Article Sidebar
Published:
Sep 18, 2015Keywords:
Article Details
Copyright for articles published in this journal is retained by the journal.
SAJChem applies the Creative Commons Attribution (CC BY) license to manuscripts we publish. This license was developed to facilitate open access – namely, free immediate access to, and unrestricted reuse of, original works of all types. Under this license, authors agree to make articles legally available for reuse, without permission or fees, for virtually any purpose. Anyone may copy, distribute or reuse these articles, as long as the author and original source are properly cited.
Main Article Content
Reaction of Hydrazine Hydrate with Oxalic Acid: Synthesis and Crystal Structure of Dihydrazinium Oxalate
Abstract
The reaction of oxalic acid with hydrazine hydrate (in appropriate mole ratio) forms the dihydrazinium oxalate under specific experimental condition. The title compound is a molecular salt containing two discrete hydrazinium cations and an oxalate anion. The oxalate anion is perfectly planar and there is a crystallographic centre of symmetry in the middle of the C-C bond. The C-O bond distances are almost equal indicating the presence of resonance in the oxalate ion. The crystal packing is stabilized by intermolecular N-H…Oand N-H…Nhydrogen bonds. The oxalate ions are linked together end to end through hydrogen bonds (via N2H5+ ions) and run parallel to the [101] direction. It is interesting to note that each oxalate group in the structure is surrounded by six hydrazinium ions through hydrogen bonding. Similarly, each hydrazinium ion is surrounded by three oxalate and one hydrazinium ion.
KEY WORDS: Hydrazine, oxalic acid, dihydrazinium oxalate, crystal structure.
