Chemistry Department, Faculty of Science, Suez Canal University, Ismailia 41522, Egypt.
Anal Chim Acta. 2013 Jan 8;759:81-91. doi: 10.1016/j.aca.2012.10.045. Epub 2012 Nov 12.
Luminescence quenching of a novel long lived Eu(III)-pyridine-2,6-dicarboxylic acid probe of 1:2 stoichiometric ratio has been studied in 0.10 volume fraction ethanol-water mixture at pH 7.5 (HEPES buffer) in the presence of the organophosphorus pesticides chlorfenvinphos (P1), malathion (P2), azinphos (P3), and paraxon ethyl (P4). The luminescence intensity of Eu(III)-(PDCA)(2) probe decreases as the concentration of the pesticide increases. It was observed that the quenching due to P3 and P4 proceeds via both diffusional and static quenching processes. Direct methods for the determination of the pesticides under investigation have been developed using the luminescence quenching of Eu(III)-pyridine-2,6-dicarboxylic acid probe in solution. The linear range for determination of the selected pesticides is 1.0-35.0 μM. The detection limits were 0.24-0.55 μM for P3, P4, and P1 and 2.5 μM for P2, respectively. The binding constants (K), and thermodynamic parameters of the OPs with Eu(III)-(PDCA)(2) were evaluated. Positive and negative values of entropy (ΔS) and enthalpy (ΔH) changes for Eu(III)-(PDCA)(2)-P1 ternary complex were calculated. As the waters in this study do not contain the above mentioned OPs over the limit detectable by the method, a recovery study was carried out after the addition of the adequate amounts of the organophosphorus pesticides under investigation.
在 pH 7.5(HEPES 缓冲液)下,在 0.10 体积分数的乙醇-水混合物中,研究了新型长寿命 Eu(III)-吡啶-2,6-二羧酸探针(化学计量比为 1:2)的荧光猝灭,该探针存在有机磷农药氯芬磷(P1)、马拉硫磷(P2)、敌百虫(P3)和 paraxon 乙基(P4)。Eu(III)-(PDCA)(2)探针的荧光强度随着农药浓度的增加而降低。观察到由于 P3 和 P4 的猝灭,既通过扩散又通过静态猝灭过程进行。使用溶液中 Eu(III)-吡啶-2,6-二羧酸探针的荧光猝灭,开发了用于测定所研究的农药的直接方法。所研究的选定农药的测定线性范围为 1.0-35.0 μM。检测限分别为 P3、P4 和 P1 的 0.24-0.55 μM 和 P2 的 2.5 μM。评估了 OPs 与 Eu(III)-(PDCA)(2)的结合常数(K)和热力学参数。计算了 Eu(III)-(PDCA)(2)-P1 三元配合物的熵(ΔS)和焓(ΔH)变化的正值和负值。由于在该研究中水中不含有该方法可检测到的上述 OPs,因此在添加适量的所研究的有机磷农药后进行了回收研究。