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吸附在胶体银颗粒上的2,2'-联喹啉的表面增强拉曼散射。

Surface enhanced Raman scattering of 2,2' biquinoline adsorbed on colloidal silver particles.

作者信息

Chowdhury J, Ghosh M, Misra T N

机构信息

Department of Spectroscopy, Indian Association for the Cultivation of Science, Calculta.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2000 Oct;56A(11):2107-15. doi: 10.1016/s1386-1425(00)00263-8.

Abstract

Surface enhanced Raman scattering (SERS) in silver sol and normal Raman spectra in the bulk and in solution of 2,2' biquinoline (BQ) molecule have been investigated. The observed Raman bands along with their corresponding FTIR bands have been assigned based on the established assignments of the vibrational bands of the parent napthalene and quinoline molecules. Existence of both the cis and trans form of the BQ molecule in solution and in the bulk are inferred from the normal Raman and FTIR spectra, whereas SERS study reveal that in the surface adsorbed state the molecule exists in the cis form. Definite evidence of the charge transfer interaction to the overall contribution in the SER enhancement have been reported. The excitation profile also supports the CT interaction. Estimated enhancement factor of the principal SERS bands indicate that the molecule is adsorbed on the silver surface through both the nitrogen atoms with the molecular plane almost perpendicular to the surface. This preferred orientation of the molecule is in conformity with its existence in the cis form in the surface adsorbed state.

摘要

研究了2,2'-联喹啉(BQ)分子在银溶胶中的表面增强拉曼散射(SERS)以及其本体和溶液中的正常拉曼光谱。基于母体萘和喹啉分子振动带的既定归属,对观察到的拉曼带及其相应的傅里叶变换红外(FTIR)带进行了归属。从正常拉曼光谱和FTIR光谱推断出BQ分子在溶液和本体中同时存在顺式和反式结构,而SERS研究表明,在表面吸附状态下,该分子以顺式形式存在。已报道了电荷转移相互作用对SERS增强总体贡献的确切证据。激发谱也支持电荷转移相互作用。主要SERS带的估计增强因子表明,该分子通过两个氮原子吸附在银表面,分子平面几乎垂直于表面。分子的这种优先取向与其在表面吸附状态下以顺式形式存在相一致。

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