Further Investigation of the Mass Spectrum of Isopropyl o-Toluate
スポンサーリンク
概要
- 論文の詳細を見る
The formation of an [M+1]+ ion and the fragmentation of isopropyl o-toluate have been further investigated by measuring the mass spectrum of CD3C6H4COOC3H7(d3). The hydrogen atom, which is involved in the [M+1]+ ion formation, originates mainly from the three methyl groups in the molecule, in contrast to the previous conclusions.In the intermediate ion at m/z 136, [C8H8O2]+, almost complete scrambling of the hydroxyl hydrogen atom with the methyl hydrogen atoms in tolyl group, not with the hydrogen atoms in benzene ring, takes place prior to the elimination of a water molecule from this m/z 136 ion. However, any hydrogen exchange reaction does not occur prior to the elimination of a hydroxy radical, which is a competing reaction with water loss, from the m/z 136 ion.Furthermore, it is shown that the metastable decomposing [C7H7]+ ion at m/z 91 isomerizes to tropylium ion prior to the decomposition of this ion into the [C5H5]+ ion at m/z 65.
- 日本質量分析学会の論文
著者
-
Tobita S
Gunma Univ. Gunma
-
Tajima Susumu
Gunma College Of Technology
-
Tsuchiya Toshikazu
Chiba Technical Institute
-
Azami Tadashige
Gunma Technical College
-
Hashimoto Hisanobu
Japan UpJohn Research Laboratories
-
Hasegawa Yoshikazu
Japan UpJohn Research Laboratories
-
Tsuchiya Toshikazu
Chiba Institute of Technology
関連論文
- Correlation between Phototoxicity and Photoionization Efficiency of Phenothiazine Drugs
- Unimolecular Decompositions of 2, 2, 2-Trifluoroethyl Acetate, 2, 2, 2-Trifluoroethyl Trifluoroacetate, and S-Ethyl Trifluorothioacetate upon Electron Impact
- γ-AMINOBUTYRIC ACID IN THE MURINE BRAIN: MASS FRAGMENTOGRAPHIC ASSAY METHOD AND POST-MORTEM CHANGES
- A Study of Hydrogen Rearrangement Reactions in the Molecular Ion of 1,2-Dimethoxyethane by MIKE Spectrometry
- Structural Study of Intermediate Ions by Kinetic Energy Release and Thermochemical Consideration: [C7H8N]+ Ions from Toluidine Derivatives
- Fragmentation Process of Benzenedicarboxylic Acid Dimethyl Esters
- Fragmentation Mechanism of p-Cyanobenzoic Acid Isopropyl Ester by Electron Impact
- A Kinetic Energy Release Study of the NO Loss from Several Substituted Nitrobenzene Molecular Ions
- An Investigation of Structure of Intermediate Ions by Kinetic Energy Release. C7H7+ Ions from Several Derivatives of Toluene
- Further Investigation of the Mass Spectrum of Isopropyl o-Toluate
- Fragmentation of Organosulfur Compounds upon Electron Impact : II. Metastable Decomposition of Methyl and Ethyl Thiolactates
- Metastable Ion Study of Organosilicon Compounds Part IV. 1,1,1,3,3,3-Hexamethyldisilazane and 1,1,3,3-Tetramethyldisilazane
- Effect of Various Target Molecules on a Charge Transfer Process C6H62+ → C6H6+
- An Investigation of Structure of Intermediate Ions from Several Substituted Alkyl Benzoates by the ortho Effect and Kinetic Energy Release
- Study on the fragmentation mechanism of isopropyl methacrylate.