## Abstract Crystallization of metastable α and stable γ polymorphs of glycine was carried out from aqueous solution in the presence of ammonia. Pure aqueous solution and solution with lower concentration of ammonia yield α nucleation and solution with a critical concentration of ammonia yield γ nu
Comment to 13C-NMR studies of α and γ polymorphs of glycine
✍ Scribed by M.J. Potrzebowski; P. Tekely; Y. Dusausoy
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 149 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0926-2040
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✦ Synopsis
Glycine provided to research laboratories by chemical companies can contain different polymorphs and/or mixture of polymorphs. The alpha- and gamma-glycine differ slightly in 13C shielding parameters and very much in dynamic properties. The isotropic values of chemical shifts for carboxyl groups of alpha- and gamma-glycine are found to be delta(iso) = 176.50 ppm and delta(iso) = 174.60 ppm, respectively. By using cross-polarization contact time equal to 20 ms, the intensity of carboxyl signal arising from gamma-glycine is reduced almost to zero, while that of alpha-glycine is only slightly depleted compared to the intensity of signal recorded at contact time of 1 ms. In contrast, for alpha-form, the 13C T1 relaxation time of carboxyl carbon is five times shorter compared to gamma-form.
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