approximately 200 cm(-1) compared to the experimental spectrum for protonated cAG, indicating that these two structures are distinct. This is the first time that an IRPD spectrum of a b(2)(+) ion has been obtained and, for this ion, the oxazolone structure proposed based on prior calculations and experiments is confirmed by the spectroscopic method.

SUBMITTER: Yoon SH 

PROVIDER: S-EPMC2654176 | biostudies-other | 2008 Dec

REPOSITORIES: biostudies-other

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IRMPD spectroscopy shows that AGG forms an oxazolone b2+ ion.

Yoon Sung Hwan SH   Chamot-Rooke Julia J   Perkins Brittany R BR   Hilderbrand Amy E AE   Poutsma John C JC   Wysocki Vicki H VH  

Journal of the American Chemical Society 20081201 52


Infrared multiple photon dissociation (IRMPD) spectroscopy combined with theoretical vibrational spectra provides a powerful tool for probing structure. This technique has been used to probe the structure of protonated cyclic AG and the b(2)(+) ion from AGG. The experimental spectrum for protonated cyclo AG compares very well with the theoretical spectra for a diketopiperazine. The spectrum corresponds best to a combination of two structures protonation at the alanine and glycine amide oxygens.  ...[more]

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