Multiphoton ionization of nitrotoluenes by means of ultrashort laser pulses

被引:15
|
作者
Tönnies, K
Schmid, RP
Weickhardt, C
Reif, J
Grotemeyer, J
机构
[1] Univ Kiel, Inst Phys Chem, D-24098 Kiel, Germany
[2] Brandenburg Tech Univ Cottbus, Lehrstuhl Phys Chem & Analyt, D-03044 Cottbus, Germany
[3] Brandenburg Tech Univ Cottbus, Lehrstuhl Expt Phys 2, D-03044 Cottbus, Germany
关键词
multiphoton ionization; mass spectrometry; ultra short laser pulses; nitrotoluenes; explosives;
D O I
10.1016/S1387-3806(00)00374-2
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
The potential of ultrashort laser pulses in the laser mass spectrometry of photounstable molecules is demonstrated for the case of nitrotoluenes. Nitro compounds tend to quickly dissociate after photoexcitation producing only unspecific fragments under conventional nanosecond multiphoton ionization conditions. The mass spectra of two isomers of mononitrotoluene, two isomers of dinitrotoluene and trinitrotoluene were recorded following multiphoton ionization with 170 fs laser pulses either with a wavelength of 412 or 206 nm. Although even these laser mass spectra are characterized by intense fragmentation they exhibit a clear molecular ion or OH loss signals depending on the substitution positions. Although the two mononitrotoluenes can be distinguished by their mass spectra at both wavelengths the two isomers of dinitrotoluene investigated show characteristic features which allow their clear differentiation only at 412 nm. (Int J Mass Spectrom 206 (2001) 245-250) (C) 2001 Elsevier Science B.V.
引用
收藏
页码:245 / 250
页数:6
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