Issue 7, 2014

Contribution of hydrogen bonding to charge-transfer induced surface-enhanced Raman scattering of an intermolecular system comprising p-aminothiophenol and benzoic acid

Abstract

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.

Graphical abstract: Contribution of hydrogen bonding to charge-transfer induced surface-enhanced Raman scattering of an intermolecular system comprising p-aminothiophenol and benzoic acid

Supplementary files

Article information

Article type
Paper
Submitted
18 Nov 2013
Accepted
06 Dec 2013
First published
09 Dec 2013

Phys. Chem. Chem. Phys., 2014,16, 3153-3161

Contribution of hydrogen bonding to charge-transfer induced surface-enhanced Raman scattering of an intermolecular system comprising p-aminothiophenol and benzoic acid

Y. Wang, W. Ji, Z. Yu, R. Li, X. Wang, W. Song, W. Ruan, B. Zhao and Y. Ozaki, Phys. Chem. Chem. Phys., 2014, 16, 3153 DOI: 10.1039/C3CP54856B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements