| Literature DB >> 25336255 |
Franziska Stefanie Ihlefeldt1, Fredrik Bjarte Pettersen, Aidan von Bonin, Malgorzata Zawadzka, Carl Henrik Görbitz.
Abstract
The solid-state structure of the amino acid phenylalanine (Phe) offers a potential key to understanding the behavior of a large class of important aromatic compounds. Obtaining good single crystals is, however, notoriously difficult. The structure of the common polymorph of Phe, form I, was first reported by Weissbuch et al. (as D-Phe) in 1990, but the correctness of the published C2 unit cell with two disordered molecules in the asymmetric unit was later questioned and other space groups suggested. The identity of form I of L-Phe is here established to be P21 with Z'=4, based on data from a well-diffracting single crystal grown from an acetic acid solution of the amino acid. A second new polymorph, form IV, together with the two recently described forms II and III provide unprecedented information on the structural complexity of this essential amino acid. It is furthermore documented that the racemate, dl-Phe, does not grow proper single crystals.Entities:
Keywords: amino acids; hydrogen bonds; polymorphism; pseudosymmetry; racemic twins
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Year: 2014 PMID: 25336255 DOI: 10.1002/anie.201406886
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336