α-phenyl-N-tert-butylnitrone-type derivatives bound to β-cyclodextrins:: Syntheses, thermokinetics of self-inclusion and application to superoxide spin-trapping
α-phenyl-N-tert-butylnitrone-type derivatives bound to β-cyclodextrins:: Syntheses, thermokinetics of self-inclusion and application to superoxide spin-trapping
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DOI:
10.1002/chem.200700369
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发表时间:
2007-01-01
影响因子:
4.3
通讯作者:
Tordo, Paul
中科院分区:
文献类型:
--
作者:
Bardelang, David;Charles, Laurence;Tordo, Paul
alpha-Phenyl-N-tert-butylnitrone (PBN) derivatives bound to beta-cyclodextrin derivatives have been synthesized. Inclusion of the PBN group into the P-cyclodextrin moiety is host- and temperature- dependent. In the case of the nitrone linked to permethylated cyclodextrin (Me3CD-PBN), the thermokinetic parameters are in favour of a slow chemical exchange between a tight and a loose complex. In contrast, 2,6-di-O-Me-beta-cyclodextrin-grafted PBN (Me2CD-PBN) exists either in a fast exchange or as a strongly self-associated complex. The covalent cyclodextrin-PBN compounds have been used to trap carbon and oxygen-centred free radicals. The self-associated forms of the P-CD-spin-traps are compatible with effective spin-trapping, affording spin-adducts with enhanced EPR signal intensities relative to noncovalent CD-nitrone systems or the nitrone alone. This kind of cyclodextrin-bound nitrone is the first type of covalent supramolecular spin-trap and should open new possibilities for the study of biological free radicals in vivo.