Chiral Pesticides with Asymmetric Sulfur: Extraction, Separation, and Determination in Different Environmental Matrices

被引:13
|
作者
Lopez-Cabeza, Rocio [1 ,2 ]
Francioso, Antonio [1 ,3 ]
机构
[1] Univ La Laguna, Inst Univ Bioorgan Antonio Gonzalez, Dept Quim Organ, Ave Astrofisico Francisco Sanchez 2, San Cristobal la Laguna 38206, Spain
[2] Inst Recursos Nat & Agrobiol Sevilla, IRNAS, CSIC, Ave Reina Mercedes 10, Seville 41012, Spain
[3] Sapienza Univ Roma, Dipartimento Chim Biol A Rossi Fanelli, Ple Aldo Moro 5, I-00185 Rome, Italy
关键词
chirality; asymmetric sulfur; enantioselectivity and stereoselectivity; pesticides; extraction methods; chromatographic techniques; capillary electrophoresis; mass spectrometry; SIMULTANEOUS ENANTIOSELECTIVE DETERMINATION; PERFORMANCE LIQUID-CHROMATOGRAPHY; ORGANOPHOSPHORUS PESTICIDES; STEREOSELECTIVE SEPARATION; NEONICOTINOID SULFOXAFLOR; GAS-CHROMATOGRAPHY; INSECTICIDE; ENANTIOMERS; FIPRONIL; SOIL;
D O I
10.3390/separations9020029
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Chiral pesticides with S atoms as asymmetric centers are gaining great importance in the search for new pesticides with new modes of action. As for the rest of the chiral pesticides, the determination of the stereoisomers separately has become crucial in the environmental risks assessment of these pesticides. Therefore, the development of suitable extraction and clean-up methods as well as efficient stereoselective analytical techniques for stereoisomers determination in environmental samples is essential. Currently, liquid/solid phase extraction, microextraction, and QuEChERS-based methods are most commonly used to obtain chiral pesticides from environmental samples. Gas, liquid, and supercritical fluid chromatography together with capillary electrophoresis techniques are the most important for the determination of the stereoisomers of chiral pesticides containing S atoms in its structure. In this study, all these techniques are briefly reviewed, and the advantages and disadvantages of each are discussed.
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页数:19
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