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  • Chemistry  (24)
  • Normal Coordinate Analysis  (2)
  • Wiley-Blackwell  (24)
  • Oxford University Press
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 92 (1959), S. 1105-1112 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es werden 2-[p-Aminosulfonyl-phenylhydrazino]-thiazole beschrieben, die durch Kondensation von 1-[p-Aminosulfonyl-phenyl]-thiosemicarbazid mit α-Halogen-carbonylverbindungen in äthanol. Lösung zugänglich sind. Führt man die gleichen Umsetzungen mit Chloraceton bzw. ω-Chlor-acetophenon in konz. Salzsäure durch, so entsteht das 3-[p-Aminosulfonyl-anilino]-4-methyl-thiazolon-(2)-imid bzw. das 2-Amino-4-[p-aminosulfonyl-phenyl]-5-phenyl-1.3.4-thiodiazin. Ersteres sowie das 3-[p-Aminosulfonyl-anilino]-4.5-dimethyl-thiazolon-(2)-imid lassen sich auch aus Rhodanaceton bzw. 3-Rhodan-butanon-(2) und p-Aminosulfonyl-phenylhydrazin-hydrochlorid darstellen. Dagegen erhält man aus ω-Rhodan-acetophenon und p-Aminosulfonyl-phenylhydrazin-hydrochlorid das Phenylglyoxal-bis-[p-aminosulfonyl-phenylhydrazon].
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 118 (1985), S. 888-894 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Transition Metal Fulvene Complexes, XXIII. Tricarbonyl Fulvene and Tricarbonyl Cyclopentadienyl Complexes of Molybdenum and TungstenIn contrast to the reaction of fulvenes with (CH3CN)3Cr(CO)3, which leads to pure (fulvene)Cr- (CO)3 complexes, the reaction of L3M(CO)3 [L3 = 3 CH3CN, diglyme; M = Mo, W] with fulvenes gives a mixture of (fulvene)M(CO)3 (2) and substituted dimeric (cyclopentadienyl)2M2-(CO)6 complexes (3) difficult to separate. The structure of bis(η5-benzhydrylcyclopentadienyl)- hexacarbonyldimolybdenum (3a) has been determined by X-ray diffraction. The (fulvene)Mo-(CO)3 complex 4 reacts with tertiary phosphanes and methylenetriphenylphosphorane to give the zwitterionic addition products 5 and 6.
    Notes: Im Gegensatz zu Reaktion von Fulvenen mit (CH3CN)3Cr(CO)3, die zu reinen (Fulven)Cr-(CO)3-Komplexen führen, gibt die Umsetzung von L3M(CO)3 [L3 = 3 CH3CN, diglyme; M = Mo, W] mit Fulvenen eine Mischung aus (Fulven)M(CO)3 (2) und substituierten dimeren (Cyclopentadienyl)2M2(CO)6-Komplexen (3), die schwierig zu trennen ist. Die Struktur des Bis(η5-benzhydrylcyclopentadienyl)hexacarbonyldimolybdäns (3a) wurde röntgenographisch bestimmt. Der (Fulven)Mo(CO)3-Komplex 4 reagiert mit tertiären Phosphanen und Methylentriphenylphosphoran zu den zwitterionischen Additionsprodukten 5 und 6.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 32 (1998), S. VI 
    ISSN: 0009-2851
    Keywords: Chemistry ; 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
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 54 (1941), S. 328-328 
    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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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 72 (1960), S. 493-493 
    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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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 77 (1965), S. 172-172 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
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  • 7
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effects of gamma irradiation in four types of irradiation environment on the thermal and tensile properties of gel-spun, ultrahigh molecular weight polyethylene fibers (Spectra™ 1000) have been investigated. The gamma irradiation was conducted at 2.5 Mrad and in air, nitrogen, acetylene, and vacuum to study the effects of irradiation media on the aforementioned properties. Thermal and tensile properties of virgin and irradiated fiber samples were examined using differential scanning calorimetry and an Instron tensile tester, respectively. The results indicate that both gamma irradiation and irradiation environment affected the properties of the polyethylene fibers, and substantial changes were observed for the oxygen-containing environment. The tensile-fractured surfaces of the fibers were examined by scanning electron microscopy. The properties of irradiated fibers were further evaluated at 160 days postirradiation and found to be affected, substantially. The postirradiation aging significantly decreased the tensile strength and elongation of the irradiated fibers, indicating that polyethylene fibers should not be exposed to gamma irradiation. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 8
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Several N-(phosphonomethyl) amides have previously been reported to act as particularly effective flame retardants for cellulose. It has also been demonstrated previously that the efficiency of a flame retardant on cellulose frequently parallels its ability to phosphorylate cellulosic hydroxyls at elevated temperatures. This study of the hydrolysis and alcoholysis reactions of N-(phosphonomethyl) amides establishes their unique reactivity. An explanation for this high reactivity is proposed on the basis of intramolecular assistance of the attack of water or alcohols at phosphorus by the carbonyl oxygen of the amide moiety.
    Additional Material: 6 Ill.
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  • 9
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An investigation of the thermal decomposition of N-dimethylphosphonomethyl amides has shown that the major volatile products for decomposition above 300°C are methanol, the methyl ester of the carboxylic acid, the nitrile, the carboxylic acid, the N-methyl amide, and the N,N-dimethyl amide. Also, benzoic acid was the only volatile product detected in the decomposition of α-benzamidomethylphosphonic acid. A mass balance for the decomposition of N-dimethylphosphonomethyl benzamide at 420°C showed methanol and methyl benzoate to be the major volatile products. Methanol and benzonitrile formation increased with an increase in temperature at a faster rate than the other volatile products. The reaction of amides and phosphonates was further studied using sealed tubes in a furnace. Reaction of N-methylbenzamide with dimethyl methylphosphonate at 307°C in a sealed tube produced methyl benzoate and N,N-dimethylbenzamide. N,N-dimethylbenzamide and dimethylmethylphosphonate were also shown to produce methyl benzoate at 310°C. After a 5-min period more methyl benzoate was produced in the N,N-dimethylbenzamide reaction than in the N-methylbenzamide reaction. Also, addition of ethanol to the N,N-dimethylbenzamide/dimethyl methylphosphonate reaction resulted in less ethyl benzoate methyl benzoate after heating at 310°C.
    Additional Material: 4 Ill.
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  • 10
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Thermal gravimetric analysis, differential scanning calorimetry, and derivative thermal gravimetric analysis were utilized to characterize the thermal interactions between cellulose, 1-6, anhydro β-D-glucopyranoside, and D-glucose and model phosphate and phosphoramide flame retardants. The phosphoramides induced higher char yields than the phosphates during the pyrolysis of the mixtures of carbohydrates and organophosphorus compounds. Exothermic reactions attributed to phosphorylation and char formation were observed with each of the phosphoramide/carbohydrate mixtures and were absent with the phosphates. The individual phosphorus compounds studied showed similar thermal behavior with each of the carbohydrates indicating that the mode of interaction for these mixtures was similar. Isothermal gravimetric analysis of the organophosphorus/carbohydrate mixtures was used to measure the rate of decomposition weight loss from isothermal conditions. This weight loss was used as an indication of rate of fuel formation. The kinetics observed for these measurements indicated that the phosphoramide mixtures underwent a rapid weight loss to a final char with an effective Eact of about 55 kcal/mol while the phosphate mixtures exhibited effective Eact′s for decomposition lower than those observed for the pure carbohydrates. Mixtures of glucose with selcted arylphosphoramide esters were pyrolysed in order to determine the effect of lability of the leaving group on char formation. Gas chromatographic analysis of the pyrolysis products indicated that phenol was the favored leaving group in comparison with aniline units, but char promotion appeared to be dependent on the number of P-N bonds present in the original phosphoramide. Electron spectroscopy for chemical analysis indicated that chemically similar chars were obtained from the different organophosphorus/carbohydrate combinations.
    Additional Material: 14 Ill.
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