Cluster chemical ionization and deuterium exchange mass spectrometry in supersonic molecular beams

被引:24
作者
Dagan, S [1 ]
Amirav, A [1 ]
机构
[1] TEL AVIV UNIV,SCH CHEM,SACKLER FAC EXACT SCI,IL-69978 TEL AVIV,ISRAEL
关键词
D O I
10.1016/1044-0305(96)00017-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A cluster-based chemical ionization method has been developed that produces protonated molecular ions from molecules introduced through a supersonic molecular beam interface. Mixed clusters of the analyte and a clustering agent (water or methanol) are produced in the expansion region of the beam, and are subsequently ionized by ''fly through'' electron impact (EI) ionization, which results in a mass spectrum that is a combination of protonated molecular ion peaks together with the conventional EI fragmentation pattern. The technique is presented and discussed as a tool complementary to electron impact ionization in supersonic molecular beams. Surface-induced dissociation on a rhenium oxide surface is also applied to simplify the mass spectra of clusters and reveal the analyte spectrum. The high gas flow rates involved with the supersonic molecular beam interface that enable the easy introduction of the clustering agents also have been used to introduce deuterating agents. An easy-to-use, fast, and routine on-line deuterium exchange method was developed to exchange active hydrogens (NH, OH). This method, combined with electron impact ionization, is demonstrated and discussed in terms of the unique information available through the EI fragmentation patterns, its ability to help in isomer identification, and possible applications with fast gas chromatography-mass spectrometry in supersonic molecular beams.
引用
收藏
页码:550 / 558
页数:9
相关论文
共 29 条
[11]   HIGH-EFFICIENCY SURFACE-INDUCED DISSOCIATION ON A RHENIUM OXIDE SURFACE [J].
DAGAN, S ;
AMIRAV, A .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1993, 4 (11) :869-873
[12]   Surface ionization mass spectrometry of drugs in the thermal and hyperthermal energy range - A comparative study [J].
Dagan, S ;
Amirav, A ;
Fuju, T .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1995, 151 (2-3) :159-165
[13]   FAST, HIGH-TEMPERATURE AND THERMOLABILE GC MS IN SUPERSONIC MOLECULAR-BEAMS [J].
DAGAN, S ;
AMIRAV, A .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1994, 133 (2-3) :187-210
[14]   ELECTRON-IMPACT MASS-SPECTROMETRY OF ALKANES IN SUPERSONIC MOLECULAR-BEAMS [J].
DAGAN, S ;
AMIRAV, A .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1995, 6 (02) :120-131
[15]  
DAGAN S, 1996, IN PRESS J AM SOC MA
[16]  
DAGAN S, 1995, P 43 ASMS M ATL, P108
[17]  
Harrison A. G., 1992, Chemical Ionization Mass Spectrometry, V2
[18]   DETERMINATION OF ACTIVE HYDROGEN IN ORGANIC COMPOUNDS BY CHEMICAL IONIZATION MASS-SPECTROMETRY [J].
HUNT, DF ;
MCEWEN, CN ;
UPHAM, RA .
ANALYTICAL CHEMISTRY, 1972, 44 (07) :1292-&
[19]   CLUSTERS OF ORGANIC-MOLECULES IN A SUPERSONIC JET EXPANSION [J].
JONKMAN, HT ;
EVEN, U ;
KOMMANDEUR, J .
JOURNAL OF PHYSICAL CHEMISTRY, 1985, 89 (20) :4240-4243
[20]   REACTIVE ION-SURFACE COLLISIONS - APPLICATION OF IONIZED ACETONE-D(6), DMSO-D(6) AND PYRIDINE-D(5) AS PROBES FOR THE CHARACTERIZATION OF SELF-ASSEMBLED MONOLAYER FILMS ON GOLD [J].
KANE, TE ;
SOMOGYI, A ;
WYSOCKI, VH .
ORGANIC MASS SPECTROMETRY, 1993, 28 (12) :1665-1673