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  • Inorganic Chemistry  (6)
  • General Chemistry  (4)
  • Organic Chemistry  (2)
  • Atomic and molecular structure and dynamics  (1)
  • Surface physics, nanoscale physics, low-dimensional systems
  • 2010-2014  (2)
  • 1985-1989  (4)
  • 1960-1964  (8)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 2209-2209 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 459-464 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Substituted 3,4-Diamino-thieno[2,3-b]pyrroles
    Additional Material: 2 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 76 (1964), S. 615-615 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 330 (1988), S. 735-747 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photochemistry and Photophysics of 3-(2-Isoxazolinyl)-phenylketones3-Benzoyl-Δ2-1,2-oxazolines (1-6) are formed by 1,3-dipolar cycloaddition between benzoylnitril-N-oxide (8) and dihydrofurane 9 or 1,3-dioxep-5-enes (10a-c). The preparative yields are small due to the competitive dimerization of the dipole 8. Two stereoisomers are obtained by using 2-substituted 1,3-dioxep-5-enes as dipolarophiles. The different steric position of the substituents in 3-6 gives rise to different spectral data. The synthesized ketones possess triplet states with a high degree of charge transfer character. Therefore, the ability to H-abstraction reaction from alcohols is small. For ketone 2 and methanol as H-donor a rate constant of kHMeOH = 4,1 · 102 M-1s-1 is determined. Also by electron transfer reactions with triethylamine and some onium compounds the reactivity of the T1 of the ketones 1-6 is less compared to those of nπ* excited ketones. The photolysis of the ketones takes place very unselectively and leads to a product mixture. The quantum yields for the decay of the ketones are 10-2 to 10-3.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 553 (1987), S. 239-247 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of elemental Sulfur with Halogenated MethanesAt 250°C a reaction between CCl4 and sulfur forms S2Cl2 and CS2 (besides small amounts of S3Cl2 and S4Cl2). CHCl3 and sulfur above 200°C under catalytic influence of AlCl3 are forming HCl, S2Cl2, and CS2; CH2Cl2 and sulfur also are reacting (with AlCl3 or AI as catalyst) to CS2 and HCl. Only at 345°C one gets,CS2, HCl, and H2S from CH3Cl and sulfur. At 160°C forms HBR,BR2, and CS2. Aluminium is necessary for the reaction of CH2Br2 at 250°C with sulfur, forming CS2 and HBr. A mixture of products (CS2,H2S, HBr, CH3SCH3, and (CH3)3SBr) results from CH3 Br and sulfur at 250°C. CH3I and sulfur produce CS2,I2, and H2S at 145°C. The same products are formed from CH2I2 and sulfur with aluminium as catalyst at 175°C.
    Notes: CCl4 reagiert bei 250°C mit Schwefel zu S2Cl2 und CS2 (neben wenig S3Cl2 und S4Cl2). Aus CHCl3 und Schwefel bilden sich oberhalb 200°C unter AlCl3-Katalyse HCl, S2Cl2 und Cs2. CH2Cl2 und Schwefel liefern (wieder mit AlCl3 bzw. auch Al) CS2 und HCl. CH3Cl reagiert mit Schwefel erst oberhalb 345°C zu CS2, HCl und H2S. CBr4erst ab 245°C mit Schwefel zu HBR, Br2un 1 CS2 umsetzt. CH2BR2 benötigt bei 250°C wieder Aluminium als Katalysator, um mit Schwefel CS2 und HBr zu bilden. CH3Br reagiert mit Schwefel bei 250° zu einem nicht genau definierten Produktgemisch aus CS2, H2S, HBr, Ch3SCH3 und (CH3)3 SBr. Aus CHI3 und Schwefel erhält man bei 145°C CS2,i2 undH2S, ebenso wie aus CH2I2 und Schwefel, allerdings nur unter Aluminiumkatalyse bei 175°C.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 1 (1962), S. 327-328 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 1 (1962), S. 661-661 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 1 (1962), S. 660-660 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 330 (1964), S. 130-140 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The reaction of hydrogen sulfide with sulfuryl chloride in the ratio 2:1 leads in benzene solution to hydrogen chloride, water, sulfur, and disulfur monoxide, S2O, which is surprisingly stable under the prevailing conditions. The reaction of sulfuryl chloride with liquid hydrogen sulfide leads to the formation of sulfanes and chlorosulfanes, respectively, besides other products, depending on the molar ratio H2S:SO2Cl2.
    Notes: Schwefelwasserstoff reagiert mit Sulfurylchlorid beim molaren Einsatz 2:1 in benzolischer Lösung unter Bildung von Chlorwasserstoff, Wasser, Schwefel und Dischwefelmonoxid S2O, das unter den herrschenden Reaktionsbedingungen überraschend stabil ist. Mit flüssigem Schwefelwasserstoff bildet SO2Cl2 im Unterschuß u. a. Sulfane, im Überschuß Chlorsulfane.
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 330 (1964), S. 188-194 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The separation of sulfane-disulfonates, sulfite and thiosulfate by anion-exchangers has been studied. Whereas K2S6O6 is decomposed on the column, the salts K2S3O6, K2S4O6 and K2S5O6 may be separated quantitatively.
    Notes: Die Trennung von Sulfan-disulfonaten, Sulfit und Thiosulfat mit Anionenaustauschern wird untersucht. Während K2S6O6 auf der Säule zu rasch zerfällt, lassen sich die Salze K2S3O6, K2S4O6 und K2S5O6 quantitativ voneinander trennen.
    Additional Material: 1 Ill.
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