Hydrogen-bonded supramolecular motifs in 4,4'-bipyridinium 8-hydroxy-7-iodoquinoline-5-sulfonate dihydrate
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Updated: Aug 24, 2026

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
Madhukar Hemamalini1, Packianathan Thomas Muthiah, Gabriele Bocelli
1Department of Chemistry, Bharathidasan University, Tiruchirappalli 620 024, Tamil Nadu, India.
Abstract:
In the title compound, C(10)H(9)N(2)(+).C(9)H(5)INO(4)S(-).2H(2)O, the 4,4'-bipyridine molecule is protonated at one of the pyridine N atoms. These moieties self-assemble into a supramolecular chain along the a axis through N-H.N hydrogen bonds. The quinolinol OH group acts as a donor with respect to a sulfonate O atom [O-H.O(sulfonate)] and acts as an acceptor with respect to a C-H group of ferron [C-H.O(hydroxy)], forming a supramolecular chain along the b axis. These two types of supramolecular chains (one type made up of bipyridine motifs and the other made up of sulfoxine motifs) interact via pi-pi stacking, generating a three-dimensional framework. These chains are further crosslinked by C-H.O hydrogen bonds and O-H.O hydrogen bonds involving water molecules.
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