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  • 1970-1974  (7)
  • Analytical Chemistry and Spectroscopy  (6)
  • Cat tongue  (1)
  • Organic Chemistry
  • 1
    ISSN: 1432-1106
    Keywords: Geniculate ganglion ; Facial nerve ; Cat sensory systems ; Taste ; Tongue chemoreceptors ; Fungiform papillae ; Cat tongue
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Within the cat geniculate ganglion three distinct neural populations were definable on the basis of single unit recordings. These three neural populations were designated “ear units”, “regular discharge units” and “tongue units.” Units from these three populations tended to be located in different regions of the ganglion and were influenced by different types of stimulation to different parts of the body. 2. Ear units seemed to constitute a uniform functional population, with the major differences between units being the external locus of projection. Ear units typically had no spontaneous activity. They were discharged by dynamic displacements of hairs on the skin of the inner surface of the ear. 3. Regular discharge units were classified into three types on the basis of their spontaneous activity patterns. Discharge of most of the units could be affected by static dislocations of tissues of the soft palate and pharynx. Discharge patterns, evoked and spontaneous, tended to be extremely regular. 4. Tongue units seemed to constitute an extremely diverse population. Wide variability was shown on every measure taken of tongue unit activity. Spontaneous activity patterns varied markedly from unit to unit, with bursting discharge common. Most units could be discharged by electrical stimulation of papillae of the tongue, although the number of stimulatable papillae varied from unit to unit as did latency measures. Some tongue units were discharged by mechanical stimulation of the tongue, most by chemical stimulation of the tongue (with salt, acid, quinine and common cat foods), and some by both.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 1055-1066 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron-impact mass spectra and the field ionization mass spectra of 1-chloro-2-nitrosocyclohexane and 1-chloro-2-nitrosocyclopetane are presented and discussed. The two compounds investigated exist in dimeric form in the gaseous phase.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 4 (1970), S. 503-512 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Five phenarsazine derivatives with arsenic in the trivalent state and the pentavalent state are studied by mass spectrometry. Their characteristic fragmentation modes and the fragment ions with common structures are discussed. Experimental results show that the pyrolytic decompositions of the phenarsazine derivatives are closely parallel to the unimolecular ion fragmentation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 287-302 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nine phenoxarsine derivatives with arsenic in the trivalent state and the pentavalent state are synthesized and studied by mass spectrometry. Their characteristic fragmentation modes and the fragment ions with common structures are discussed. Phenoxarsinic acids are found to be unstable in the gaseous phase at the temperatures studied and tend to form their corresponding anhydrides.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 833-841 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The EI Mass spectra of the polyfunctional pentaerythritol derivatives show that the molecular ions [M]+· exhibit extensive ion fragmentation. No Information about [M]+·. can be obtained. In Contrast to this, the FI Mass spectra of these compounds show intense [M]+· and/or [M + 1]+, and a characteristic ion at m/e 31, which is assumed to be the oxonium ion \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_2 = \mathop {\rm O}\limits^ + {\rm H} $\end{document}. Because of surface adsorption and field attraction, FI mass spectrometry presents a serious problem in quantitative analysis of a mixture containing compounds with quite different degrees of polarization.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 747-751 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The predicted pyrolyzate of phenoxarsine derivatives from their mass spectra is diphenylene oxide. The prediction is verified by the experiment.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 493-500 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermally and electron-impact-induced rearrangements of the dimethylthioncarbamates to the dimethylthiolcarbamates are discussed. Owing to the competition with the ion fragmentation reactions in the mass spectrometric time, 〈 10-6 seconds, the extent of the mass spectrometrically observed ion isomerization cannot be predicted from that of the thermal induced one. In the ion fragmentations of the non-rearranged molecular ions, it was found that the relative abundance of the ion (CH3)2NC≡O⊕ to the total ionization is larger than that of the ion (CH3)2NC≡S⊕. This is believed to be attributable to the differences in the dissociation energies of the C—S bond and the C—O bond and in the stabilities of the two ions.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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