Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10254
Title: Crystallographic evidence of Gly-d,l-Met oxidation to its sulfoxide in the presence of gold(III): Solid solution of the racemic mixture of two diastereo-isomers
Authors: Rychlewska, Urszula
Warżajtis, Beata
Glišić, Biljana
Rajković, Snežana
Djuran, Miloš
Journal: Acta Crystallographica Section C: Crystal Structure Communications
Issue Date: 17-Feb-2010
Abstract: Crystallographic analysis of a solid solution of two diastereoisomers, i.e. ({(1S,R)-1-carb-oxy-3-[(R,S)-methyl-sul-fin-yl]propyl}amino-carbonyl) methanaminium tetra-chlorido-aur-ate(III) and ({(1S,R)-1-carb-oxy-3-[(S,R)- methyl-sulfinyl]propyl}amino-carbonyl)methanaminium tetra-chloridoaurate(III), (C7H15N2O4S)[AuCl4], has shown that in the presence of gold(III), the methio-nine part of the Gly-d,l-Met dipeptide is oxidized to sulfoxide, and no coordination to the AuIII cation through the S atom of the sulfoxide is observed. In view of our observation, literature reports that methio-nine acts as an N,S-bidentate donor ligand forming stable gold(III) complexes require verification. Moreover, it has been demonstrated that crystallization of the oxidation product leads to a substantial 77:23 excess of both S-methio-nine/R-sulfoxide and R-methio-nine/S-sulfoxide over S-methio-nine/S-sulfoxide and R-methio-nine/R-sulfoxide. The presence of two different di-astereoisomers at the same crystallographic site is a source of static disorder at this site. © 2010 International Union of Crystallography.
URI: https://scidar.kg.ac.rs/handle/123456789/10254
Type: journal article
DOI: 10.1107/S0108270110001666
ISSN: 01082701
SCOPUS: 76449115679
Appears in Collections:Faculty of Science, Kragujevac

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