A new synthetic strategy for the preparation of persistent paramagnetic cyclodextrin-based rotaxanes is described. The method consists in the formation of inclusion complexes between a-cyclodextrin (a-CD) and a,x-dithiols containing an octamethylene chain covalently trapped by bulky stoppers composed of 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) radical fragments. Interaction of a-CD (the bead) and 1,8-octanedithiol (the thread) occurs in aqueous alkaline media and encapsulation is obtained by nucleophilic substitution at both termini of the linear component with a bulky paramagnetic iodide [2,2,6,6-tetramethyl-4-(2-iodoacetamide)piperidine-N-oxyl]. Structure determination of the new [2]rotaxane by 1H NMR is reported and the spectroscopic data are discussed.
E. Mezzina, P. Franchi, M. Lucarini (2007). Synthesis and characterization of a persistent paramagnetic rotaxane based on afa-cyclodextrin and alfa,gamma-alkyl disulfides. JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, 57, 179-183 [10.1007/s10847-006-9197-8].
Synthesis and characterization of a persistent paramagnetic rotaxane based on afa-cyclodextrin and alfa,gamma-alkyl disulfides
MEZZINA, ELISABETTA;FRANCHI, PAOLA;LUCARINI, MARCO
2007
Abstract
A new synthetic strategy for the preparation of persistent paramagnetic cyclodextrin-based rotaxanes is described. The method consists in the formation of inclusion complexes between a-cyclodextrin (a-CD) and a,x-dithiols containing an octamethylene chain covalently trapped by bulky stoppers composed of 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) radical fragments. Interaction of a-CD (the bead) and 1,8-octanedithiol (the thread) occurs in aqueous alkaline media and encapsulation is obtained by nucleophilic substitution at both termini of the linear component with a bulky paramagnetic iodide [2,2,6,6-tetramethyl-4-(2-iodoacetamide)piperidine-N-oxyl]. Structure determination of the new [2]rotaxane by 1H NMR is reported and the spectroscopic data are discussed.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.