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  • 1990-1994  (15)
  • Analytical Chemistry and Spectroscopy  (14)
  • Tortricidae
  • 1
    ISSN: 1573-1561
    Keywords: Trichothecenes ; sesquiterpines ; Fusarium sporotrichioides ; fungal toxins ; insecticidal activity ; fungal pathogen ; Paecilomyces farinosus ; spruce budworm ; Choristoneura fumiferana ; Lepidoptera ; Tortricidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Trichothecene mycotoxins were produced byFusarium sporotrichioides DAOM 197255 isolated from a spruce budworm cadaver. An extract from the culture filtrate containing these metabolites was toxic to budworm when ingested at concentrations as low as 10 ppm in diet, and survivors were predisposed to infection with a fungal entomopathogen. The possible role of these metabolites in the balsam fir-spruce budworm habitat is discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 17 (1994), S. 753-755 
    ISSN: 0935-6304
    Keywords: Capillary electrophoresis ; Nitrosamines ; Subambient temperature ; syn and anti isomers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The separation of a selected group of naturally occurring, heterocyclic nitrosoamino acids was achieved by capillary zone electrophoresis and the resolution of the syn and anti conformers improved as the temperature was lowered to 5 °C. The double peaks observed for each nitrosoamino acid are probably caused by the slow kinetics of conformational isomerism. The experimental setup consisted of a P/ACE 5510 electrophoresis system, a 57 cm polyacrylamidecoated capillary, and a 10 mM phosphate buffer, pH 7.2, containing 2 mM of 3-(N-N-dimethylmyristylammonio)propanesulfonate (DMMAPS) and 0.1% Tween 20. Our study shows that (a) the lower the temperature, the greater the resolution and the longer the migration times; and (b) different nitrosoamino acid conformers were resolved at different temperatures because of differences in the rate of isomerization. For example, the conformers of N-nitrosothiazolidine-4-carboxylic acid were partially resolved at 30 °C while those of N-nitrosoproline were well resolved at the same temperature.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 17 (1994), S. 102-103 
    ISSN: 0935-6304
    Keywords: HPLC ; Capillary electrophoresis (CE) ; Laser desorption mass spectrometry ; Synthetic peptides ; Purity determination ; 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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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 26 (1991), S. 1019-1022 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The energetics and mass spectral characteristics of a number of [C7H5]+ ions have been examined. No compelling evidence could be found to show that the 2-cyclopropaphenyl cation was produced by loss of bromine from the ionized 2-bromo derivative. It was proposed that the ethynylcyclopentadienyl cation may be the global minimum on the [C7H5]+ hypersurface.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 28 (1993), S. 459-462 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Unusual expulsion of ‘SO’ was observed from the molecular ions of substituted diphenyldithiocarbonates under electron impact conditions. An initial aryloxy migration to sulphur followed by further rearrangement is proposed for this process, based on the substituent effects. The diarylthioketone radical-cation structure assigned for the [M - SO] ion was confirmed through the collision-activated dissociation B/E linked-scan spectra.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is concluded that C3H8O+· formed by dissociation of ionized 2-ethoxyethanol (8) is a mixture of CH3CH2OCH3+· (7) and ·CH2+OHCH2CH3 (2). Formation of 7 and CH3CH2+OHCH3 (12) is attributed to dissociations of species formed by the hydrogen transfers [CH3CH2OCH2+ ·CH2OH] → [CH3CH2OCH2OCH3+· CH2O] → [CH3CH2+OHCH3HCO·]. Production of 7 competes weakly with dissociation to CH3CH2 +OCH2 (13) and to 12. The low abundance of 7 is attributed to the simple dissociation 8 → 13 being both energetically and entropically favored, and a second H-transfer to give 12 being energetically favored. The threshold for forming 7 is 45 kJ mol-1 above that for dissociation directly to 13, so formation of 7 is the first ion-neutral complex-mediated elimination found to have a threshold above that for the competing simple dissociation. The low abundance of 7 also demonstrates that ion-neutral complexes can be intermediates without obviously revealing their presence by direct dissociation. Experimental results suggest that 2 isomerizes to CH3CH2CH2OH+· (5) and then dissociates by eliminating water. Ab initio results support the feasibility of 2 → CH3+OHCH2CH2· (1) and 2 → 5. However, experimental observations suggest that 2 → 1 does not occur. This is attributed to strong competition from dissociation and isomerization to 5. The transition state for 2 → 5 resembles [CH3CH2CH2OH]+·, and a cyclic transition state for 2 → 5 is ruled out. When the ethyl-oxygen bond in 2 is simply lengthened, the charge is initially concentrated on ethyl, but it switches to CH2OH in a curve crossing at an apparent transition state for C—O bond breaking.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 25 (1990), S. 14-20 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A collision-induced dissociation (CID) study of five synthesized nitramines was carried out using a hybrid EBQQ mass spectrometer. CID spectra were obtained in two modes: B/E linked-scan mode and MS/MS mode using the EB sector combination as the first mass spectrometer and the QQ as collision cell and second mass spectrometer, respectively. Fragmentation pathways of the compounds were determined in the electron-impact mode. It was found that dominant fragmentation pathways included the loss of OH, NO2 and HNO2 in addition to the loss of CH2NNO and CH2NNO2.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 25 (1990), S. 605-608 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ionized 3-methylbutan-2-ol displays four low-energy fragmentations, loss of CH3· and C3H7· and loss of CH4 and C3H8, the latter pair being produced by metastable ion decompositions. The electron-impact, metastable-ion and collision-induced dissociation mass spectra of 13C and 2H-labelled isotopomers have been recorded, together with appearance energy measurements. It was found that the fast (ion source) losses of CH3· and C3H7· involved only simple bond cleavages between C(1) and C(2) and between C(2) and C(3), respectively, and without any positional interchange of isotopes. The loss of C3H8 produces ionized vinyl alcohol containing only C(l) and C(2). The H atoms involved are only those attached to C(1) and C(3). In deuterium-labelled analogues, the deuterium is preferentially located in the propane, e.g. metastable CD3CH(OH)CH(CH3)2 yields predominantly C3H6D2. On the basis of all the observations, it is proposed that low-energy molecular ions can form a stable proton-bridged molecule-radical complex, \documentclass{article}\pagestyle{empty}\begin{document}$ [{\rm HOCHCH}_2 \cdots \mathop {\rm H}\limits^{\rm + } \cdots \mathop {\rm C}\limits^{\rm .} {\rm H}({\rm CH}_3)_2] $\end{document}, and that this key intermediate is responsible for the isotope distribution in propane loss and also for the relatively low importance of the lowest energy dissociation, the simple C(1)—C(2) bond cleavage.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 25 (1990), S. 689-693 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Double oxygen migration to sulphur from the ortho-nitro group leading to eliminations of SO2 and ·SO2H from the molecular ions and single oxygen transfer to the olefinic double bond in the side-chain giving rise to the most abundant ion at m/z 138 have been observed in 2-nitrophenyl styryl sulphides on electron impact. The proposed fragmentation mechanisms and the product ion structures were confirmed with the aid of high-resolution data, B/E linked scan and CID spectra.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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