Electrostatic and short-range interactions compete in directing the structure of p-tert-butylcalix[4]arene inclusion compounds of fluorinated benzenes

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DOIResolve DOI: http://doi.org/10.1039/b401269k
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TypeArticle
Journal titleChem. Commun.
Chemical Communications
Issue12
Pages13601361; # of pages: 2
Abstractp-tert-Butylcalix[4]arene guest-host compounds with fluorinated benzenes show several structural motifs, thus indicating that the guest-host structure can be tuned to produce either a form with included guests or a form where the host self-includes with the guests outside the cavity.
Publication date
AffiliationNational Research Council Canada; NRC Steacie Institute for Molecular Sciences
Peer reviewedNo
NPARC number12330053
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Record identifiercf32f3b6-1019-4aca-bd6f-f0bcff8b7e8e
Record created2009-09-10
Record modified2016-05-09
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