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Multiple weak interaction-assisted SERS detection platform for triadimefon.

Authors :
Li, Ran
Liu, Peipei
Shen, Shanshan
Wang, Haiyang
Lv, Haiming
Yu, Zhi
Wang, Yue
Guo, Zhinan
Chen, Lei
Xue, Xiangxin
Han, Xiaoxia
Ruan, Weidong
Song, Wei
Cheng, Jianbo
Zhao, Bing
Source :
Journal of Raman Spectroscopy. Jan2015, Vol. 46 Issue 1, p54-58. 5p.
Publication Year :
2015

Abstract

In this paper, a surface enhanced Raman spectra (SERS) detection platform for the widely used pesticide of triadimefon (TDF) is described. TDF is difficult to connect to the gold/silver SERS substrate, but the optical properties of the probe molecule 4-mercaptobenzoic acid (4-MBA), including the peak intensity and the peak position, are easily altered by the multiple weak interaction-assisted SERS detection platform. The limit of detection (LOD) of this method is 1.0 × 10-9 M, and the linear range is from 1.0 × 10-6 M to 1.0 × 10-9 M. The linear region is from 1.0 × 10-6 M to 1.0 × 10-9 M, described by the equation y = 884.01x + 2.24 with a correlation coefficient ( R2) of 0.9990. Interference of foreign metal ions with higher concentrations than common mineral water is too weak to the determination. Furthermore, physical insights into the phenomena and the detection mechanism were obtained and investigated theoretically. The preferential conformation of the complex and reduced density gradient (RDG) calculation results indicated that the interactions between TDF and 4-MBA consisted of multiple weak interactions through two hydrogen bonds and one van der Waals interaction. The intermolecular interaction was negative for the charge transfer from the SERS substrate to the probe molecule; thus, the peak intensity decreased. TDF interacts directly with the carboxyl of the probe molecule and consequently has an effect on the ring vibrations. Copyright © 2014 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03770486
Volume :
46
Issue :
1
Database :
Academic Search Index
Journal :
Journal of Raman Spectroscopy
Publication Type :
Academic Journal
Accession number :
100576477
Full Text :
https://doi.org/10.1002/jrs.4594