Location of TEMPO derivatives in micelles: subtle effect of the probe orientation

被引:31
作者
Aliaga, Carolina [1 ,2 ]
Bravo-Moraga, Felipe [3 ]
Gonzalez-Nilo, Danilo [3 ]
Marquez, Sebastian [1 ]
Luehr, Susan [1 ]
Mena, Geraldine [1 ]
Caroli Rezende, Marcos [1 ]
机构
[1] Univ Santiago Chile, Fac Quim & Biol, Santiago, Chile
[2] CEDENNA, Ctr Desarrollo Nanociencia & Nanotecnol, Santiago, Chile
[3] Univ Andres Bello, Fac Ciencias Biol, Ctr Bioinformat & Integrat Biol, Santiago, Chile
关键词
Partition constants; 4-AcyloxyTEMPO; Reduced Triton X-100 micelle; EPR g-factor; Molecular dynamics simulation; PSEUDOPHASE MODEL INTERPRETATION; MOLECULAR-DYNAMICS; PYRENE DERIVATIVES; NITROXIDES; HYDROPHOBICITY; EFFICIENCIES; DEPENDENCE; PARTITION; RADICALS; TRIPLET;
D O I
10.1016/j.foodchem.2015.07.036
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Partition coefficients for six 4-substituted derivatives of the 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) derivatives in aqueous solutions of reduced Triton X-100 (RTX-100) were determined by measurements of the probe EPR g-factor and of the fluorescence quenching of pyrene by the radical in the micelle. The partition constant attained a maximum value and then decreased with increasing probe hydrophobicity. Simulation of the probes inside the micelle showed that this trend could be rationalized by a change in the orientation of the 4-substituted TEMPO derivatives with the increasing substituent. chain-length. The use of the EPR g-factor for the determination of partition constants of radicals in micellar systems was thus validated as a reliable and sensitive method, capable of describing the probe orientation in its microenvironment. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:395 / 401
页数:7
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