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首页> 外文期刊>The Journal of Chemical Physics >Effect of micellar environment on Marcus correlation curves for photoinduced bimolecular electron transfer reactions - art. no. 034705
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Effect of micellar environment on Marcus correlation curves for photoinduced bimolecular electron transfer reactions - art. no. 034705

机译:胶束环境对光诱导双分子电子转移反应的Marcus相关曲线的影响-艺术。没有。 034705

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摘要

Photoinduced electron transfer (ET) between coumarin dyes and aromatic amine has been investigated in two cationic micelles, namely, cetyltrimethyl ammonium bromide (CTAB) and dodecyltrimethyl ammonium bromide (DTAB), and the results have been compared with those observed earlier in sodium dodecyl sulphate (SDS) and triton-X-100 (TX-100) micelles for similar donor-acceptor pairs. Due to a reasonably high effective concentration of the amines in the micellar Stern layer, the steady-state fluorescence results show significant static quenching. In the time-resolved (TR) measurements with subnanosecond time resolution, contribution from static quenching is avoided. Correlations of the dynamic quenching constants (k(q)(TR)), as estimated from the TR measurements, show the typical bell-shaped curves with the free-energy changes (Delta G(0)) of the ET reactions, as predicted by the Marcus outersphere ET theory. Comparing present results with those obtained earlier for similar coumarin-amine systems in SDS and TX-100 micelles, it is seen that the inversion in the present micelles occurs at an exergonicity (-Delta G(0)>similar to 1.2-1.3 eV) much higher than that observed in SDS and TX-100 micelles (-Delta G(0 >)similar to 0.7 eV), which has been rationalized based on the relative propensities of the ET and solvation rates in different micelles. In CTAB and DTAB micelles, the k(q)(TR) values are lower than the solvation rates, which result in the full contribution of the solvent reorganization energy (lambda(s)) towards the activation barrier for the ET reaction. Contrary to this, in SDS and TX-100 micelles, k(q)(TR) values are either higher or comparable with the solvation rates, causing only a partial contribution of lambda(s) in these cases. Thus, Marcus inversion in present cationic micelles is inferred to be the true inversion, whereas that in the anionic SDS and neutral TX-100 micelles are understood to be the apparent inversion, as envisaged from two-dimensional ET theory. (c) 2005 American Institute of Physics.
机译:在两个阳离子胶束中研究了香豆素染料与芳香胺之间的光诱导电子转移(ET),即十六烷基三甲基溴化铵(CTAB)和十二烷基三甲基溴化铵(DTAB),并将该结果与之前在十二烷基硫酸钠中观察到的结果进行了比较。 (SDS)和triton-X-100(TX-100)胶束,用于相似的供体-受体对。由于胶束斯特恩层中胺的有效浓度相当高,因此稳态荧光结果显示出明显的静态猝灭。在亚纳秒时间分辨率的时间分辨(TR)测量中,避免了静态猝灭的影响。根据TR测量值估算的动态猝灭常数(k(q)(TR))的相关性显示了典型的钟形曲线以及ET反应的自由能变化(Delta G(0))由Marcus外圈ET理论得出。将当前结果与之前在SDS和TX-100胶束中类似香豆素-胺系统获得的结果进行比较,可以看出,当前胶束的倒置发生在能主性上(-Delta G(0)>类似于1.2-1.3 eV)远高于在SDS和TX-100胶束中观察到的值(-Delta G(0>)类似于0.7 eV),这已根据不同胶束中ET的相对倾向和溶剂化率进行了合理化。在CTAB和DTAB胶束中,k(q)(TR)值低于溶剂化率,这导致溶剂重组能(λ)完全对ET反应的活化势垒起作用。与此相反,在SDS和TX-100胶束中,k(q)(TR)值更高或与溶剂化率相当,在这些情况下仅导致部分λ的贡献。因此,根据二维ET理论的设想,目前阳离子胶束中的马库斯反演被认为是真正的反演,而阴离子SDS和中性TX-100胶束中的马库斯反演被认为是表面反演。 (c)2005年美国物理研究所。

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