Abstract
Formation of inclusion complexes between several cyclodextrin derivatives and TEMPO and DOXYL-based spin probes was studied by EPR spectroscopy. Competition between alkyl chains and nitroxide functionalities for cyclodextrin cavities leads to different types of complexation. Long alkyl chains in amphiphilic spin probes interact preferentially with cyclodextrins, and TEMPO units in such molecules are unaffected by complexation. DOXYL-type spin probes however form stronger complexes with cyclodextrins; this complexation changes hyper. ne splitting and tumbling rate of the nitroxide group. Comparison of EPR spectra of free cyclodextrin and cyclodextrin-based polymeric nanocapsules made it possible to assess the tumbling of the spin probe inside the cyclodextrin units without the contribution of the tumbling of the whole complex.
Original language | English |
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Pages (from-to) | 598-602 |
Number of pages | 5 |
Journal | Organic and Biomolecular Chemistry |
Volume | 7 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2009 |
Keywords
- BETA-CYCLODEXTRIN
- LABELED CYCLODEXTRINS
- AMPHIPHILIC CYCLODEXTRINS
- BIMODAL INCLUSION
- RESONANCE
- RADICALS
- WATER
- SUPEROXIDE
- MODEL