Crystal engineering with hydrogen bonds and halogen bonds

dc.contributor.author Saha, Binoy K.
dc.contributor.author Nangia, Ashwini
dc.contributor.author Jaskólski, Mariusz
dc.date.accessioned 2022-03-27T09:30:57Z
dc.date.available 2022-03-27T09:30:57Z
dc.date.issued 2005-05-23
dc.description.abstract Molecular tapes mediated via strong O-H⋯N hydrogen bonds and weak C-I⋯O interactions are present in complexes of 4-nitrobenzoic acid·4-iodopyridine and 3,5-dinitrobenzoic acid·4-iodopyridine. Crystal structure of 4-nitrobenzamide·4-iodobenzamide has amide dimer tape and iodo⋯nitro interaction in orthogonal directions. There is good structural insulation in the hydrogen bonding and halogen bonding domains in these crystal structures. However, the less polarizable bromine and chlorine atoms show cross-pairing interactions that are less predictable. These preliminary results show that both carboxylic acid⋯pyridine and iodo⋯nitro heterosynthons may be simultaneously exploited for crystal design. © The Royal Society of Chemistry 2005.
dc.identifier.citation CrystEngComm. v.7
dc.identifier.issn 14668033
dc.identifier.uri 10.1039/b501693b
dc.identifier.uri http://xlink.rsc.org/?DOI=b501693b
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12999
dc.title Crystal engineering with hydrogen bonds and halogen bonds
dc.type Journal. Article
dspace.entity.type
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