Sulfonamide-pyridine-N-oxide cocrystals
Sulfonamide-pyridine-N-oxide cocrystals
| dc.contributor.author | Rajesh Goud, N. | |
| dc.contributor.author | Jagadeesh Babu, N. | |
| dc.contributor.author | Nangia, Ashwini | |
| dc.date.accessioned | 2022-03-27T09:27:21Z | |
| dc.date.available | 2022-03-27T09:27:21Z | |
| dc.date.issued | 2011-05-04 | |
| dc.description.abstract | Hydrogen-bond motifs for the supramolecular synthesis of sulfonamide-pyridine-N-oxide complexes were derived from the analysis of cocrystal structures of aryl sulfonamides and pyridine-N-oxides. The sulfonamide NH donor persistently interacts with the N-oxide acceptor via a N-H ··· O hydrogen bond, though the exact geometry of the motif, such as discrete (D), infinite chain C(4), cyclic motifs R 42 (8) or R22 (4), varies from structure to structure. Surprisingly, the two-point R22 (8) cyclic motif of N-H···O and C- H···O hydrogen bonds, analogous to the heterosynthon in carboxamide-pyridine-N-oxide cocrystals, was not observed in sulfonamide-N-oxide cocrystals. The utility of this model study is demonstrated by making cocrystals of Furosemide with 4,4′-bipyridine-N,N′-dioxide and isonicotinamide-N-oxide. © 2011 American Chemical Society. | |
| dc.identifier.citation | Crystal Growth and Design. v.11(5) | |
| dc.identifier.issn | 15287483 | |
| dc.identifier.uri | 10.1021/cg200094x | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/cg200094x | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12926 | |
| dc.title | Sulfonamide-pyridine-N-oxide cocrystals | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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