García-Río L, Leis J R, Mejuto J C, Navarro-Vázquez A, Pérez-Juste J, Rodriguez-Dafonte P
Departamento de Química Física, Facultad de Químicia, Universidad de Santiago de Compostela, Santiago de Compostela, Spain.
Langmuir. 2004 Feb 3;20(3):606-13. doi: 10.1021/la035477d.
The basic hydrolysis of crystal violet (CV) in mixed systems consisting of beta-cyclodextrin (beta-CD) and a micelle-forming surfactant, cetyltrimethylammonium chloride (CTACl), has been studied. beta-CD was found to catalyze the basic hydrolysis of CV through the interaction of its hydroxyl group, in its deprotonated form, with the carbocation in the complexed substrate. The addition of small amounts of CTACl, with [CTACl] below the critical micelle concentration, to beta-CD solutions does not have an effect upon the observed rate constant for the basic hydrolysis of CV. This behavior is different from that observed for the alkaline hydrolysis of N-methyl-N-nitroso-p-toluenesulfonamide and nitrophenyl acetates in mixed beta-CD/cationic surfactant systems. The proposed mechanism allows us to explain the experimental results on the basis of the high percentage of uncomplexed beta-CD in equilibrium with the micellar system, the low CV concentration, and the high value for the binding constant of CV by beta-CD.
研究了结晶紫(CV)在由β-环糊精(β-CD)和形成胶束的表面活性剂十六烷基三甲基氯化铵(CTACl)组成的混合体系中的碱性水解。发现β-CD通过其去质子化形式的羟基与复合底物中的碳正离子相互作用来催化CV的碱性水解。向β-CD溶液中加入少量[CTACl]低于临界胶束浓度的CTACl,对观察到的CV碱性水解速率常数没有影响。这种行为与在混合β-CD/阳离子表面活性剂体系中N-甲基-N-亚硝基对甲苯磺酰胺和硝基苯基乙酸酯的碱性水解所观察到的行为不同。所提出的机理使我们能够基于与胶束体系平衡的未复合β-CD的高百分比、低CV浓度以及β-CD对CV的高结合常数来解释实验结果。