Carboxylic acid–pyridine supramolecular heterocatemer in a co-crystal

Abstract

Robustness of carboxylic acid–pyridine supramolecular heterosynthon was examined in three 1:2 binary co-crystals of 4,4′-bipyridine with monocarboxylic acids, (4,4′-bipyridine)·( dl-hydroxyphenylacetic acid) 2, 1; (4,4′-bipyridine) 0.5·(4-bromonaphthalene-1-carboxylic acid), 2 and (4,4′-bipyridine) 0.5·(4-methylbenzoic acid), 3. All the three co-crystals form “two-component supermolecules” (consisting of one molecule of 4,4′-bipyridine and two molecules of the relevant carboxylic acid) stabilized through carboxylic acid–pyridine heterosynthons. Co-crystals 1 and 2 exhibits the expected carboxylic acid–pyridine dimer (heterodimer I) whereas co-crystal 3 forms a novel carboxylic acid–pyridine catemer (heterocatemer II).