Water-mediated multicenter synthon and aromatic C-H → N isostructurality
Water-mediated multicenter synthon and aromatic C-H → N isostructurality
| dc.contributor.author | Babu, N. Jagadeesh | |
| dc.contributor.author | Nangia, Ashwini | |
| dc.date.accessioned | 2022-03-27T09:29:52Z | |
| dc.date.available | 2022-03-27T09:29:52Z | |
| dc.date.issued | 2006-08-01 | |
| dc.description.abstract | A strong, cooperative ⋯O hydrogen bond network directs isostructurality in pyrazine tetracarboxylic acid, pyridine tetracarboxylic acid, and pyromellitic acid dihydrates. H2O and COOH groups reorganize their H bonding groups in an invariant network leading to O w-H⋯N → C-H⋯OW mimicry. The degree of similarity is related to the size of the multicenter synthon and the strength of the Oacid-H⋯OWater hydrogen bond. © 2006 American Chemical Society. | |
| dc.identifier.citation | Crystal Growth and Design. v.6(8) | |
| dc.identifier.issn | 15287483 | |
| dc.identifier.uri | 10.1021/cg060378u | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/cg060378u | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12978 | |
| dc.title | Water-mediated multicenter synthon and aromatic C-H → N isostructurality | |
| dc.type | Journal. Article | |
| dspace.entity.type |
Files
License bundle
1 - 1 of 1