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2-Amino-5-bromo­pyridinium hydrogen succinate

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      Abstract

      In the title compound, C5H6BrN2 +·C4H5O4 −, the pyridine N atom of the 2-amino-5-bromo­pyridine mol­ecule is protonated. The protonated N atom and the amino group are linked via N—H⋯O hydrogen bonds to the carboxyl­ate O atoms of the singly deprotonated succinate anion. The hydrogen succinate anions are linked via O—H⋯O hydrogen bonds. A weak inter­molecular C—H⋯O hydrogen bond is also observed.

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      Affiliations
      [a ]X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia
      Author notes
      Correspondence e-mail: hkfun@ 123456usm.my
      [‡]

      Thomson Reuters ResearcherID: A-3561-2009.

      Journal
      Acta Crystallogr Sect E Struct Rep Online
      Acta Cryst. E
      Acta Crystallographica Section E: Structure Reports Online
      International Union of Crystallography
      1600-5368
      01 March 2010
      27 February 2010
      27 February 2010
      : 66
      : Pt 3 ( publisher-idID: e100300 )
      : o689-o690
      2983627
      21580432
      is2526
      10.1107/S1600536810006495
      ACSEBH S1600536810006495
      © Hemamalini and Fun 2010

      This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

      Categories
      Organic Papers

      Materials characterization

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