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Micellar Effects on Intramolecular Charge Transfer Emission from Biphenylcarboxylic Acids

机译:胶束对联苯羧酸分子内电荷转移发射的影响

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摘要

The intramolecular charge transfer (ICT) phenomena of the photoexcited 2-biphenylcarboxylic acid (2BPCA) and 4-biphenylcarboxylic acid (4BPCA) have been investigated in some surfactant micellar solutions. The ICT emission of 4BPCA and 2BPCA in aqueous solution at sufficiently low pH (1-3) has been observed to be markedly quenched and blue-shifted upon addition of a cationic surfactant, cetyltrimethylammonium chloride (CTAC) in contrast to little change in anionic sodium dodecyl sulfate (SDS) and neutral Brij 35. An anionic emission band has been observed to be enhanced at expense of the ICT emission as a function of the concentration of CTAC. These results with the micellar effects on the fluorescence decay kinetics of 4BPCA suggest that formation of the ICT state of the excited acids is inhibited by CTAC-induced proton transfer as well as the decrease in the polarity and/or hydrogen-bonding ability of the micellar microenvironment entrapping the acids.
机译:在一些表面活性剂胶束溶液中,研究了光激发的2-联苯基羧酸(2BPCA)和4-联苯基羧酸(4BPCA)的分子内电荷转移(ICT)现象。已观察到,在添加足够低的pH值(1-3)的水溶液中,4BPCA和2BPCA的ICT排放显着淬灭并蓝移,而阴离子型钠的变化很小,而十六烷基三甲基氯化铵(CTAC)十二烷基硫酸盐(SDS)和中性Brij35。观察到阴离子发射带随着ICT发射的增加而增加,这是CTAC浓度的函数。胶束对4BPCA荧光衰减动力学的影响的这些结果表明,CTAC诱导的质子转移以及胶束的极性和/或氢键合能力的降低都抑制了激发酸的ICT状态的形成。包埋酸的微环境。

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