Contribution of hydrogen bonding to charge-transfer induced surface-enhanced Raman scattering of an intermolecular system comprising p-aminothiophenol and benzoic acid
Literature Information
Yue Wang, Wei Ji, Zhi Yu, Ran Li, Xu Wang, Wei Song, Weidong Ruan, Bing Zhao, Yukihiro Ozaki
We investigated the influence of hydrogen bonds (H-bonds) on the intermolecular interactions of a system comprising p-aminothiophenol (PATP) and benzoic acid (BA) using surface-enhanced Raman scattering (SERS) for the first time. In this system, H-bonds form through intermolecular interactions between the –NH2 and –COOH groups and promote the charge-transfer (CT) transition from the Ag substrate to the adsorbed PATP molecules. Accordingly, the intensities of the non-totally symmetric vibrations (the b2-type bands) of PATP are influenced through the Herzberg–Teller contribution. This is clearly a BA concentration-dependent phenomenon. This behaviour can be attributed to an increase in the degree of conjugation of the system, which facilitates the CT process in the system with H-bonds. Furthermore, temperature-dependent SERS experiments and their two-dimensional (2D) correlation analysis confirmed that the formation of H-bonds facilitated the CT transition between the adsorbed molecules and substrate. The degree of CT was reduced by H-bond breakage that occurred with increasing temperature. An additional SERS experiment involving substituted BA molecules yielded similar conclusions.
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