Resonance Rayleigh scattering, second-order scattering and frequency doubling scattering spectra for studying the interaction of erythrosine with Fe(phen)32+ and its analytical application

被引:16
|
作者
Liu, Jin Fang [1 ]
Li, Nian Bing [1 ]
Luo, Hong Qun [1 ]
机构
[1] Southwest Univ, Key Lab Luminescence & Real Time Anal, Minist Educ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
Erythrosine; Fe(phen)(3)(2+); Resonance Rayleigh scattering; Second-order scattering; Frequency doubling scattering; LIGHT-SCATTERING; AMINOGLYCOSIDE ANTIBIOTICS; SILVER NANOPARTICLES; GOLD NANOPARTICLES; CRYSTAL VIOLET; DYES; SYSTEM; ASSAY; ACID; HYDROCHLORIDE;
D O I
10.1016/j.saa.2011.03.046
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
In a weak alkaline Britton-Robinson buffer medium, erythrosine (Ery) can react with Fe(phen)(3)(2+) to form 1:1 ion-association complex, which will cause not only the changes of the absorption spectra, but also the remarkable enhancement of resonance Rayleigh scattering (RRS), second-order scattering (SOS) and frequency doubling scattering (FDS) spectra, and the appearance of new spectra of RRS. SOS and FDS. The maximum RRS, SOS and FDS wavelengths (lambda(ex)/lambda(em)) of the ion-association complex are located at 358/358 nm, 290/580 nm and 7801390 nm, respectively. The increments of scattering intensities (Delta I) are directly proportional to the concentration of Ery in a certain range. The detection limits for Ery are 0.028 mu g mL(-1) for RRS method, 0.068 mu g mL(-1) for SOS method and 0.11 mu g mL(-1) for FDS method, respectively. Among them, the RRS method has the highest sensitivity. Based on the above researches, a new highly sensitive and simple method for the determination of Ery has been developed. In this work, the spectral characteristics of absorption. RRS, SOS and FDS spectra, the optimum conditions of the reaction and influencing factors for the RRS. SOS and FDS intensities were investigated. In addition, the reaction mechanism was discussed. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:631 / 637
页数:7
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