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确定对氨基苯硫酚在银纳米粒子上选择性催化偶联反应生成的对,对'-二巯基偶氮苯。

Ascertaining p,p'-dimercaptoazobenzene produced from p-aminothiophenol by selective catalytic coupling reaction on silver nanoparticles.

机构信息

Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, P. O. Box 603-146, Beijing, 100190, People's Republic of China.

出版信息

Langmuir. 2010 Jun 1;26(11):7737-46. doi: 10.1021/la904479q.

Abstract

Combining experiment and theory, evidence from surface-enhanced Raman scattering (SERS) were obtained for p,p'-dimercaptoazobenzene (DMAB) produced from p-aminothiophenol (PATP) by selective catalytic coupling reaction on silver nanoparticles. The time-dependent SERS spectra of PATP are consistent with the calculated SERS spectra of DMAB, which is the direct evidence for the production of DMAB from PATP by selective catalytic coupling reaction on silver nanoparticles. The so-called "b(2) modes" of PATP is the -N=N- related vibrational modes of DMAB. The silver nanoparticles could be assembled together to form different size of aggregates with different concentration of PATP solution. When the concentration of Ag nanoparticle (the radius 40 nm) in colloid is 35 pM, the time-dependent SERS of DMAB reveals that the better experimental conditions for observing SERS signals of DMAB are (1) concentration of PATP is around 5 x 10(-6) M in which condition the aggregates consist with about 3-5 silver nanoparticles, which are not too big and suitable for SERS measurement, and (2) the Raman signal will be strongest at the time delay about 27 min for this concentration. By analyzing the symmetry of strong enhanced vibrational modes, it is derived that all of six strong vibrational modes are mostly enhanced by surface plasmons (electromagnetic field). The SERS enhancement calculated with finite-difference time-domain method is on the order of |M|(4) = 9.0 x 10(8) in junctions of AgNPs at 632.8 nm, where |M| = E(loc)/E(in), and E(loc) and E(in) are local and incident electric fields, respectively. The total chemical enhancements, including static chemical and resonant enhancements, are on the order of 10(3).

摘要

通过实验和理论相结合的方法,从银纳米粒子上通过选择性催化偶联反应生成的对氨基苯硫酚(PATP)中得到了对,对'-二巯基偶氮苯(DMAB)的表面增强拉曼散射(SERS)证据。PATP 的时间依赖性 SERS 光谱与 DMAB 的计算 SERS 光谱一致,这是通过银纳米粒子上的选择性催化偶联反应从 PATP 生成 DMAB 的直接证据。PATP 的所谓“b(2)模式”是 DMAB 的-N=N-相关振动模式。银纳米粒子可以聚集在一起,形成不同尺寸的聚集体,其浓度取决于 PATP 溶液的浓度。当胶体中 40nm 银纳米粒子(半径)的浓度为 35 pM 时,DMAB 的时间依赖性 SERS 表明观察 DMAB 的 SERS 信号的更好实验条件是:(1)PATP 的浓度约为 5 x 10(-6) M,在此条件下,聚集体由大约 3-5 个银纳米粒子组成,这些聚集体的尺寸不大,适合 SERS 测量;(2)对于该浓度,延迟约 27 分钟时拉曼信号最强。通过分析强增强振动模式的对称性,得出所有六个强振动模式主要都是由表面等离子体(电磁场)增强的。在 632.8nm 时,用有限差分时域法计算的 SERS 增强约为| M |(4) = 9.0 x 10(8),其中| M | = E(loc)/E(in),E(loc)和 E(in)分别是局部和入射电场。包括静态化学和共振增强在内的总化学增强约为 10(3)。

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