info:eu-repo/semantics/article
Enantioseparation of the racemates of a number of pesticides on a silica-based column with immobilized amylose tris(3-chloro-5-methylphenylcarbamate)
Fecha
2019-09Registro en:
Diaz Merino, Matias Ezequiel; Echevarria, Romina Noel; Lubomirsky, Ester; Padró, Juan Manuel; Castells, Cecilia Beatriz Marta; Enantioseparation of the racemates of a number of pesticides on a silica-based column with immobilized amylose tris(3-chloro-5-methylphenylcarbamate); Elsevier Science; Microchemical Journal; 149; 9-2019; 1-9
0026-265X
CONICET Digital
CONICET
Autor
Diaz Merino, Matias Ezequiel
Echevarria, Romina Noel
Lubomirsky, Ester
Padró, Juan Manuel
Castells, Cecilia Beatriz Marta
Resumen
We report here the results from studies on the high-performance liquid chromatographic HPLC enantioresolution of thirty different types of pesticides on the chiral silica-based column with immobilized amylose tris(3-chloro-5-methylphenylcarbamate (ACMPC) (CHIRALPAK IG-3) under polar-organic and reversed-phase conditions measured at 20 °C. The main objective was to explore diverse polar and aqueous-based eluents for use with a single column to obtain an enantioseparation of polar pesticides usually found in environmental matrices. These pesticides included phenoxy- and aryloxyphenoxypropionic acids, imidazolinones, and diphenyl-ether herbicides; acylanilides, triazoles, and pyrimidine fungicides; chlordane and pyrethroid insecticides; organophosphorus compounds; and some metabolites and precursors. We obtained improved chromatographic enantioresolutions for seventeen of these compounds in either the polar-organic or reversed-phase modes, including six pesticides whose enantioseparation is reported for first time through the use of these chromatographic modes.