In the title 1:1 adduct, C6H6N2O· C11H8O2, the amide group is slightly twisted out of the plane of the aromatic ring, with a C-C-C-N torsion angle of 25.11 (19)°, whereas the carboxylic acid group is approximately coplanar with the bicylic ring system, with a C-C-C-O torsion angle of 10.9 (2)°. The amide groups from two isonicotinamide molecules form a dimer via N-H⋯O hydrogen bonds. In addition, the 2-naphthanoic acid molecule is hydrogen bonded to the pyridine unit of an isonicotinamide molecule via an O-H⋯N hydrogen bond. This gives rise to a centrosymmetric four-molecule chain, which is cross-linked by further N-H⋯O hydrogen bonds from the amide group.
CITATION STYLE
Madeley, L. G., Levendis, D. C., & Lemmerer, A. (2011). Isonicotinamide-2-naphthoic acid (1/1). Acta Crystallographica Section E: Structure Reports Online, 67(12). https://doi.org/10.1107/S1600536811050057
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