Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/7243
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dc.contributor.authorNassimbeni, Luigi R.en_US
dc.contributor.authorBáthori, Nikoletta Ben_US
dc.contributor.authorPatel, Leena Desireeen_US
dc.contributor.authorSu, Hongen_US
dc.contributor.authorWeber, Edwinen_US
dc.date.accessioned2020-05-05T07:34:48Z-
dc.date.available2020-05-05T07:34:48Z-
dc.date.issued2015-
dc.identifier.citationNassimbeni, LR., Bathori, NB., Patel, LD. et al. 2015. Separation of xylenes by enclathration. Chemical Communications, 51: 3627-3629. [http://10.1039/c4cc05329j]en_US
dc.identifier.issn1359-7345-
dc.identifier.otherwww.rsc.org/chemcomm-
dc.identifier.urihttp://hdl.handle.net/11189/7243-
dc.description.abstractThe isomers of xylene have been separated by enclathration using three host compounds: 9,9′-bianthryl (H1), 9,9′-spirobifluorene (H2) and trans-2,3-dibenzoylspiro[cyclopropane-1,9-fluorene] (H3). The structures of each host with a single xylene isomer have been elucidated and, for H1, the relative lattice energies of the clathrates with ortho- and para-xylene have been evaluated.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.ispartofChemical Communicationsen_US
dc.subjectisomersen_US
dc.subjectxyleneen_US
dc.subjectenclathrationen_US
dc.subject9,9′-bianthryl (H1)en_US
dc.subject9,9′-spirobifluorene (H2)en_US
dc.subjecttrans-2,3-dibenzoylspiro[cyclopropane-1,9-fluorene] (H3)en_US
dc.titleSeparation of xylenes by enclathrationen_US
dc.identifier.doihttp://10.1039/c4cc05329j-
dc.typeArticleen_US
Appears in Collections:Appsc - Journal Articles (not DHET subsidised)
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