Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Quantitation Of isomeric ethyl pyridine mixtures by multivariate calibration applied to ion-molecule reaction/collision-induced dissociation triple-stage mass spectra
Author: Zampronio, CG
Moraes, LAB
Eberlin, MN
Poppi, RJ
Abstract: In reactions of the distonic ion +CH2-O-CH2. With the three isomeric ethyl pyridines, ionized methylene transfer occurs readily yielding distonic N-methylene-ethylpyridinium ions. Online mass selection and 10 eV collision-induced dissociation (CID) of the CH2+. transfer products yields characteristic fragment ions, which are formed via processes greatly influenced by the ortho, meta or para location of the ethyl substituent in the pyridine ring. Quantitation of mixtures of isomeric 2-, 3-, and 4-ethyl pyridines of varying compositions was then performed by multivariate calibration in the form of the partial least square (PLS) model applied to both single-stage (MS) 70 eV electron ionization (EI) and pentaquadrupole triple-stage sequential ion-molecule reaction/CID product ion mass spectra. The results exemplify the superior ability of combined chemometric analysis and sequential mass spectrometric techniques, which benefits from both characteristic ion chemical reactivity and dissociation behavior, for rapid and accurate quantitation of complex isomeric mixtures. (C) 2003 Elsevier Science B.V. All rights reserved.
Subject: ion-molecule reactions
sequential analysis
multivariate calibration
pentaquadrupole mass spectrometry
isomer distinction
Country: Holanda
Editor: Elsevier Science Bv
Citation: Talanta. Elsevier Science Bv, v. 60, n. 1, n. 37, n. 44, 2003.
Rights: fechado
Identifier DOI: 10.1016/S0039-9140(03)00045-6
Date Issue: 2003
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
WOS000183183800006.pdf229.89 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.