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  • 1
    ISSN: 0749-1581
    Keywords: tert-Butyl alcohol ; Dehydration ; H-ZSM-5 zeolite ; 2H NMR ; Molecular mobility ; Diffusion ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The molecular mobility and dehydration reaction of tert-butyl alcohol, selectively deuteriated in the methyl groups (t-BuOH[2 - 2H9], dTBA), absorbed on H-ZSM-5 zeolite was studied using 2H NMR spectroscopy. At 173-298 K two modes of fast anisotropic motion were observed for the adsorbed alcohol: rotation of CD3 groups around the C—C bonds and rotation of the entire (CD3)3C fragment around the C—O bond. The influence of the walls of the H-ZSM-5 channels on the geometry of adsorbed dTBA is small, the increase in the CD3—C—O angle not exceeding 2.7 ± 1.2° compared with the same angle in solid dTBA. This is explained by location of the alcohol molecules at channel intersections of the zeolite, whose dimensions exceed those of the dTBA molecule. The lifetime of the dTBA molecule at these adsorption sites exceeds 1 × 10-5 s. The observed reaction products are deuteriated water with an unusual 2H NMR lineshape and two types of butene oligomers: less mobile species with the lineshape typical of solid-state 2H NMR and more mobile species with a liquid-like lineshape. The number of more mobile species increases with increase in temperature. In addition, 2H NMR indicates the presence of tert-butyl groups in the reaction products. For oligomers with a liquid-like lineshape, the diffusion coefficient D is 3 × 10-13 m2 s-1 at 373 K, whereas for oligomers with a solid-like lineshape D ≪ 5 × 10-14 m2 s-1 at 173-373 K. The diffusion coefficient for the t-BuOH molecule was estimated as D ≪ 2 × 10-14 m2 s-1 within the temperature range 173-296 K.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0886-9383
    Keywords: Abstract factor analysis ; Target transformation factor analysis ; Signal-to-noise ratios ; Canonical variates analysis ; 13C NMR spectroscopy ; Mixture constituent identification and estimation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The theory of experimental error in analysis of mixture experiments by abstract factor analysis or target transformation factor analysis is considered. The theoretical implications of using signal-to-noise ratios (as weights) or canonical variates analysis to reduce the level of imbedded error in the factor model are examined. The approach is illustrated by application to 13C NMR spectra of lubricant basestock mixtures.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 5 (1982), S. 583-584 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Diazomethane generation ; Derivatization with diazomethane ; Methylation in microliter volumes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 11 (1988), S. 110-113 
    ISSN: 0935-6304
    Keywords: Gas chromatography, GC ; Capillary column ; Cyclodextrin stationary phase ; Isomer separation ; Enantiomer pair separation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 10 (1987), S. 105-107 
    ISSN: 0935-6304
    Keywords: Gas chromatography (GC) ; Capillary column ; Permethylated β-cyclodextrin stationary phase ; Positional isomers separation ; Enantiomer pair separation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 10 (1987), S. 156-157 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary columns ; Polytetrafluoroethylene (PTFE) joints ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Evidence as to the nature of the molecular ions of the title compounds near the ionization thresholds and of their fragmentation processes is presented and discussed. The mode of formation of 5-membered rings, involving the loss of an ortho substituent, is compared and contrasted with the formally similar process reported for the N-dimethyl N'-(o-X-phenyl) formamidines.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 13 (1978), S. 218-223 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electron impact studies on eight α,β-unsaturated carbonyl oximes revealed many interesting hydrogen and skeletal rearrangements which were substantiated by deuterium labelling, exact mass measurements and metastable studies. Loss of H· and OH· as well as formation of the indenyl and fluorenyl cations and the [C9H6N]+ fragment proceed through cyclic intermediates. All the ionized oximes undergo a Beckmann rearrangement in the gaseous phase leading to intense aroyl cation peaks. Formation of the styrene radical ions and cleavage of the bond α to the oxime function have also been noticed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 14 (1979), S. 239-243 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Examination of the mass spectra of eleven 2-arylhydrazonopropandioic acid derivatives reveals that a radical ion which is tentatively formulated as a 1H-diazirine species is produced in each case (except for the diphenyl este) by more than one process. Formation of what is formally the aryl amine radical ion occurs by a novel hydrogen rearrangement. Simple cleavage of the bonds β to either the aromatic ring or the C=N moiety also produces abundant ions. The diphenyl ester behaves anomalously yielding the phenol ion instead of the amine. The proposed mechanisms were confirmed by metastable studies, deuterium labelling and exact mass measurements.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 1 (1968), S. 567-581 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of twenty one C-19 modified cholesteryl derivatives have been determined and compared with results for related systems. In the case when the hydrogen(s) of the C-19 group have been replaced by other groups the metastable evidence shows that in those molecules with a C-3 hydroxyl group the loss of water followed by the loss of the C-19 group gives rise to an intense ion at m/e 353, whereas the loss of the C-19 group with hydrogen transfer to the ion, followed by the loss of water gives rise to the large ion at m/e 354. In contrast in the case of the C-3 acetates the main fragmentation is the loss of acetic acid followed by the loss of the C-19 group to give the ion at m/e 353. This is rationalised on the basis of results observed in other systems. In the case of the C-3 tosylates evidence for pyrolysis before electron impact fragmentation is presented. The subsequent fragmentation of the large ions at m/e 354, 353 and other m/e values in the high mass region is shown to be in line with earlier work.
    Additional Material: 22 Ill.
    Type of Medium: Electronic Resource
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