Polymorphism and Modulation of Para-Substituted l -Phenylalanine
Author(s) -
Leyla-Cann Söğütoğlu,
Martin Lutz,
Hugo Meekes,
R. De Gelder,
Elias Vlieg
Publication year - 2017
Publication title -
crystal growth and design
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.966
H-Index - 155
eISSN - 1528-7505
pISSN - 1528-7483
DOI - 10.1021/acs.cgd.7b00747
Subject(s) - substituent , chemistry , phenylalanine , molecule , crystal structure , stereochemistry , fluorine , crystallography , superstructure , polymorphism (computer science) , ring (chemistry) , methyl group , modulation (music) , polar , group (periodic table) , amino acid , physics , organic chemistry , biochemistry , astronomy , gene , genotype , acoustics , thermodynamics
The crystal structure of para -methyl-l-phenylalanine at 230 K resembles that of the para-fluorinated analogue from the literature but is commensurately modulated with seven molecules in the asymmetric unit ( Z ' = 7). At 100 K, the superstructure loses its modulation, leading to a unit cell with Z ' = 1, with clear disorder in the phenyl ring orientations. The methyl-substituent in para -methyl-l-phenylalanine has, in contrast to fluorine, no polar interactions with protons of neighboring molecules, which might allow for the well-defined modulation of the crystal structure at 230 K.
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