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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 118 (1985), S. 1668-1683 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Darstellung und einige Reaktionen von Thioacyl(diphenylthiophosphinoyl)- und Thioacyl(diphenylphosphino)sulfidenDurch Umsetzung von Natrium- oder Cäsium-dithiocarboxylaten mit Diphenylthiophosphinsäure- oder Diphenylselenophosphinsäurechloriden werden die rot-violetten Thioacyl(diphenylthiophosphinoyl)- 5 und tiefgrünen Thioacyl(diphenylselenophosphinoyl)sulfide 6, die nützliche und unter milden Reaktionsbedingungen einsetzbare Thioacylierungsmittel sind, dargestellt. Die Thioacyl-(diphenylphosphino)sulfide 22, die sich nach der gleichen Methode aus Chlor(diphenyl)-phosphan darstellen lassen, reagieren mit Methanol zu den entsprechenden Methyl-dithiocarboxylaten 15. Die Reaktionen von 22 mit N-Chlorsuccinimid liefern bisher nicht bekannte N-(Thioacylthio)succinimide 28.
    Notes: The reaction of sodium or caesium dithiocarboxylates with diphenylthiophosphinic and diphenylselenophosphinic chlorides gives purple thioacyl diphenylthiophosphinoyl 5 and dark green thioacyl diphenylselenophosphinoyl sulfides 6, which are useful thioacylating reagents under mild reaction conditions. Thioacyl diphenylphosphino sulfides 22, which can be obtained by the similar method using diphenylphosphinous chlorides, react with methanol to yield the corresponding methyl dithiocarboxylates 15, while the reactions of 22 with N-chlorosuccinimide leads to hitherto unknown N-(thioacylthio)succinimides 28.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 42 (1996), S. 1633-1641 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The graphical construction called an energy-utilization diagram (EUD) is adopted for analyses of energy transformation and exergy losses in a distillation column. The overall exergy loss on one plate of a column can be decomposed into six kinds of exergy losses and are represented graphically. Two of them are caused by mixing and cooling in the vapor phase, and the other two by mixing and heating in the liquid phase. To display the remaining two yielded by condensation and evaporation of each component, the concept of the individual energy level is applied. The relationship between the individual energy level and the xy diagram is presented as well as effects of the reflux ratio and the feed location on the EUD for the whole column. Separation of n-hexane and n-octane is used to illustrate the methodology.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 41 (1995), S. 2333-2336 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Darstellung und einige Reaktionen von unsymmetrischen Acyl(thioacyl)sulfidenDurch Umsetzung von Piperidinium- oder Natrium-dithiocarboxylaten mit Acylchloriden oder durch Entschwefelung von Acyl(thioacyl)disulfiden mit Triphenylphosphan wurden einige un-symmetrische Acyl(thioacyl)sulfide [RC(S)S(O)CR'] dargestellt und charakterisiert. Die tiefblauen Öle oder hellgrünen Kristalle sind thermisch labil und feuchtigkeitsempfindlich. Die n →π-Übergänge der Thiocarbonylgruppe in 1 treten bei höheren Wellenlängen auf als die der entsprechenden symmetrischen Bis(thioacyl)sulfide [RC(S)S(S)CR']. Einige Reaktionen mit Nucleophilen werden diskutiert. Die Umwandlung von unsymmetrischen Acyl(thioacyl)sulfiden in symmetrische Bis(thioacyl)disulfide erfolgt in Gegenwart von Basen wie Lithium-ethanthiolat mit guten Ausbeuten.
    Notes: A number of unsymmetrical acyl thioacyl sulfides [RC(S)S(O)CR'] have been prepared and characterized by the reaction of piperidinium or sodium dithiocarboxylates with acyl chlorides or by desulfurization reaction of acyl thioacyl disulfides with triphenylphosphine. They are deep blue oils or light green crystals and very unstable thermally and for moisture. The n →π transitions of the thiocarbonyl group of 1 appear in higher wave length region than those of the corresponding symmetrical bis(thioacyl) sulfides [RC(S)S(S)CR']. Some reactions with nucleophiles are discussed. It was found that the symmetricallization reaction of these unsymmetrical acyl thioacyl sulfides occurs in the presence of base such as lithium ethanethiolate to give the symmetrical bis(thioacyl) disulfides in fair yield.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 94 (1982), S. 148-149 
    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
    Angewandte Chemie International Edition in English 21 (1982), S. 150-150 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 19 (1995), S. 179-189 
    ISSN: 0308-0501
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Architecture, Civil Engineering, Surveying , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: The application of the neural networks to correlate lower and upper flammability limits with chemical structures or basic physical properties for 150 organic compounds of diverse structures and functionalities was investigated. The prediction results based on a three-layer neural network with a back-propagation algorithm were compared with those obtained by multiple regression analysis. The comparison showed showed that the neural networks gave better versatility (range of applicability) and reliability. The predictive ability of the methods developed were tested for a new set of 50 compounds not included in the training data set and good agreement with observed lower and upper flammability limits was confirmed. The required information for the calculation were six easily available properties: standard enthalpy of combustion, molecular weight, critical temperature, critical pressure, oxygen balance, and diffusion coefficient in air. By using these calculable properties from the molecular structure, the method could be used to predict flammability limits of new compounds containing C, H, O, N, S, Cl, F and Br atoms.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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