{"title":"UV MULTIPHOTON INDUCED CHEMISTRY OF NITROBENZENE IN SOLUTION","authors":"J. BelBruno, G. Siuzdak, S. North","doi":"10.1155/1990/42676","DOIUrl":null,"url":null,"abstract":"The technique of Multiphoton Induced Chemistry (MPIC) has been employed to initiate ion-molecule \nchemistry of organic molecules in solution. We report one of the first examples of the use of liquid phase \nmultiphoton ionization (MPI) to prepare organic cations, which then react with the solvent in ionmolecule \nprocesses. The products obtained in this chemical sequence are significantly different from those \nobserved in conventional or multiphoton-induced neutral chemistry in the same solvent. The particular \nexample explored in this work is the reactivity of the nitrobenzene cation in methanol solvent. Products of \nthe ion-molecule chemistry, detected by gas chromatography/mass spectrometry, are phenol and benzyl \nalcohol. These products depend upon the square of the laser intensity. It is shown by ionization current \nmeasurements in a conductance cell, that ionic species are produced as precursors to the observed \nproducts. The implications of this application of MPI are briefly discussed. A preliminary report on the \nunimolecular chemistry of the highly excited neutral molecule is also included. The product of this channel \nis nitrosobenzene. It is shown, in this case, that the reactive state is most likely a highly vibrationally \nexcited ground state molecule, not the lowest triplet level invoked in conventional photochemistry.","PeriodicalId":296295,"journal":{"name":"Laser Chemistry","volume":"21 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laser Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/1990/42676","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
The technique of Multiphoton Induced Chemistry (MPIC) has been employed to initiate ion-molecule
chemistry of organic molecules in solution. We report one of the first examples of the use of liquid phase
multiphoton ionization (MPI) to prepare organic cations, which then react with the solvent in ionmolecule
processes. The products obtained in this chemical sequence are significantly different from those
observed in conventional or multiphoton-induced neutral chemistry in the same solvent. The particular
example explored in this work is the reactivity of the nitrobenzene cation in methanol solvent. Products of
the ion-molecule chemistry, detected by gas chromatography/mass spectrometry, are phenol and benzyl
alcohol. These products depend upon the square of the laser intensity. It is shown by ionization current
measurements in a conductance cell, that ionic species are produced as precursors to the observed
products. The implications of this application of MPI are briefly discussed. A preliminary report on the
unimolecular chemistry of the highly excited neutral molecule is also included. The product of this channel
is nitrosobenzene. It is shown, in this case, that the reactive state is most likely a highly vibrationally
excited ground state molecule, not the lowest triplet level invoked in conventional photochemistry.