Molecularly Tethered Amphiphiles as 3-D Supramolecular Assembly Platforms: Unlocking a Trapped Conformation

dc.contributor.authorClark, C. G.en
dc.contributor.authorFloudas, G. A.en
dc.contributor.authorLee, Y. J.en
dc.contributor.authorGraf, R.en
dc.contributor.authorSpiess, H. W.en
dc.contributor.authorMullen, K.en
dc.date.accessioned2015-11-24T18:40:25Z
dc.date.available2015-11-24T18:40:25Z
dc.identifier.issn0002-7863-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/17615
dc.rightsDefault Licence-
dc.subjectsemifluorinated normal-alkanesen
dc.subjectfluorous phase affinityen
dc.subjectsolid-stateen
dc.subjectnmr-spectroscopyen
dc.subjectcomplexesen
dc.subjectsilver(i)en
dc.subjectexchangeen
dc.subjectethersen
dc.subjectionsen
dc.subjecthexaarylbenzenesen
dc.titleMolecularly Tethered Amphiphiles as 3-D Supramolecular Assembly Platforms: Unlocking a Trapped Conformationen
heal.abstractA fluorous biphasic hexa(3,5-substituted-phenyl)benzene (HPB), analogous to semifluorinated alkanes, was synthesized such that precise chemical and orthogonally directed, supramolecular placement of amphiphilic side chains at their bulk density was achieved. The grafting or tethering of incommensurate hydrocarbon and fluorocarbon chains to the rotationally flexible HPB core inextricably links intermolecular phase separation with intramolecular conformational behavior and results in rich self-assembly. The self-assembled structure was studied with polarized optical microscopy, differential scanning calorimetry, X-ray scattering, and (19)F magic-angle spinning solid-state NMR and found to be kinetically trapped with mixed fluorocarbon and hydrocarbon side chains, despite packing into a lattice defined by the HPB scaffold. The addition of 1% of the parent biphasic diphenylacetylene unlocks the frustrated conformation in the HPB, resulting in the formation of a thermodynamically favorable bilayer structure.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1021/Ja900999f-
heal.identifier.secondary<Go to ISI>://000267630000050-
heal.identifier.secondaryhttp://pubs.acs.org/doi/pdfplus/10.1021/ja900999f-
heal.journalNameJ Am Chem Socen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2009-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιώνel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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