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  • Wiley-Blackwell  (17)
  • 1985-1989  (7)
  • 1975-1979  (10)
  • 1935-1939
  • 1930-1934
  • 1
    Electronic Resource
    Electronic Resource
    Cycloaddition von Benzothiet an 4-substituierte Styrole (1989)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 2209-2209 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19891221125
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  • 2
    Electronic Resource
    Electronic Resource
    Substituierte 3,4-Diamino-thieno[2,3-b]pyrrole (1986)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 459-464 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19863280325
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  • 3
    Electronic Resource
    Electronic Resource
    Suspension polymerization of vinyl chloride. I. Influence of viscosity of suspension medium on resin properties (1989)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 37 (1989), S. 145-166 
    Details
    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 suspension polymerization of vinyl chloride is studied in a bench-scale reactor adequately reproducing reaction conditions and resin properties of industrial relevance. The evolution of particle morphology is analyzed at different stages of conversion, and a model for particle formation is verified. The influence of viscosity of the suspension medium is analyzed in relation to molecular weight distribution and particle morphology.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1989.070370111
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  • 4
    Electronic Resource
    Electronic Resource
    Quantitative analysis of ethylenediamine in plasma by capillary column gas chromatography (1986)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 9 (1986), S. 548-554 
    Details
    ISSN: 0935-6304
    Keywords: Gas liquid chromatography (GLC) ; Fused silica capillary columns ; Alkali flame ionization detection (AFID) ; Mass spectrometry (MS) ; Quantitation in human serum ; Ethylenediamine ; Aminophylline ; Small molecular weight amines and diamines ; m-Toluoyl derivatives ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A specific and sensitive method for the determination of ethylenediamine in human plasma is described. The aqueous sample is treated with m-toluoyl chloride, yielding the N,N′-bis(m-toluoyl) derivative of the diamine, which is extracted into dichloromethane and quantitated after “on column” methylation by capillary gas liquid chromatography with alkali flame ionization detection. The corresponding derivative of putrescine serves as internal standard. The assay is reproducible and calibration curves are linear over the concentration range 0.05 to 10 μg · ml-1. The lower detection limit is about 10 ng · ml-1. The structures of the compounds of interest eluting from the capillary column are examined by gas liquid chromatography/mass spectrometry. The assay has been applied to the analysis of ethylenediamine in plasma following the administration of aminophylline and ethylenediamine in a cross-over study to patients with bronchopulmonary diseases. The method also proves suitable for measuring other primary and secondary amines and diamines in aqueous solutions by gas liquid chromatography.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jhrc.1240091002
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  • 5
    Electronic Resource
    Electronic Resource
    Wechselwirkungen zwischen Kriechverformung und HeißgaskorrosionVortrag, gehalten auf dem gemeinsam mit der DECHEMA veranstalteten Symposium der VDI-Gesellschaft Werkstofftechnik „Spannungs- und dehnungsinduzierte Korrosionsprozesse“ am 8. und 9. Juni 1978 in Baden-Baden (1978)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 29 (1978), S. 691-703 
    Details
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Interactions between creep deformation and hot gas corrosionThe paper starts with a short explanation of the basic processes during the high temperature corrosion and of deformation under creep stress.Corrosion may give rise to an increase or a decrease of creep resistance, or it may result in an increase of the stress applied. The individual mechanisms are explained and, as far as possible, illustrated by examples. As a rule, however, several factors act simultaneously. The concerted actions is further complicated by back effects of a creep deformation on the corrosion processes. In the case of iron and nickel base alloys there exist obviously critical strain rates beyond which corrosion is enhanced and then proceeds more pronouncedly at the grain boundaries. It is also possible that then internal corrosion processes are triggered, in particular, in the grain boundary regions.While a qualitative assessment of the relationships between corrosion and creep deformation is possible, the feasibility of a quantitative description is still far away. As a rule, however, the aspect of a strength decrease will prevail although, in principle, corrosion may give rise to a strengthening, too.
    Notes: Einleitend werden kurz die Grundvorgänge der Heißgaskorrosion und der Verformung unter Zeitstandbeanspruchung erläutert.Die Korrosion kann den Kriechwiderstand erhöhen oder erniedrigen oder aber auch die anliegende Spannung vergrößern. Die einzelnen Mechanismen werden erläutert und - soweit möglich - durch Beispiele belegt. In der Regel wirken jedoch gleichzeitig mehrere Faktoren ein. Das Zusammenspiel wird durch Rückwirkungen der Kriechverformung auf die Korrosionsvorgänge weiter kompliziert. Für Eisen- und Nickelbasislegierungen gibt es offenbar kritische Dehngeschwindigkeiten, bei deren Überschreiten die Korrosion verstärkt und stärker korngrenzenorientiert abläuft. Auch innere Korrosionsvorgänge können dadurch besonders im Korngrenzenbereich ausgelöst werden.Während die Zusammenhänge zwischen Korrosion und Kriechverformung qualitativ überschaubar sind, liegt die Möglichkeit einer quantitativen Beschreibung noch in weiter Ferne. In der Regel werden die „Negativ-Punkte“ überwiegen, obgleich im Prinzip die Korrosion auch eine Verfestigung bewirken kann.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19780291103
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  • 6
    Electronic Resource
    Electronic Resource
    Continuous reactive processing I: Reactive coating (1985)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 541-547 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 big success of the reaction injection molding (RIM) process has brought about a marked interest in reacting polymer processing. In the present work, we study the technical feasibility of a continuous process to coat metallic conductors using reacting polymers. In the envisioned system, RIM type reactants are mixed and then injected into a tubular reactor through the center of which we pass the cable to be coated. The predictions of the mathematical model developed show that a feasible process can be designed by adequate control of the heat transfer phenomena. The process needs in general, a low reactor temperature and a high cable temperature.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760250906
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  • 7
    Electronic Resource
    Electronic Resource
    Photochemie und Photophysik von 3-(2-Isoxazolinyl)-phenylketonenHerrn Prof. Dr. E. Schmitz zum 60. Geburtstag gewidmet (1988)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 330 (1988), S. 735-747 
    Details
    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
    URL: http://dx.doi.org/10.1002/prac.19883300508
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  • 8
    Electronic Resource
    Electronic Resource
    Reaktionen von elementarem Schwefel mit halogenierten MethanenProfessor Rudolf Hoppe zum 65. Geburtstage am 29. Oktober 1987 gewidmet (1987)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 553 (1987), S. 239-247 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19875531029
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  • 9
    Electronic Resource
    Electronic Resource
    Zur Kenntnis von nur im festen Zustand existenzfähigen 1:1-Verbindungen zwischen Antimon(III)-Halogeniden und 1,3,5-Trithiacyclohexan (s-Trithian) (1977)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 437 (1977), S. 149-154 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Characterization of Weak Bonded Solid 1:1 Adducts Formed between Antimony(III) Halogenides and s-TrithianeCrystalline 1:1 addition compounds are formed on cooling hot solutions of antimony(III) halides and s-trithiane in benzene or toluene. Their preparation, physical properties and vibrational spectra are described.
    Notes: Aus den Gemischen heißer Lösungen von s-Trithian und Antimon(III)-Halogeniden in Benzol oder Toluol kristallisieren beim Erkalten 1:1-Additionsverbindungen. Ihre Darstellung, physikalischen Eigenschaften und Schwingungsspektren werden beschrieben.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19774370119
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  • 10
    Electronic Resource
    Electronic Resource
    Zum nukleophilen Abbau von Tris(pentasulfido)platinat(IV), [Pt(S5)3]2-, und Bis(pentasulfido)platinat(II),[Pt(S5)2]2- (1979)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 452 (1979), S. 112-122 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Nucleophilic Degradation of Tris(pentasulfido)platinum(IV), [Pt(S5)3]2-, and Bis(pentasulfido)platinum(II), [Pt(S5)2]2-The behaviour of [Pt(S5)3]2-, (I), towards sulfite, arsenite, sulfide, hydroxide, and triphenylphosphine has been studied qualitatively and quantitatively. With stoichiometric amounts of nucleophile one ring is degraded; the reaction product [Pt(S5)2]2-, (II), can be isolated. With excess of nucleophile all sulfur atoms are taken off from the platinum; with triphenylphosphine, however, (PPh3)2PtS4, (III), is formed. A mechanistic interpretation of the course of the reaction is given and supported by kinetic studies.
    Notes: Das Verhalten von [Pt(S5)3]2-, (I), gegenüber Sulfit, Arsenit, Sulfid, Hydroxid und Triphenylphosphin wird qualitativ und quantitativ untersucht. Mit stöchiometrischen Mengen an Nukleophil wird ein Ring abgebaut; als Reaktionsprodukt kann [Pt(S5)2]2-, (II), isoliert werden. Mit Überschuß an Nukleophil werden alle Schwefelatome vom Platin abgelöst; mit Triphenylphosphin entsteht dagegen (PPh3)2PtS4, (III). Der Reaktionsablauf wird mechanistisch gedeutet und durch kinetische Untersuchungen erhärtet.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19794520116
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