Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/7243
Title: Separation of xylenes by enclathration
Authors: Nassimbeni, Luigi R. 
Báthori, Nikoletta B 
Patel, Leena Desiree 
Su, Hong 
Weber, Edwin 
Keywords: isomers;xylene;enclathration;9,9′-bianthryl (H1);9,9′-spirobifluorene (H2);trans-2,3-dibenzoylspiro[cyclopropane-1,9-fluorene] (H3)
Issue Date: 2015
Publisher: Royal Society of Chemistry
Source: Nassimbeni, LR., Bathori, NB., Patel, LD. et al. 2015. Separation of xylenes by enclathration. Chemical Communications, 51: 3627-3629. [http://10.1039/c4cc05329j]
Journal: Chemical Communications 
Abstract: The 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.
URI: http://hdl.handle.net/11189/7243
ISSN: 1359-7345
DOI: http://10.1039/c4cc05329j
Appears in Collections:Appsc - Journal Articles (not DHET subsidised)

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