Gabapentin-lactum–chloranilic acid (1/1)

Jasinski, Jerry P. and Butcher, Ray J. and Hakim Al-arique, Q. N. M. and Yathirajan, H. S. and Narayana, B. (2010) Gabapentin-lactum–chloranilic acid (1/1). Acta Crystallographica Section E, 66 (1). o163-o164. ISSN 2056-9890

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Official URL: https://doi.org/10.1107/S1600536809053410

Abstract

In the title compound, C9H15NO·C6H2Cl2O4 [sytematic name: 2-aza­spiro­[4.5]decan-3-one–chloranilic acid (1/1)], the cyclo­hexane ring of the lactam molecule adopts a slightly distorted normal chair conformation and the five-membered 3-aza­spiro ring is in a slightly distorted chair conformation. The dihedral angle between the least-squares planes of the cyclohexane and 3-azaspiro rings is 84.0 (3)°. In the crystal, the chloranilic acid mol­ecule and the gabapentin-lactum mol­ecules are held together by strong inter­molecular N—H⋯O and O—H⋯O hydrogen bonds with two bifurcated O acceptor atoms on the chloranilic acid mol­ecule and one on the gabapentin-lactum mol­ecule, each bonding with an inter- and intra­molecular hydrogen bond. The molecules are linked into chains parallel to (011) and propagating along the b axis.

Item Type: Article
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: MUL SWAPNA user
Date Deposited: 06 Nov 2019 09:38
Last Modified: 06 Nov 2019 09:38
URI: http://eprints.uni-mysore.ac.in/id/eprint/9847

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