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  • 1
    Electronic Resource
    Electronic Resource
    Scaling and performance of CO2 lasers at supra-atmospheric pressure (1985)
    Springer
    Applied physics 37 (1985), S. 171-179 
    Details
    ISSN: 1432-0649
    Keywords: 42.55D ; 42.60B ; 58.80
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The performance of a compact uv photo-preionized TE laser is studied in the pressure range 1–5 bar. As the pressure is increased, the laser pulse shape is little altered, but both the peak power and the total output pulse energy increase significantly with pressure, even for constant input electrical energy. For various gas mixtures and excitation source capacitors the measurements suggest approximate output energy scaling with the product of the source charge per unit electrode area [C.m−2] and the molecular partial pressure [CO2+N2+CO]. This is explained in terms of the pressure-dependent discharge impedance. An input-energy-related discharge instability limits the optimum laser pressure to 1.5–2.5 bar, and we show that, at constant input energy, the instability boundary depends on the molecular partial pressure alone. The pre-ionization photo-electron yield varies negligibly with pressure, but the discharge tolerance to added oxygen decreases asp −3 top −4, dependent on gas mixture. Nevertheless sealed operation for 〉105 shots has been obtained with a 5% CO2∶5% CO∶3% N2∶2% H2∶85% He gas mixture at a total pressure of 5 bar.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00692081
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  • 2
    Electronic Resource
    Electronic Resource
    X-ray preionized CO2 laser (1985)
    Springer
    Applied physics 37 (1985), S. 219-221 
    Details
    ISSN: 1432-0649
    Keywords: 42.55D ; 33.80E ; 52.80 ; 42.60B
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A short pulse (100 ns) high-energy x-ray source has been used to preionize a transversely excited carbon dioxide gas discharge laser of 600 cm3 active volume. The maximum output power of 60 MW in a 50 ns FWHM pulse was achieved from a CO2−N2−He−CO−Xe static gas mixture at 600 Torr pressure. The energy conversion efficiency was 6%.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00692945
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  • 3
    Electronic Resource
    Electronic Resource
    Effective and simplified hybrid TEA laser design and operation (1984)
    Springer
    Applied physics 33 (1984), S. 99-101 
    Details
    ISSN: 1432-0649
    Keywords: 42.60B ; 42.55D
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A compact hybrid TEA CO2 laser has been developed which, when operated with the low pressure section well below oscillation threshold, demonstrates that little cw gain is necessary to ensure single longitudinal mode (SLM) output pulses with peak power, energy and pulse shape approaching those of normal multi-mode operation. This has allowed reliable SLM operation to be obtained with a very short, wide bore rf-excited low-pressure section, making feasible simple single-mode, large-aperture TEA lasers with high peak powers and energies.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00688354
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  • 4
    Electronic Resource
    Electronic Resource
    Über einige β-Dialkylaminobuttersäureamide mit anästhetischer Wirkung (1953)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 36 (1953), S. 1698-1705 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of some β-alkylaminobutyric-acid-amides from the corresponding crotonic acid amides and dimethyl or diethylamine under pressure at 100-150° is described. Two diethylamino acetic acid amides were prepared by reacting N-benzyl-chloracetamide or N-(pethoxybenzyl)-chloracetamide with diethylamine. All these β-dialkyl-aminobutyric and dialkylaminoacetic acid amides show local anaesthetic activity. Two of them (β-diethylaminobutyric acid anilide and β-diethylamino-butyric acid-p-phenetidide) show promise as long acting anaesthetics of low toxicity for nerve block anaesthesia, and are under clinical investigation.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19530360703
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  • 5
    Electronic Resource
    Electronic Resource
    Influence des substituants sur la vitesse de racémisation des cétones à carbone dissymétrique en alpha (1960)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 1915-1927 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rates of racemisation, under constant conditions of pH and temperature, of two series of ketones with an asymmetric C-atom in α have been determined. As would be expected, substituents in the α position to the keto group influence the rate of racemisation, and it has been found possible to assess the relative electron donating or electron attracting effect of aliphatic, aliphatic-aromatic or aromatic substituents by measuring their influence on the rate of racemisation of a ketone containing the substituent considered.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19600430705
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  • 6
    Electronic Resource
    Electronic Resource
    Über die Herstellung und physiologischen Eigenschaften einiger Acetylenverbindungen und verwandter Stoffe. 2. Mitteilung. Über die Umlagerung von 3,4-Di-p-anisyl-3-ol-hexin-(1) (1953)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 36 (1953), S. 1949-1955 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Attempts to remove water from 3,4-di-p-anisyl-1-hexyn-3-ol in acid medium resulted in rearrangement according to Meyer-Schuster principally and to Rupe to a minor extent. None of the derivatives of these rearrangement products reached the oestrogenicity of stilboestrol. The dehydration of 3,4-di-p-anisyl-3-hexen-2-ol does not lead to the expected diene but to the corresponding methylether of the known 1-ethyl-2-p-hydroxyphenyl-3-methyl-5-hydroxyindene.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19530360734
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  • 7
    Electronic Resource
    Electronic Resource
    Über einige β-substituierte Fettsäureamide mit lokalanästhetischer Wirkung (1955)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 38 (1955), S. 1085-1095 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation and properties of further fatty acid anilides showing anaesthetic action are described and the relationship between chemical constitution and physiological effect is discussed. Two very active compounds having relatively low toxicities have been discovered, namely:-β-piperidino-n-butyric-acid-2,4-dichloranilide (XIV) and β-(2-methylpiperidino)-n-butyric-acid-anilide (V). A number of similar anilides show high activities, but other undesirable properties such as tissue irritation render them less useful.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19550380502
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  • 8
    Electronic Resource
    Electronic Resource
    Über einige β-substituierte Fettsäureamide mit lokalanästhetischer Wirkung. 4. Mitteilung (1959)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 42 (1959), S. 1764-1771 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation and properties of some new β-alkylamino-butyric anilides have been described and a summary report on some of their pharmacological properties is given. Two derivatives (the p-(carbo-n-butoxy)-anilides of β-diethylamino- and of β-(1-piperidino)- butyric acid = XVI and XVIII) show promise as very active local anaesthetics with low toxicities. One derivative (β-N-pyrrolidino-n-butyric acid anilide = XXVII) shows strong potentiation of the sedative properties of barbiturates.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19590420603
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  • 9
    Electronic Resource
    Electronic Resource
    Über einige β-substituierte Fettsäureamide mit lokalanästhetischer Wirkung. 5. Mitteilung (1959)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 42 (1959), S. 1771-1779 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A further series of butyric acid amides has been synthesised in which the diethylamino, pyrrolidino and piperidino groups of previously reported syntheses have been substituted by morpholino groups. The influence of the various groups in the present and in previously reported derivatives on the pharmacology of the series is reported and summarised. The conditions necessary for maximum local anaesthesia and barbiturate potentiation are discussed.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19590420604
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  • 10
    Electronic Resource
    Electronic Resource
    Über die Herstellung und physiologischen Eigenschaften einiger Acetylenverbindungen und verwandter Stoffe. 1. Mitteilung (1953)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 36 (1953), S. 1706-1710 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of 3-p-methoxyphenyl-1-pentyne-3-ol,3-p-methoxyphenyl-2-pentene-4-yne, 3,4-bis(p-methoxyphenyl)-1-hexyne-3-ol, some reaction products and the physiological properties of these substances are described. 3,4-Bis(p-methoxyphenyl)-hexyne-ol is practically non-toxic and possesses sedative properties.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19530360704
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