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  • 1985-1989  (4)
  • 1975-1979  (1)
  • Organic Chemistry  (4)
  • 27.20.+n  (1)
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Year
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  • 1
    Electronic Resource
    Electronic Resource
    Line shape and excitation strength of the first excited state in9Be (1987)
    Springer
    The European physical journal 326 (1987), S. 447-454 
    Details
    ISSN: 1434-601X
    Keywords: 21.60.CS ; 25.30.Dh ; 27.20.+n
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The line shape and the excitation strength of the very weak first excited J π =1/2+ state at Ex=1.684 MeV in Zeitschrift für Physik Zeitschrift für Physik9Be has been investigated with high-resolution inelastic electron scattering at E0=45 and 49 MeV and scattering angles θ=105°, 117°, 129° and 165°, and with high-resolution inelastic proton scattering at E0=13MeV and θ=15° and 18°. Due to lying just above the neutron threshold the level has a strongly asymmetric line shape which in both experiments can be described consistently with a Breit-Wigner expression modified on the low energy side by the threshold behaviour of the cross section. The resonance energy is ER=1.684 ± 0.007 MeV and the width T=217± 10 keV in thec.m. system. A single particle potential model calculation reproduces the line shape and the resonance parameters fairly well. In addition, the inelastic electron scattering form factor has been measured. In the range of momentum transfersq =0.24-0.46 fm−1 it is dominated by a 0p3/2→ 1s1/2 particle-hole transition. The transition is mainly longitudinal and of isoscalar nature with a strength of B (E1)↑ =0.027 + 0.002 e2 fm2, but a small M2 contribution ofB(M2)↑=8.8 ±1.5 μ N 2 fm2 has also been detected.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01289549
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Organische Elektronenleiter und Vorstufen. V.IV. Mitt.: RICHTER, A. M.; FANGHÄNEL E.: Sulfur Lett. 3 (1985) 25. Synthese von Poly(organylthio-acetylenen) (1987)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 329 (1987), S. 811-816 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Electron Conductors and Precursors. V. Synthesis of Poly (organylthio-acetylenes)Poly(bis-organylthio-acetylenes) 2 and poly(mono-organylthio-acetylenes) 3 have been synthesized by complex catalyzed polymerization of the corresponding acetylenes (4 resp. 5). Yields and properties of the polymers 2, 3 depend on reaction conditions, the catalyst and the nature of the acetylenes. Relations between these influence factors are discussed.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19873290509
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Iodierung von N-Aryl-2,4-dimethyl-buta-1,3-dien-1,4-sultamen (1985)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 428-432 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Iodation of N-Aryl-2,4-dimethyl-buta-1,3-dien-1,4-sultamesBy the iodation of N-aryl-2,4-dimethyl-buta-1,3-dien-1,4-sultames 1 with I2/HgO in EtOH/AcOH the 1,2-thiazine ring is substituted. The monosubstitution occurs on the 1-position (1a, d) and the disubstitution on the 1,3-position (3a). By iodine monochloride in CHCl3 the sultames 1a-d were substituted in the (C-2)-CH3 group (4a-d), in contrast also to the results of chlorination and bromination of 1. The structure of the products 2, 3, 4 was proved by 13C-n.m.r. spectroscopic data.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19853270309
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Synthese von 2-Heterocyclidenamino-1,3-diazatrimethincyaninen (1979)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 321 (1979), S. 827-834 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of 2-Heterocyclidenamino-1, 3-diaza-trimethincyaninesThe synthesis of 2-[3-methyl-benzthiazol-(1, 3)-inylidene-(2)-amino]- and of substituted 2-[1, 3-dithiolyliden-(2)-amino]-1, 3-diaza-trimethincyanines is described. The heterocyclic imines 1 react with phosgene or thiophosgene to the corresponding ureas 2 and thiureas 3, respectively. Alkylation of 3 to the 2-alkylmercapto-1, 3-diaza-trimethincyanines 4 and subsequent condensation with imine 1 yields the dyes 5. The chemical and spectroscopical data of cyanines 5 are described.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19793210514
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  • 5
    Electronic Resource
    Electronic Resource
    Heterocyclisch substitutierte Arendiazoniumsalze mit erweiterter spektraler Empfindlichkeit - Teil I: Monomethine und AzamethineHerrn Professor Dr. E. Schmitz zum 60. Geburtstag gewidmet (1988)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 330 (1988), S. 590-606 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Heterocyclic Substituted Arendiazonium Salts with a Long-wave-length Range of Sensitivity  -  Part I: Monomethins and AzamethinsTwo new types of arendiazonium salts have been synthesized. In these compounds a heterocycliden ring is bridged through a methine group (8a-o) or a nitrogen (11a-c) with the 4-position of a benzene diazonium group.Both types show sensitivity towards normal day-light, their long wave-length absorption band vary from 430 nm up to 590 nm, depending on the donor strength of the heterocycliden ring and the nature of the bridging group.The thermostability, the quantum yields of photochemical dediazonation and the coupling behaviour of the diazonium salts are investigated, in order to evaluate their potential applicability in a commercial diazotype system.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19883300413
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