Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/2707
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dc.contributor.authorRamon, Gaëlle-
dc.contributor.authorJacobs, Ayesha-
dc.contributor.authorMasuku, Lungile ZN-
dc.contributor.authorNassimbeni, Luigi R.-
dc.date.accessioned2015-05-16T06:23:29Z-
dc.date.available2015-05-16T06:23:29Z-
dc.date.issued2009-
dc.identifier.citationRamon, G., Jacobs, A., Masuku, L. Z., & Nassimbeni, L. R. (2009). Selectivity by benzopinacol. CrystEngComm, 11(11): 2332-2337. [https://doi.org/10.1039/B905248H]en_US
dc.identifier.issn1466-8033-
dc.identifier.otherDOI is 10.1039/B905248H-
dc.identifier.urihttp://dx.doi.org/10.1039/B905248H-
dc.identifier.urihttp://hdl.handle.net/11189/2707-
dc.description.abstractThe host molecule 1,1,2,2-tetraphenylethane-1,2-diol forms inclusion compounds with THF, DMA and DMF with a constant host[thin space (1/6-em)]:[thin space (1/6-em)]guest ratio of 1[thin space (1/6-em)]:[thin space (1/6-em)]2. The structures of these three inclusion compounds were solved as well as the structure of a mixed guest compound. We studied the selectivity of the host towards all three guests and determined the activation energy of guest desorption for the DMA and DMF compounds.en_US
dc.language.isoenen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/en
dc.titleSelectivity by benzopinacolen_US
dc.type.patentArticleen_US
Appears in Collections:Appsc - Journal Articles (DHET subsidised)
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