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  • Chemistry  (91)
  • 61.70  (3)
  • 78.70  (2)
  • 2-Arylhydrazono-2-cyan-N-chloracetylacetamide  (1)
  • Wiley-Blackwell  (91)
  • Springer  (4)
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  • Wiley-Blackwell  (91)
  • Springer  (4)
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Monatshefte für Chemie 122 (1991), S. 195-207 
    ISSN: 1434-4475
    Schlagwort(e): 5-Dialkylamino-2-aryl-1,2,3-triazoles ; 4-Amino-2,6-dioxo-tetrahydropyrid-3-yl-pyridiniumchloride ; 2-Arylhydrazono-2-cyan-N-chloracetylacetamide ; Arylhydrazono-2-cyan-N,N-dialkylacetamidines ; Arylhydrazonomalononitriles ; 4-Imino-5-arylazo-6-dialkylamino-1,4-dihydropyrimidines ; 13C-NMR
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Summary The title compounds3 were synthesized by reaction of arlyhydrazono-malononitriles1 with secondary amines and used for subsequent cyclization reactions. Thus,3 undergoes cyclooxidation by treatment with CuSO4/pyridine to form the 5-dialkylamino-2-aryl-1,2,3-triazolo-4-carbonitriles4. From4 a and hydrazine hydrate/DMF the 4-(1,3,4-triazolyl-5)-1,2,3-triazole5 c is obtainable. The chloroacetylation of3 is accompanied by hydrolysis of the amino group to yield the arylhydrazono-N-chloracetyl cyanoacetamides6. The quaternisation of6 with pyridins is followed by the Thorpe cyclization to form the 4-amino-5-arylazo-6-hydroxy-3-pyridinio-pyrid-2-on-chlorides8, useful as cationic dyes. The reaction of3 with trichloroacetonitriles yields the 5-arylazo-4-imino-2-trichlormethyl-1,4-dihydropyrimidines10 a–c which can be converted into the 5-arylazo-2-hydrazino-pyrimidine derivatives10 d–f. From10 d the 6-phenylazo-triazolo[4,3-a]pyrimidine derivative11 is obtainable. From3 and phenylisothiocyanate the 5-arylazo-4-imino-1,4-dihydropyrimidin-2-thiones12 arise. The structures were investigated by13C-NMR-spectroscopy.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Applied physics 61 (1995), S. 51-53 
    ISSN: 1432-0630
    Schlagwort(e): 61.70 ; 61.80 ; 78.70
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Maschinenbau , Physik
    Notizen: Abstract The present paper reports on positron lifetime measurements on atomic defects in SiC after low-temperature (80 K) electron irradiation of low (0.47 MeV) and high (2.5 MeV) electron energies and doses from 1.8×1017 to 1.9×1019 e/cm2 as well as after subsequent isochronal annealing up to 1900 K. For these studies the single crystals of nitrogen doped (2–3×1018 cm−3) SiC grown by a modified Lely technique with hexagonal structure (6H polytype) were used. According to the positron lifetime measurements, very different types of vacancy-like positron traps are introducted after irradiation with electrons of either low or high energy. The formation of defect agglomerates and their decay at high temperatures is studied during isochronal annealing and related to earlier studies.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 1432-0630
    Schlagwort(e): 61.70 ; 81
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Maschinenbau , Physik
    Notizen: Abstract By means of an integrated source-specimen technique the temperature dependence of positron lifetimes and annihilation lineshapes has been measured, on the same specimens of gold and cadmium from 4.2K to the melting points, and also in electronirradiated and quenched gold. The anomalous temperature dependence of positron annihilation at intermediate temperatures (200 to 350 K in Cd, 270 to 750 K in Au) discovered by Lichtenberger, Schulte, and MacKenzie is confirmed. The data are incompatible with the idea that the intermediate temperature dependence is due to thermal expansion. They are well explained by an extension of the trapping model which includes the formation of metastable self-trapped positrons. From lineshape measurements after electron irradiation at 180 K and after quenching it is deduced that the trapping rate of positrons at vacancy-type defects in Au is temperature independent below room temperature.
    Materialart: Digitale Medien
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  • 4
    ISSN: 1432-0630
    Schlagwort(e): 78.70 ; 61.70 ; 07.77
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Maschinenbau , Physik
    Notizen: Abstract A slow-positron source has been installed in the therminal of an electrostatic 6.5 MeV accelerator and provides a monoenergetic positron beam in the few-MeV range. It will be used to operate a “fast” positron lifetime spectrometer based onβ + γ coincidences. The properties of the beam, the expected performance of the spectrometer, its advantages over conventionalγγ lifetime measurements, a number of intended applications, as well as recent positron-electron scattering experiments and plans for positron channelling and channelling-radiation studies are outlined.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 149-158 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Cyclizations with 1-nitro-2-anilino-ethylenesThe reaction of 1-nitro-2-anilino-2-methylthio-ethylenes 1 with oxalyl chloride yields the substituted 4-nitropyrrol-2,3-diones 4, and with chlorocarbonyl-sulfenylchloride the 5-nitro-thiazolones 6. The methylthio group from 6 can be exchanged by amines. From 1-nitro-2,2-bis(anilino)ethylenes 2 - available from 1-nitro-2,2-bis(methylthio)-ethylene and anilines - and the same reagents, the substituted 2-nitromethylene-imidazolidine-4,5-diones 5 and the thiazolo[4,5-d]thiazoledione 9 result. The condensation of 1-nitro-2-anilino-2-hydrazino-ethylene 3 with derivatives of carboxylic acids yields 2-nitromethyl-s-triazole 12, with diacetyl the substituted 3-nitromethylene-as-triazine 13.
    Notizen: 1-Nitro-2-anilino-2-methylmercapto-äthylen 1 reagiert mit Oxalylchlorid zu substituierten 4-Nitropyrroldionen-(2,3) 4 und mit Chlorcarbonyl-sulfenylchlorid zu substituierten 5-Nitrothiazolonen-(2) 6, deren Methylmercaptogruppe gegen Amine austauschbar ist. 1-Nitro-2,2-bis(anilino)-äthylene 2 - erhältlich aus 1-Nitro-2,2-bis(methylmercapto)-äthylen und Anilinen  -  liefert mit den gleichen Agenzien substituierte 2-Nitromethylenimidazolidindione-(4,5) 5 und das Thiazolo[4,5-d]thiazoldion 9. 1-Nitro-2-anilino-2-hydrazino-äthylen 3 wird mit Carbonsäurederivaten zu substituierten 2-Nitromethyl-s-triazolen 12, mit Diacetyl zum 3-Nitromethylen-as-triazin derivat 13 kondensiert.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 323 (1981), S. 133-136 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Methyl(3-amino-5-nitromethylene-1,2-dithiol-4)carboxylate
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 329 (1987), S. 745-748 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 329 (1987), S. 355-358 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 5-Arylamino-3-bromo-1,2,4-thiadiazoles and 5-Arylamino-3-bromo-isothiazoles
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 933-941 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Reaction of Methylene Active Nitriles and Cyanamide with Acylated EnaminesThe addition products from enamines onto isocyanates and isothiocyanates, i.e. substituted β-aminoacrylo amides 1 and thioamides 2, react with malononitrile to yield the 6-amino-1-aryl-5-cyano-pyridin-2-ones 3 and -thiones 4 among them 5,6,7,8-tetrahydroisoquinolin-1-ones and -thiones. From ethyl cyanoacetate the 5-cyano-6-hydroxy-pyridin-2-ones 7 and from benzoyl acetonitrile the 6-phenyl-pyridin-2-ones 8 are formed. The replacement of malononitrile by cyanamide yields the 2-amino-3-aryl-pyrimidin-4-ones 5 and -thiones 6 among them 5,6,7,8-tetrahydroquinazolin-4-ones and -thiones. The not isolated β-acyl enamines derived from enamines and acid chlorides react with malononitrile or cyanamide to form the pyridin-2-ones 14 or pyrimidin-2-ones 15 caused by Dimroth-rearrangement.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 328-332 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Reaction of 1, 1-Dimethylthio- and 1-Dimethylamino-2-nitroethene with Malononitrile Dimer
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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