Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/2630
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dc.contributor.authorFaleni, N-
dc.contributor.authorJacobs, Ayesha-
dc.contributor.authorTaljaard, Jana H.-
dc.date.accessioned2015-04-29T10:39:43Z-
dc.date.available2015-04-29T10:39:43Z-
dc.date.issued2009-
dc.identifier.citationFaleni, N., Jacobs, A., & Taljaard, J. H. (2009). Inclusion Compounds of the Host 9-(4-Methylphenyl)-9H-xanthen-9-ol with a Series of Organic Guests. Journal of Chemical Crystallography, 39(4): 285-292. [https://link.springer.com/article/10.1007/s10870-008-9475-y]en_US
dc.identifier.otherhttp://link.springer.com/article/10.1007/s10870-008-9475-y-
dc.identifier.urihttp://hdl.handle.net/11189/2630-
dc.identifier.urihttp://dx.doi.org/10.1007/s10870-008-9475-yen
dc.description.abstractThe host 9-(4-methylphenyl)-9H-xanthen-9-ol (H) forms inclusion compounds with the guests cyclohexane (H · ½CHEX), benzene (H · ½BENZ), 1,4-dioxane (H · ½DIOX), cyclohexanone (H · CYONE), N,N-dimethylformamide (H · DMF) and N,N-dimethylacetamide (H · DMA). For those guest molecules possessing electron acceptor atoms/functionalities hydrogen bonding with the host is the prominent mode of interaction and presents itself in the form of (Host)–OH···O(Guest) linkages. The cyclohexane and benzene guests however, occupy voids created by neighbouring host molecules which form hydrogen bonded dimers of the form (Host)–OH···O(Host). The structures of the inclusion compounds were investigated and their thermal stabilities determined. Selectivity experiments were also conducted.en_US
dc.language.isoenen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/en
dc.subjectInclusion compoundsen
dc.subjectKineticsen
dc.subjectSelectivityen
dc.titleInclusion compounds of the host 9-(4-methylphenyl)-9H-xanthen-9-ol with a series of organic guestsen_US
dc.type.patentArticleen_US
Appears in Collections:Appsc - Journal Articles (DHET subsidised)
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