[5]Rotaxane and [5]pseudorotaxane based on cucurbit[6]uril and anchored to a meso-tetraphenyl porphyrin

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dc.citation.epage380en_US
dc.citation.issueNumber3-4en_US
dc.citation.spage373en_US
dc.citation.volumeNumber55en_US
dc.contributor.authorTuncel, D.en_US
dc.contributor.authorCindir, N.en_US
dc.contributor.authorKoldemir, Ü.en_US
dc.date.accessioned2016-02-08T10:18:35Z
dc.date.available2016-02-08T10:18:35Z
dc.date.issued2006en_US
dc.departmentDepartment of Chemistryen_US
dc.description.abstractWater soluble [5]rotaxane and [5]pseudorotaxane based on cucurbit[6]uril and anchored to a meso-tetraphenyl porphyrin have been synthesized and characterized by spectroscopic methods (1H-NMR, 13C-NMR and UV), and by elemental analysis, and mass spectrometry. The preliminary results of the pH-driven switching properties of [5]rotaxane investigated through 1H-NMR spectroscopy are reported. These results were compared with those obtained from a model porphyrin, which was prepared by the de-threading cucurbit[6]uril from [5]pseudorotaxane under basic conditions. © Springer 2006.en_US
dc.description.provenanceMade available in DSpace on 2016-02-08T10:18:35Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 70227 bytes, checksum: 26e812c6f5156f83f0e77b261a471b5a (MD5) Previous issue date: 2006en
dc.identifier.doi10.1007/s10847-006-9112-3en_US
dc.identifier.issn0923-0750
dc.identifier.urihttp://hdl.handle.net/11693/23750
dc.language.isoEnglishen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/s10847-006-9112-3en_US
dc.source.titleJournal of Inclusion Phenomena and Macrocyclic Chemistryen_US
dc.title[5]Rotaxane and [5]pseudorotaxane based on cucurbit[6]uril and anchored to a meso-tetraphenyl porphyrinen_US
dc.typeArticleen_US

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