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   <subfield code="a">Synthesis and Structural Characterization of Three Phenylsulfonyl Derivatives: Influence of Halogen Substituents on the Intermolecular Interactions</subfield>
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   <subfield code="c">[C. Castera, M. Crozet, M. Giorgi, P. Vanelle]</subfield>
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   <subfield code="a">Synthesis and X-ray structural determination of three halogenated nitroimidazo[1,2-a]pyridine phenylsulfonyl derivatives are reported. (2) is monoclinic P21/c with a=9.6679(1), b=11.3642(2), c=15.2189(2)Å, β=105.9053(7)°; (3) is triclinic P −1 with a=8.5556(2), b=13.1191(3), c=15.5132(4)Å, α=76.0110(8), β=89.1768(8), γ=78.953(2)°; (4) is monoclinic P21/c with a=15.3353(2), b=8.8621(2), c=11.4189(3)Å, β=90.9704(7)°. In the title compounds that differ by the nature and number of halogen substituents, the arylsulfonyl moieties are oriented differently relatively to the nitroimidazopyridine. Moreover non-classical intermolecular interactions are revealed by the X-ray analysis. Graphical Abstract: The X-ray structures of three halogenated nitroimidazo[1,2-a]pyridine phenylsulfonyl derivatives reveal different intermolecular interactions within the crystals. C. Castera, M. D. Crozet, M. Giorgi and P. Vanelle The X-ray structures of three halogenated nitroimidazo[1,2-a]pyridine phenylsulfonyl derivatives reveal different intermolecular interactions within the crystals. Synthesis and structural characterization of three phenylsulfonyl derivatives: influence of halogen substituents on the intermolecular interactions. C. Castera,1 M. D. Crozet,1 M. Giorgi,2 and P. Vanelle1* 1Laboratoire de Chimie Organique Pharmaceutique, UMR CNRS 6517, Université de la Méditerranée, Faculté de Pharmacie, 27 Boulevard Jean Moulin, 13385 Marseille cedex 5, France ; 2Spectropôle-RX, Université Paul Cézanne Aix-Marseille III, Faculté des Sciences et Techniques, Avenue Escadrille Normandie-Niemen, 13397 Marseille cedex 20, France.</subfield>
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