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Saouane, Sofiane
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Saouane, Sofiane
Official Name
Saouane, Sofiane
Alternative Name
Saouane, S.
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2013Journal Article [["dc.bibliographiccitation.firstpage","1238"],["dc.bibliographiccitation.journal","ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS"],["dc.bibliographiccitation.lastpage","+"],["dc.bibliographiccitation.volume","69"],["dc.contributor.author","Saouane, Sofiane"],["dc.contributor.author","Buth, Gernot"],["dc.contributor.author","Fabbiani, Francesca P. A."],["dc.date.accessioned","2018-11-07T09:18:04Z"],["dc.date.available","2018-11-07T09:18:04Z"],["dc.date.issued","2013"],["dc.description.abstract","The X-ray single-crystal structure of (2S,5R,6R)-6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, commonly known as (+)-6-aminopenicillanic acid (C8H12N2O3S) and a precursor of a variety of semi-synthetic penicillins, has been determined from synchrotron data at 150K. The structure represents an ordered zwitterion and the crystals are nonmerohedrally twinned. The crystal structure is composed of a three-dimensional network built by three charge-assisted hydrogen bonds between the ammonium and carboxylate groups. The complementary analysis of the crystal packing by the PIXEL method brings to light the nature and ranking of the energetically most stabilizing intermolecular interaction energies. In accordance with the zwitterionic nature of the structure, PIXEL lattice energy calculations confirm the predominance of the Coulombic term (-379.1kJmol-1) ahead of the polarization (-141.4kJmol-1), dispersion (-133.7kJmol-1) and repulsion (266.3kJmol-1) contributions."],["dc.identifier.doi","10.1107/S0108270113025924"],["dc.identifier.isi","000326651300009"],["dc.identifier.pmid","24192166"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28321"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell"],["dc.relation.issn","1600-5759"],["dc.relation.issn","0108-2701"],["dc.title","Crystal structure and packing energy calculations of (+)-6-aminopenicillanic acid"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS
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