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  • Organic Chemistry  (9,511)
  • Chemical Engineering  (6,025)
  • Engineering  (4,828)
  • 1995-1999  (7,286)
  • 1980-1984  (7,380)
  • 1970-1974  (5,698)
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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 56 (1973), S. 495-499 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complex formation parameters of macrotetrolide antibiotics with alkali and alkaline earth metal cations are given. The stability constants for the complexes in methanol and ethanol at 30°, as determined by vapour pressure osmometry, and ΔH0, ΔG0, and ΔS0 for some interactions in methanol and ethanol at 25°, measured by microcalorimetry, are compared and discussed.
    Additional Material: 3 Tab.
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 55 (1972), S. 2495-2517 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and the spectral properties of the hitherto unknown 9-methyl-cis-decalin-1,3-dione (16) are described. The keto-enol equilibrium of 16 in various solvents was determined by NMR. spectroscopy. The configuration and conformation of a large number of intermediates and derivatives were determined.
    Additional Material: 7 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 23 (1983), S. 510-515 
    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: A saturated triblock copolymer, poly(styrene-block-ethylene-co-butylene-block-styrene) was chemically crosslinked using trimethylol propane trimethacrylate, TMPTM, and subjected to electron beam radiation. The gel percent, Gehman ten second modulus, and stress relaxation were measured to characterize the materials as a function of crosslinker concentration and radiation level. A time-temperature super-position master curve was generated at 63°C for 3 percent TMPTM and 5 Mrads of radiation, which indicated rubbery plateau behavior at long times of measurement, as opposed to the uncrosslinked material, which continued to creep and flow. The main locus of crosslinking was within the polystyrene phase, which explains reduced creep and stress relaxation only for long times of measurement and/or high temperatures. Based on shifts of the glass transition temperatures, it was estimated that 11 to 16 percent poly(ethylene-co-butylene) was dissolved in the polystyrene phase.
    Additional Material: 7 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    International Journal for Numerical Methods in Fluids 28 (1998), S. 565-568 
    ISSN: 0271-2091
    Keywords: fundamental solution method ; integral equation method ; Navier-Stokes equations ; Engineering ; Numerical Methods and Modeling
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: A complete boundary integral formulation for incompressible Navier-Stokes equations with time discretization by operator splitting is developed using the fundamental solutions of the Helmholtz operator equation with different order. The numerical results for the lift and the drag hysteresis associated with a NACA0012 aerofoil oscillating in pitch show good agreement with available experimental data. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 1 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 10 (1998), S. 362-363 
    ISSN: 0899-0042
    Keywords: Jacobsen's catalyst ; enantiomeric purity determination ; chiral HPLC ; cyclodextrin chiral stationary phases ; enantioseparation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A HPLC method is described for the chiral analysis of the commercially available Jacobsen's catalyst. A hydroxypropyl β-cyclodextrin stationary phase was used in conjunction with a nonaqueous, polar-organic mobile phase. The method can be applied to control the enantiomeric purity of the catalyst, which is of great importance for quality control of that product. High accuracy in the determination of trace levels of the unwanted enantiomer in the presence of large amounts of the desired enantiomer is demonstrated. Chirality 10:362-363, 1998. © 1998 Wiley-Liss, Inc.
    Additional Material: 1 Ill.
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  • 16
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conjugate addition of the chiral, non-racemic alkoxy-enolates 5 and 6 to nitroolefins furnishes the hydroxynitroesters 7-13, which are catalytically hydrogenated to give the lactams 14-18. The configuration of adduct 7 from nitroethylene was elucidated by NMR. analysis of the acetal 20 derived from 7. The assignment establishes that the reaction follows the stereochemical rule of attack depicted in 21 and previously deduced for other electrophiles, i.e. formation of erythro-products of type 3b and 4b. No stereocontrol was found at the newly formed chiral centers in α- and β-position to the NO2 group of 8-12.
    Additional Material: 1 Tab.
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  • 17
    ISSN: 0947-3440
    Keywords: Bond cleavage, C-C kinetics of ; Radicals, stability of ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Products and kinetics of the homolytic thermolyses reactions of the three tertiary amides 6a-c of 2,3,3-triphenylpropanoic acid were studied in solution. The steric effects on the C-C bond homolysis processes were evaluated from MM2 calculations. Taking this into account, we deduced radical stabilization enthalpies RSE for the α-carbamoylbenzyl radicals 3a-c from the activation enthalpies ΔH≠ [RSE (kcal/mol): 8.3 ± 2.8 (3a), 10.3 ± 2.7 (3b), 9.0 ± 2.2 (3c)].
    Additional Material: 5 Tab.
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  • 18
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 16 (1970), S. 112-119 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A modified Redlich-Kwong equation has been applied to the calculation of phase equilibria in multicomponent systems. The two parameters of the Redlich-Kwong equation are treated as temperature functions. They are obtained for each pure component from experimental vapor pressures and liquid densities with the help of a generalized fugacity coefficient correlation for saturated vapors. The need to submit coefficients for pure components is thus eliminated. At least one experimental vapor-liquid equilibrium point is required to establish an interaction constant for each binary system. Applications have been made to binary and multicomponent systems containing hydrocarbons, hydrogen, carbon dioxide, and hydrogen sulfide.
    Additional Material: 6 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 765 (1973), S. 15-19 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Thermal Rearrangement of Arylaldoketene DimersArylaldoketene dimers 5 and 1 with β-lacton- or hydroxy-cyclobutenon structures and their acylated and alkylated derivatives can be thermally rearranged yielding the corresponding derivatives of naphthalene-1,3-diol 3.
    Notes: Aryl-aldoketen-Dimere 5 und 1 mit β-Lacton- bzw. Hydroxy-cyclobutenon-Struktur sowie die acylierten und alkylierten Derivate der letzteren lassen sich thermisch in Abkömmlinge des 1.3-Naphthalin-diols 3 umlagern.
    Additional Material: 1 Tab.
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  • 20
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 760 (1972), S. 171-173 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Chemistry of Dimeric Phenylketene2-Hydroxy-4-oxo-1,3-diphenyl-1-cyclobutene (1), which yields 1,3-diacetoxy-2-phenylnaphthalene in boiling acetic anhydride, can be rearranged in boiling xylene to give 1,3-dihydroxy-2-phenylnaphthalene (2).
    Notes: Es wird gezeigt, daß 2-Hydroxy-4-oxo-1.3-diphenyl-1-cyclobuten (1), welches sich in siedendem Acetanhydrid zum 1.3-Diacetoxy-2-phenyl-naphthalin umlagert, rein thermisch in siedendem Xylol in 1.3-Dihydroxy-2-phenyl-naphthalin (2) übergeführt werden kann.
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