Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/4433
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dc.contributor.authorRamon, Gaëlle-
dc.contributor.authorJacobs, Ayesha-
dc.contributor.authorNassimbeni, Luigi R.-
dc.contributor.authorYav-Kabwit, Rodriguez-
dc.date.accessioned2016-06-23T06:26:30Z-
dc.date.available2016-06-23T06:26:30Z-
dc.date.issued2011-
dc.identifier.urihttp://dx.doi.org/10.1021/cg2004084-
dc.identifier.urihttp://hdl.handle.net/11189/4433-
dc.description.abstractInclusion compounds from p-tert-butylcalix[4] and [6]arenes were grown from chlorobenzene, bromobenzene, benzylamine, and ethylene diamine. The crystal structures of seven new compounds were elucidated, their host guest ratios were established, and their respective thermal stabilities were investigated. The kinetics of desorption of four of the compounds yielded their activation energies of decomposition. We established the selectivity profile of p-tert-butylcalix[4]arene for chlorobenzene versus bromobenzene as guests.en_US
dc.language.isoenen_US
dc.publisherCrystal Growth and Designen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/en
dc.subjectKineticsen_US
dc.subjectStructuresen_US
dc.subjectSelectivityen_US
dc.subjectp-tert-Butylcalixarenesen_US
dc.titleInclusion Compounds of p-tert-Butylcalixarenes: Structures, Kinetics, and Selectivityen_US
dc.type.patentArticleen_US
Appears in Collections:Appsc - Journal Articles (DHET subsidised)
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