Atmospheric pressure photoionization mechanisms. 2. The case of benzene and toluene

被引:67
作者
Tubaro, M [1 ]
Marotta, E [1 ]
Seraglia, R [1 ]
Traldi, P [1 ]
机构
[1] CNR, Ist Sci & Tecnol Mol, Sez Padova, I-35127 Padua, Italy
关键词
D O I
10.1002/rcm.1208
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Benzene and toluene have been proposed previously as dopants in atmospheric pressure photoionization (APPI) experiments on compounds exhibiting ionization energies higher than the energy of photons used for irradiation. Their low ionization energies lead to their easy photoionization and the ions so formed lead to the ionization of analytes through charge exchange. However, some measurements have shown that some protonation reactions also take place, and a series of experiments was undertaken to investigate this unexpected behavior. It was shown that, when benzene is irradiated in the APPI source, the odd-electron molecular ions of phenol, diphenyl ether and phenoxyphenol are produced in high yield, together with protonated diphenyl ether and protonated phenoxyphenol. These results have been confirmed by deuterium labelling and MSn experiments. A possible mechanism is proposed, based on a radical attack by benzene molecular ions on oxygen molecules present inside the APPI source, analogous to that proposed in the literature for phenyl radicals. Similar results have been obtained with toluene, proving that APPI is able to activate a series of reactions leading to highly reactive species which are highly effective in promoting ionization of molecules with ionization energies higher than the photon energy. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:2423 / 2429
页数:7
相关论文
共 21 条
[1]  
ATKINSON R, 1994, J PHYS CHEM REF DATA, pR1
[2]   EVALUATED KINETIC AND PHOTOCHEMICAL DATA FOR ATMOSPHERIC CHEMISTRY SUPPLEMENT-IV - IUPAC SUBCOMMITTEE ON GAS KINETIC DATA EVALUATION FOR ATMOSPHERIC CHEMISTRY [J].
ATKINSON, R ;
BAULCH, DL ;
COX, RA ;
HAMPSON, RF ;
KERR, JA ;
TROE, J .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1992, 21 (06) :1125-1568
[3]  
Atkinson R., 1989, J. Phys. Chem. Ref. Data, V1, P1
[4]  
Harrison A. G., 1983, CHEM IONIZATION MASS
[5]  
HARTMAN KN, 1979, 791777 NBSIR DEP COM
[6]   Evaluated gas phase basicities and proton affinities of molecules: An update [J].
Hunter, EPL ;
Lias, SG .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1998, 27 (03) :413-656
[7]   Atmospheric pressure photoionization mass spectrometry. Ionization mechanism and the effect of solvent on the ionization of naphthalenes [J].
Kauppila, TJ ;
Kuuranne, T ;
Meurer, EC ;
Eberlin, MN ;
Kotiaho, T ;
Kostiainen, R .
ANALYTICAL CHEMISTRY, 2002, 74 (21) :5470-5479
[8]   Surface-assisted reduction of aniline oligomers, N-phenyl-1,4-phenylenediimine and thionin in atmospheric pressure chemical ionization and atmospheric pressure photoionization [J].
Kertesz, V ;
Van Berkel, GJ .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2002, 13 (02) :109-117
[9]   Comparison of electrospray, atmospheric pressure chemical ionization, and atmospheric pressure photoionization in the identification of apomorphine, dobutamine, and entacapone phase II metabolites in biological samples [J].
Keski-Hynnilä, H ;
Kurkela, M ;
Elovaara, E ;
Antonio, L ;
Magdalou, J ;
Luukkanen, L ;
Taskinen, J ;
Kostiainen, R .
ANALYTICAL CHEMISTRY, 2002, 74 (14) :3449-3457
[10]  
KOSTER G, 2001, P 47 ASMS C MASS SPE