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ESR and ENDOR studies of dl-prolinexHCl single crystals

Journal Article · · J. Chem. Phys.; (United States)
OSTI ID:5574798

By means of ESR and ENDOR spectroscopy, single crystals of dl-prolinexHCl, Cl/sup -/H/sub 2/+N(CH/sub 2/)/sub 3/C/sub ..cap alpha../HCOOH, have been studied after x irradiation at 65 K and warming to 300 K. The ESR has been shown to be the result of two stable end products. One product, Cl/sup -/(CH/sub 2/)/sub 3/C/sub ..cap alpha../HCOOH, results from cleavage of the C/sub ..cap alpha../--N bond, a reaction common to all proline-related molecules studied to date. The C/sub ..cap alpha../--N cleavage reaction is analogous to the usual deamination reaction of other amino acids. The second product, not previously observed in proline-related molecules, has been identified as the result of abstraction of the hydrogen bound to C/sub ..cap alpha../. This product, Cl/sup -/H/sub 2/+N(CH/sub 2/)/sub 3/C/sub ..cap alpha../COOH, is characterized by four ..beta..-proton couplings. Evidently, the second product results in some manner from a primary cationic product of the proline molecule. Notable about the case of dl-prolinexHCl is that the concentration of the second product is equal to, or greater than, that of the more common product.

Research Organization:
Department of Physics and Astronomy, Georgia State University, Atlanta, Georgia 30303
OSTI ID:
5574798
Journal Information:
J. Chem. Phys.; (United States), Journal Name: J. Chem. Phys.; (United States) Vol. 83:5; ISSN JCPSA
Country of Publication:
United States
Language:
English