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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Clark, C. G. | en |
| dc.contributor.author | Floudas, G. A. | en |
| dc.contributor.author | Lee, Y. J. | en |
| dc.contributor.author | Graf, R. | en |
| dc.contributor.author | Spiess, H. W. | en |
| dc.contributor.author | Mullen, K. | en |
| dc.date.accessioned | 2015-11-24T18:40:25Z | - |
| dc.date.available | 2015-11-24T18:40:25Z | - |
| dc.identifier.issn | 0002-7863 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/17615 | - |
| dc.rights | Default Licence | - |
| dc.subject | semifluorinated normal-alkanes | en |
| dc.subject | fluorous phase affinity | en |
| dc.subject | solid-state | en |
| dc.subject | nmr-spectroscopy | en |
| dc.subject | complexes | en |
| dc.subject | silver(i) | en |
| dc.subject | exchange | en |
| dc.subject | ethers | en |
| dc.subject | ions | en |
| dc.subject | hexaarylbenzenes | en |
| dc.title | Molecularly Tethered Amphiphiles as 3-D Supramolecular Assembly Platforms: Unlocking a Trapped Conformation | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.primary | Doi 10.1021/Ja900999f | - |
| heal.identifier.secondary | <Go to ISI>://000267630000050 | - |
| heal.identifier.secondary | http://pubs.acs.org/doi/pdfplus/10.1021/ja900999f | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιών | el |
| heal.publicationDate | 2009 | - |
| heal.abstract | A 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.journalName | J Am Chem Soc | en |
| heal.journalType | peer reviewed | - |
| heal.fullTextAvailability | TRUE | - |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Clark-2009-Molecularly Tethered.pdf | 678.06 kB | Adobe PDF | View/Open Request a copy |
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