Chemical ionization pathways of polyfluorinated chemicals - A connection to environmental atmospheric processes

被引:24
作者
Ellis, DA [1 ]
Mabury, SA [1 ]
机构
[1] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
关键词
D O I
10.1016/S1044-0305(03)00450-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A systematic mass spectrometry study of an industrially prolific class of polyfluorinated compounds known as telomers was conducted. The study specifically focused upon polyfluorinated alcohols along with corresponding saturated and alpha,beta-unsaturated fluoroacids. Within each class differing fluoroalkyl chain length homologues were investigated, using negative and positive chemical ionization mass spectrometry (NCI and PCI). In the case of the fluoroalcohols, NCI resulted in the production of more elaborate spectra than the other classes. Moreover, it showed the interesting production of HF2- and the complex of this species, along with F-, with the parent molecule. These complexes resulted in the formation of the novel H2F3- ion. Results show that there is significant intra-molecular hydrogen bonding that occurs for these compounds, which influences the molecules fragmentation. This bonding will also influence the fate and disposition through environmental processes (e.g., V-P, k(OH), K-OA) which are affected by molecular geometry. Furthermore, there is an increased accumulation and persistence potential for the molecule as a function of the fluorocarbon chain length. We have shown that in conjunction with the use of mass spectroscopy the engertics of environmental processes for polyfluorinated materials can be established. (C) 2003 American Society for Mass Spectrometry.
引用
收藏
页码:1177 / 1191
页数:15
相关论文
共 44 条
[31]   Electron photodetachment spectroscopy of solvated anions: RO center dot HF- or ROH center dot F-? [J].
Mihalick, JE ;
Gatev, GG ;
Brauman, JI .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (49) :12424-12431
[32]   Determination of perfluorinated surfactants in surface water samples by two independent analytical techniques:: Liquid chromatography/tandem mass spectrometry and 19F NMR [J].
Moody, CA ;
Kwan, WC ;
Martin, JW ;
Muir, DCG ;
Mabury, SA .
ANALYTICAL CHEMISTRY, 2001, 73 (10) :2200-2206
[33]   MASS-SPECTROMETRY OF SOME C6F13-COMPOUNDS AND THEIR C6H13-ANALOGS [J].
NAPOLI, M ;
KROTZ, L ;
SCIPIONI, A ;
SERAGLIA, R ;
TRALDI, P .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1993, 7 (09) :789-794
[34]   MASS-SPECTROMETRIC STUDIES ON SOME F(CF2)N(CH2)MH SEMIFLUORINATED ALKANES [J].
NAPOLI, M ;
KROTZ, L ;
CONTE, L ;
SERAGLIA, R ;
TRALDI, P .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1993, 7 (11) :1012-1016
[35]   Comparison of the toxicokinetics between perfluorocarboxylic acids with different carbon chain length [J].
Ohmori, K ;
Kudo, N ;
Katayama, K ;
Kawashima, Y .
TOXICOLOGY, 2003, 184 (2-3) :135-140
[36]   A MASS-SPECTROMETRIC STUDY OF POSITIVE AND NEGATIVE-ION FORMATION IN AN SF6 CORONA .1. SOURCES OF SULFUR-FLUORIDE IONS [J].
SAUERS, I ;
HARMAN, G .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 1992, 25 (05) :761-773
[37]  
Schlosser M, 1998, ANGEW CHEM INT EDIT, V37, P1497
[38]  
Smart B.E., 1986, MOL STRUCTURE ENERGE, P141
[39]   Fluorine substituent effects (on bioactivity) [J].
Smart, BE .
JOURNAL OF FLUORINE CHEMISTRY, 2001, 109 (01) :3-11
[40]  
STOCK NL, UNPUB