Isonicotinamide–2-naphthoic acid (1/1)
Lee G. Madeley, Demetrius C. Levendis, Andreas Lemmerer
Acta Crystallographica Section E · 2011
doi:10.1107/s1600536811050057 (opens in a new tab)
We email you when a new notice or a question about this paper appears.
Abstract
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.
Abstract licence: CC BY
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.