Electron affinities of polynuclear aromatic hydrocarbons and negative-ion chemical-ionization sensitivities

被引:8
作者
Betowski, L. D.
Enlow, Mark
Aue, Donald H.
机构
[1] US EPA, NERL, Las Vegas, NV 89193 USA
[2] Appl Res Associates Inc, Tyndall AFB, FL 32403 USA
[3] Univ Calif Santa Barbara, Dept Chem, Santa Barbara, CA 93106 USA
关键词
polynuclear aromatic hydrocarbon (PAH); electron affinity; chemical-ionization mass spectrometry; computational chemistry;
D O I
10.1016/j.ijms.2006.04.008
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Negative-ion chemical-ionization mass spectrometry (NICI MS) has the potential to be a very useful technique in identifying various polycyclic aromatic hydrocarbons (PAHs) in soil and sediment samples. Some PAHs give much stronger signals under NICI MS conditions than others. On the other hand, positive-ion signals are largely comparable under the same source conditions. An extensive set of newly re-evaluated experimental electron affinities (EAs), or free energies of electron attachment, are now available, as well as reliable predicted electron affinities from quantum theoretical calculations or from solution reduction potentials and theoretically predicted solvation energies. In order to show a high negative-ion sensitivity, a PAH must have an EA that exceeds a threshold of approximately of 0.5 eV Comparisons between the negative-ion to positive-ion sensitivities (N/P ratios) and these new electron affinities show a rough correlation between the two, but naphthacene and perylene are exceptions to this relationship with much lower sensitivities than expected from their high EA values. By calculating the EA for a PAH, one can predict whether a sensitivity enhancement under NICI MS conditions is to be expected. Since aliphatic hydrocarbons and many other substances have negative or very low EAs, NICI MS is expected to be a good technique for detecting PAHs in samples contaminated with other hydrocarbons or compounds with low EAs. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 129
页数:7
相关论文
共 46 条
[41]  
Su T., 1973, International Journal of Mass Spectrometry and Ion Physics, V12, P347, DOI 10.1016/0020-7381(73)80104-4
[42]   ION-POLAR MOLECULE COLLISIONS - PROTON-TRANSFER REACTIONS OF H3+ AND CH5+ TO GEOMETRIC ISOMERS OF DIFLUOROETHYLENE, DICHLOROETHYLENE, AND DIFLUOROBENZENE [J].
SU, T ;
BOWERS, MT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1973, 95 (05) :1370-1373
[43]  
Szabo A., 2012, Modern quantum chemistry: introduction to advanced electronic structure theory
[44]   POLYCYCLIC AROMATIC-HYDROCARBONS - NEGATIVE-ION FORMATION FOLLOWING LOW-ENERGY (0-15 EV) ELECTRON-IMPACT [J].
TOBITA, S ;
MEINKE, M ;
ILLENBERGER, E ;
CHRISTOPHOROU, LG ;
BAUMGARTEL, H ;
LEACH, S .
CHEMICAL PHYSICS, 1992, 161 (03) :501-508
[45]   Effect of buffer gas alterations on the thermal electron attachment and detachment reactions of azulene by pulsed high pressure mass spectrometry [J].
Williamson, DH ;
Knighton, WB ;
Grimsrud, EP .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2000, 195 :481-489
[46]  
1988, POLYCYCLIC AROMATIC