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维生素C对菲醌三重激发态的淬灭机理及动力学研究
引用本文:许新胜,史蕾,刘毅,季学韩,崔执凤.维生素C对菲醌三重激发态的淬灭机理及动力学研究[J].化学物理学报,2011,24(2):150-154.
作者姓名:许新胜  史蕾  刘毅  季学韩  崔执凤
作者单位:安徽师范大学原子与分子物理研究所,芜湖241000;安徽师范大学原子与分子物理研究所,芜湖241000;安徽师范大学原子与分子物理研究所,芜湖241000;安徽师范大学原子与分子物理研究所,芜湖241000;安徽师范大学原子与分子物理研究所,芜湖241000
摘    要:用时间分辨电子自旋共振技术研究了乙二醇(EG)均相溶液和反胶束溶液中抗氧化剂维生素C(VC)对菲醌(PAQ)分子激发三重态3PAQ*的淬灭反应.利用反胶束模拟生物细胞和组织的生理环境.光解PAQ/EG-H2O均相溶液,3PAQ*与溶剂分子EG之间发生氢转移反应.当体系中加入VC后,3PAQ*不仅从EG上夺氢,还从VC上夺氢,VC对3PAQ*的淬灭速率常数为1.409×108 L/(mol·s), 反应受扩散控制. 在CTAB/EG-H2O和AOT/EG-H2O反胶束溶液中,3PAQ*和VC之间的夺氢反应发生在反胶束的水/油界面附近,3PAQ*扩散到油/水界面的过程降低了反应的速率.对于TX-100/EG-H2O反胶束溶液, 由于PAQ增溶于亲水的聚氧乙烯链中,VC对3PAQ*的淬灭速率常数比CTAB/EG-H2O和AOT/EG-H2O反胶束中的都大,甚至比EG-H2O均相溶液中的也略大.很强的VC负离子自由基As-的CIDEP信号来源于3PAQ*与VC之间发生抽氢反应过程中的三重态机理自旋极化转移

关 键 词:菲醌,维生素C,时间分辨电子自旋共振,反胶束
收稿时间:2010/12/4 0:00:00

TR-ESR Investigation on Reaction of Vitamin C with Excited Triplet of 9,10-phenanthrenequinone in Reversed Micelle Solutions
Xin-sheng Xu,Lei Shi,Yi Liu,Xue-han Ji and Zhi-feng Cui.TR-ESR Investigation on Reaction of Vitamin C with Excited Triplet of 9,10-phenanthrenequinone in Reversed Micelle Solutions[J].Chinese Journal of Chemical Physics,2011,24(2):150-154.
Authors:Xin-sheng Xu  Lei Shi  Yi Liu  Xue-han Ji and Zhi-feng Cui
Institution:Institute of Atomic and Molecular Physics, Anhui Normal University, Wuhu 241000, China;Institute of Atomic and Molecular Physics, Anhui Normal University, Wuhu 241000, China;Institute of Atomic and Molecular Physics, Anhui Normal University, Wuhu 241000, China;Institute of Atomic and Molecular Physics, Anhui Normal University, Wuhu 241000, China;Institute of Atomic and Molecular Physics, Anhui Normal University, Wuhu 241000, China
Abstract:Time-resolved electron spin resonance has been used to study quenching reactions between the antioxidant Vitamin C (VC) and the triplet excited states of 9,10-phenanthrenequinone (PAQ) in ethylene glycol-water (EG-H2O) homogeneous and inhomogeneous reversed micelle solutions. Reversed micelle solutions were used to be the models of physiological environment of biological cell and tissue. In PAQ/EG-H2O homogeneous solution, the excited triplet of PAQ (3PAQ*) abstracts hydrogen atom from solvent EG. In PAQ/VC/EG-H2O solution, 3PAQ* abstracts hydrogen atom not only from solvent EG but also from VC. The quenching rate constant of 3PAQ* by VC is close to the diffusion-controlled value of 1.41×108 L/(mol·s). In hexadecyltrimethylammonium bromide (CTAB)/EG-H2O and aerosol OT (AOT)/EG-H2O reversed micelle solutions, 3PAQ* and VC react around the water-oil interface of the reversed micelle. Exit of 3PAQ* from the lipid phase slows down the quenching reaction. For Triton X-100 (TX-100)/EG-H2O reversed micelle solution, PAQ and VC coexist inside the hydrophilic polyethylene glycol core, and the quenching rate constant of 3PAQ* by VC is larger than those in AOT/EG-H2O and CTAB/EG-H2O reversed micelle solutions, even a little larger than that in EG-H2O homogeneous solution. The strong emissive chemically in-duced dynamic electron polarization of As- resulted from the effective TM spin polarization transfer in hydrogen abstraction of 3PAQ* from VC.
Keywords:9  10-phenanthrenequinone  Vitamin C  Time-resolved electron spin resonance  Reversed micelle
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