[5]Rotaxane and [5]pseudorotaxane based on cucurbit[6]uril and anchored to a meso-tetraphenyl porphyrin
| dc.citation.epage | 380 | en_US |
| dc.citation.issueNumber | 3-4 | en_US |
| dc.citation.spage | 373 | en_US |
| dc.citation.volumeNumber | 55 | en_US |
| dc.contributor.author | Tuncel, D. | en_US |
| dc.contributor.author | Cindir, N. | en_US |
| dc.contributor.author | Koldemir, Ü. | en_US |
| dc.date.accessioned | 2016-02-08T10:18:35Z | |
| dc.date.available | 2016-02-08T10:18:35Z | |
| dc.date.issued | 2006 | en_US |
| dc.department | Department of Chemistry | en_US |
| dc.description.abstract | Water 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.identifier.doi | 10.1007/s10847-006-9112-3 | en_US |
| dc.identifier.issn | 0923-0750 | |
| dc.identifier.uri | http://hdl.handle.net/11693/23750 | |
| dc.language.iso | English | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1007/s10847-006-9112-3 | en_US |
| dc.source.title | Journal of Inclusion Phenomena and Macrocyclic Chemistry | en_US |
| dc.title | [5]Rotaxane and [5]pseudorotaxane based on cucurbit[6]uril and anchored to a meso-tetraphenyl porphyrin | en_US |
| dc.type | Article | en_US |
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