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pro vyhledávání: '"Elizabeth P. Burrows"'
Autor:
Elizabeth P. Burrows
Publikováno v:
Journal of Mass Spectrometry. 33:221-228
Dimethyl ether (DME) is a useful reagent gas for the characterization of a variety of diverse biologically important or environmentally significant classes of compounds. In this work the gas-phase ion–molecule reactions of DME with 23 α-amino acid
Publikováno v:
Chemosphere. 31:2767-2777
Conditions have been established for H4IIE rat hepatoma cell cultures in which effects of cytochrome P-450 induction on the metabolism of a munitions wastestream pollutant can be studied. Under these conditions, the polychlorinated hydrocarbon 2,3,4,
Autor:
Elizabeth P. Burrows
Publikováno v:
Mass Spectrometry Reviews. 14:107-115
The uses of dimethyl ether (DME) as an unusual positive ion reagent for chemical ionization mass spectrometry (CIMS) are reviewed. The fragment–molecule adducts formed by ion–molecule reactions of organic substrates with the ionized gas are highl
Autor:
Elizabeth P. Burrows
Publikováno v:
Journal of Mass Spectrometry. 30:312-318
Dimethyl ether (DME) chemical ionization mass spectrometry of a number of polynuclear aromatic hydrocarbons (PAHs) gave rise to a variety of fragment–molecule adduct ions resulting from ion–molecule reactions with the reagent gas. In 18 out of 22
Publikováno v:
Environmental sciencetechnology. 16(7)
Rates of reaction of chlorine dioxide with phenol and with hydroquinone were determined with a stopped-flow spectrophotometer in the pH range 4-8. Second-order rate constants increase with increasing pH, consistent with a mechanism in which both the
Autor:
Elizabeth P. Burrows
Publikováno v:
Biological Mass Spectrometry. 23:492-498
Dimethyl ether (DME) chemical ionization mass spectrometry with introduction by direct exposure desorption has been utilized for the characterization of a group of 23 structurally diverse biologically active trichothecene toxins. Both proton adducts
Autor:
Elizabeth P. Burrows
Publikováno v:
Organic Mass Spectrometry. 29:315-320
Dimethyl ether (DME) chemical ionization mass spectrometry with introduction by direct exposure desorption was utilized for the characterization of a variety of nitramines, nitroaromatics and related compounds. For the nitramines and for many of the
Autor:
Elizabeth P. Burrows
Publikováno v:
ChemInform. 27
The uses of dimethyl ether (DME) as an unusual positive ion reagent for chemical ionization mass spectrometry (CIMS) are reviewed. The fragment–molecule adducts formed by ion–molecule reactions of organic substrates with the ionized gas are highl
Publikováno v:
Amino, Nitrosco and Nitro Compounds and Their Derivatives: Volume 2 (1982)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec9fdae7799bbc2ccc87d97fdc195628
https://doi.org/10.1002/9780470771679.ch10
https://doi.org/10.1002/9780470771679.ch10
Autor:
Elizabeth P. Burrows
Publikováno v:
Organic Mass Spectrometry. 26:1027-1031
Mass spectra of seven related N-heterocyclics, introduced by direct exposure probe, were determined in electron impact (EI) and positive- and negative-ion chemical ionization (PCI and NCI) modes. Proton adducts were the predominant molecular ion spec