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  • 1975-1979  (8)
  • 1970-1974  (5)
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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 74 (1970), S. 1014-1021 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 17 (1978), S. 1691-1693 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 683-685 
    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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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 3754-3756 
    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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  • 5
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Separation of the Intermediates of the Acid Hydrolysis of Tris(salicylaldehydato)chromium(III) and Kinetics of the Acid Hydrolysis of the Cation Tetraaquamono(salicylaldehydato)chromium(III)The intermediates of the acid hydrolysis of tris(salicylaldehydato)chromium(III) were separated and identified by ion exchange and electrophoresis to be the cations diaquabis(salicylaldehydato)chromium(III) and tetraaquamono(salicylaldehydato)chromium(III) (= [Cr(SA)(H2O)4]2+). The hydrolysis of the cation [Cr(SA)(H2O)4]2+ with perchloric acid is of pseudo-first order and leads to the cation [Cr(H2O)6]3+. For constant ionic strength (I = 3) and [HCIO4] = 0.1-3 N kexp = k′ + k″[H+] is deduced. The mechanism is discussed on the basis of the ΔH≠-and ΔS≠ values obtained.
    Notes: Als Zwischenprodukte der Säurehydrolyse von Tris(salicylaldehydato)chrom(III) wurden durch Ionenaustausch und Elektrophorese die Kationen Diaquabis(salicylaldehydato)chrom(III) und Tetraaquamono(salicylaldehydato)chrom(III) (= [Cr(SA)(H2O)4](2+) identifiziert. Die Hydrolyse des [Cr(SA)(H2O)4]2+-Kations mit Perchlorsäure führt in einer Reaktion pseudo-erster Ordnung zum [Cr(H2O)6]3+-Kation. Für konstante Ionenstärke (I = 3) und [HCIO4] = 0.1-3 N gilt: kexp = k′ + k″[H+]. Der Mechanismus wird anhand der ermittelten ΔH≠- und ΔS≠-Werte diskutiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1315-1322 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Influence of Various Anions on the Kinetics of the Acid Hydrolysis of the Cation Tetraaquamono(salicylaldehydato)chromium(III)The kinetics of the acid hydrolysis of the cation tetraaquamono(salicylaldehydato)chromium(III) in perchloric acid were studied at 70°C at constant ionic strength as a function of various anions added to the system. The hydrolysis is strongly accelerated by oxyanions like sulfate and nitrate, while halide anions like chloride and bromide affect the rate only slightly. The findings are explained on the basis of the „cis-effect“ of the oxyanions. The reaction is interpreted by an associative interchange mechanism (Ia).
    Notes: Die Kinetik der Säurehydrolyse des Tetraaquamono(salicylaldehydato)chrom(III)-Kations in perchlorsaurer Lösung wurde in Abhängigkeit vom Zusatz verschiedener Anionen bei 70°C und konstanter Ionenstärke untersucht. Die Hydrolyse wird durch die Oxyanionen Sulfat und Nitrat stark beschleunigt, während die Halogenid-Ionen Chlorid und Bromid die Reaktionsgeschwindigkeit nur geringfügig erhöhen. Dieses Ergebnis wird mit dem „cis-Effekt“ der Oxyanionen erklärt. Der Reaktionsablauf wird mit einem assoziativen Interchange-Mechanismus (Ia) interpretiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 1580-1583 
    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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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 2698-2705 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Exchange Kinetics of [N,N′-Ethylenebis(salicylaldiminato)]copper(II) Complexes in ChloroformThe isotopic copper exchange between mono(pyridine)copper(II) acetate (=CuAc2py) and [N,N′-ethylenebis(5-methoxysalicylaldiminato)]copper(II) ( = CuL) in chloroform as studied in the temperature range 20-50°C can be described by the rate law (9). This rate law is in agreement with a three step exchange mechanism, involving monomeric copper acetate and an „activated“ complex. For the equilibrium between dimeric and monomeric CuAc2py in chloroform Kd = 10-4 mol/litre is obtained by evaluation of the kinetic data.
    Notes: Der isotope Kupferaustausch zwischen Mono(pyridin)kupfer(II)-acetat (=CuAc2py) und [N,N′-Äthylenbis(5-methoxysalicylaldiminato)]kupfer(II) ( = CuL) in Chloroform kann im Bereich 20-50°C durch die Geschwindigkeitsgleichung (9) beschrieben werden. sie ist in Übereinstimmung mit einem aus drei Einzelschritten bestehenden Austauschmechanismus, an dem monomeres Kupferacetat und ein „aktivierter“ Komplex beteiligt sind. Die Auswertung der kinetischen Daten liefert den wert Kd = 10-4 mol/Liter für das Gleichgewicht zwischen dimerem und monomerem CuAc2py in Chloroform.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 842-850 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kinetics of Homogeneous Isotope Exchange Between Cycloalkyl Bromides and Bromide Ions in DimethylsulfoxideThe kinetics of the bimolecular homogeneous isotope exchange between 82Br- labelled cyclopentyl bromide (1), cyclohexyl bromide (2), cycloheptyl bromide (3), cyclooctyl bromide (4) and bromide ions (tetrabutylammonium bromide) was investigated at 50-120° in dimethyl sulfoxide as solvent. The enthalpies of activation are ΔH≠(1) = 13.9, ΔH≠(2) = 26.6, ΔH≠(3) = 17.4, and ΔH≠(4) = 23.2 kcal/mole. The ratio of the rate constants k2 at 25° is \documentclass{article}\pagestyle{empty}\begin{document}$$ k_2 ({\bf 1})\,:\,k_2 ({\bf 2})\,:\,k_2 ({\bf 3})\,:\,k_2 ({\bf 4})\, = 667\,:\,1\,:\,341\,\,19 $$\end{document} The difference in reactivity is compared with the reactivity of the corresponding cycloalkyl chlorides.
    Notes: Die Kinetik des bimolekularen homogenen Isotopenaustausches zwischen 82Br-markiertem Cyclopentylbromid (1), Cyclohexylbromid (2), Cycloheptylbromid (3) bzw. Cyclooctylbromid (4) und Bromid-Ionen (Tetrabutylammoniumbromid) wurde in Dimethylsulfoxid zwischen 50 und 120° untersucht. Die Aktivierungsenthalpien betragen ΔH≠(1)=13.9, ΔH≠(2)=26.6, ΔH≠(3)=17.4 und ΔH≠(4)=23.2 kcal/Mol. Die Geschwindigkeitskonstanten k2stehen bei 25° im Verhältnis \documentclass{article}\pagestyle{empty}\begin{document}$$ k_2 ({\bf 1})\,:\,k_2 ({\bf 2})\,:\,k_2 ({\bf 3})\,:\,k_2 ({\bf 4})\, = 667\,:\,1\,:\,341\,\,19 $$\end{document} Die unterschiedliche Reaktionsfähigkeit wird mit der der entsprechenden Cycloalkylchloride verglichen.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 2691-2697 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kinetics of the Acid Hydrolysis of Tris(salicylaldehydato)chromium(III)The kinetics of the acid hydrolysis of tris(salicylaldehydato)chromium(III) were studied spectro-photometrically in mixtures of 1 N H2SO4, 1 N HClO4, and 6 N HClO4 With ethanol, and in the temperature range 30-50°C. The aquation proceeds via a sequence of three consecutive steps of first order and finally leads to hydrated chromium(III) cation. Two intermediates are observed, the absorption spectra of which were calculated.  -  At 40°C the following ratio of rate constants for the three steps of aquation was obtained (ethanol : 1 N H2SO4 = 1 : 1) k1 : k2 : k3 = 61 : 6.5 : 1. The activation parameters were determined. k3 is strongly dependent on the type of acid applied.
    Notes: Die Kinetik der Säurehydrolyse von Tris(salicylaldehydato)chrom(III) Wurde in Gemischen von 1 N H2SO4, 1 N HClO4 bzw. 6 N HClO4 und Äthanol im Temperaturbereich 30-50° spektro-photometrisch untersucht. Die Aquotisierung verläuft über eine Folge von drei Reaktionen 1. Ordnung und führt schließlich zum hydratisierten Chrom(III)-Kation. Dabei werden zwei Zwischenprodukte beobachtet, deren Absorptionsspektren berechnet wurden.  -  Für die Geschwindig-keitskonstanten der drei Teilschritte gilt bei 40° (Äthanol : 1 N H2SO4 = 1 : 1) k1 : k2 : k3 = 61 : 6.5 : 1. Die Aktivierungsparameter wurden bestimmt. k3 ist stark abhängig von der Art der eingesetzten Säure.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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