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  • 1
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organotin compounds with the general formula R2(X)SnL (where R=Me, Et, n-Bu, Ph; L=the trans-3-(2-furanyl)-2-propenoate anion or the trans-3-(3-methylphenyl)-2-propenoate anion; and X=Cl) have been prepared by redistribution reactions between the R2SnL2 and R2SnX2 compounds. These compounds were characterized by elemental analyses and various spectroscopic techniques such as 1H, 13C, 119Sn NMR, Mass, Mössbauer, and IR spectroscopies. On the basis of these spectroscopic data, it is suggested that these compounds adopt the cis-R2(X)SnO2 geometry. © 1997 John Wiley & Sons, Inc. Heteroatom Chem 8: 273-278, 1997.
    Additional Material: 6 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 7 (1996), S. 233-237 
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanism of the fluxional process occurring in dimeric tetraorganodicarboxylato stannoxanes is presented on the basis of multinuclear NMR studies carried out in noncoordinating solvents. This fluxional process is a consequence of rapid migration of carboxylate groups from one tin atom to the other. It has been proposed that larger carboxylates will also execute this behavior. The effect of cis and trans positions on the fluxional process is discussed. The fluxional process is very fast and could not be stopped even at low temperatures, as measured on the NMR time scale. © 1996 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 96 (1963), S. 1610-1617 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ausgehend von 9-Formyl-fluoren, wurde ein spirocyclisches Cyclohexadienon-Derivat XI synthetisiert. Die Behandlung dieses Ketons mit Acetanhydird und Schwefelsäure führte unter Umlagerung zu Acetoxy-triphenylen. Nach Reduktion der Carbonylgruppe ergab die Umlagerung Triphenylen. Auf ähnliche Weise wurden auch Triphenylencarbonsäure und 2-Phenyl-triphenylen hergestellt.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2353-2355 
    ISSN: 0009-2940
    Keywords: Ylides ; Distonic ions ; Neutralization-reionization mass spectrometry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The recently described (Maier et al.[2]) title compound is not only viable in an argon matrix (10 K) but is also accessible in the gas phase. Electron impact ionization of (CH3)3CCX2NC (X = H, D) gives rise to HCNCX2+, which can be successfully neutralized in a beam experiment.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1171-1173 
    ISSN: 0009-2940
    Keywords: Tandem mass spectrometry ; Collision experiments ; Sulfur-nitrogen clusters ; Electron transfer ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Collision experiments on NS-x (x = 2, 3) clusters are reported. Evidence is presented for the gas-phase existence of the corresponding NS.x and NS+x species. For x = 3, the mass spectra are very much in keeping with a connectivity SS-NS (5) for all three charge states. For x = 2, the experimental data favor the presence of NSS (2); however, the cyclic C2v-symmetric form 3 cannot be ruled out.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 177 (1976), S. 101-120 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Kinetik des Abbaus von Cellulosetriacetat wurde im Chloroform/Acetanhydrid-Gemisch in Gegenwart von Perchlorsäure oder Schwefelsäure als Katalysator untersucht. Die zeitliche Änderung des Molekulargewichts wurde viskosimetrisch verfolgt, unter Verwendung der Maronschen “Einpunkt-Methode” zur Erimittlung der Grenzviskositäten sowie der zugehörigen Mark-Houwink-Konstanten für das Chloroform/Acetanhydrid-Gemisch. Die Abhängigkeit der Geschwindigkeitskonstante 1. Ordnung von der Konzentration des Katalysators, des Acetanhydrids und des Cellulosetriacetats sowie vom Molekulargewicht des Polymers und der Temperatur, wurde untersucht. Die Erklärung der Ergebnisse beruht auf der katalytischen Wirksamkeit von H+ und Ac+ (Acetyliumion) bei der Abbaureaktion, die bereits in ähnlichen Celluloseacetat-Systemen von früheren Autoren beobachtet wurde.
    Notes: The kinetics of the degradation of cellulose triacetate in chloroform/acetic anhydride mixtures containing a perchloric or sulphuric acid catalyst was studied. The change in molecular weight with time was followed viscometrically, employing Maron's singlepoint method to evaluate limiting viscosity number values and using appropriate Mark-Houwink constants for the chloroform/acetic anhydride mixtures. The dependence of the first-order rate constant on concentration of catalyst, acetic anhydride, and cellulose triacetate, as well as polymer molecular weight and temperature was investigated. An explanation of the results, based on both H+ and Ac+ (acetylium ion) acting as the catalytic degradation species, is given; this is also shown to account for the degradation behaviour in similar cellulose acetate systems observed by previous workers.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 322 (1980), S. 816-820 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Zur Reaktion von β-Diketonen mit p-Tosylhydrazin
    Additional Material: 2 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 5 (1991), S. 291-298 
    ISSN: 0886-9383
    Keywords: Absorbance ratio ; Statistical confidence ; Quality control ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ratio measurements are commonly used to address a variety of analytical problems in environmental, forensic and pharmaceutical laboratories. In absorbance ratioing techniques, analytical chemists rely on the spectral features of the analyte(s) of interest. The absorbances at two wavelengths are monitored and the ratio of these two absorbances is computed. This ratio is then used to confirm the identity of the analyte(s) of interest, the purity of a product of the overlap of chromatographic peaks. These decisions often have far-reaching consequences (e.g. the identification of the source, biogenic or petrogenic, of hydrocarbons in biological tissues or water). Given the cost and the liabilities associated with such decisions, it is unfortunate that these ratios are seldom reported with any statistical confidence. The purpose of this study is to delineate the parameters that affect absorbance ratio measurements. The models that can be used to estimate the statistical confidence in these measurements are derived and evaluated experimentally. The results show that these models can estimate the relative standard deviations in absorbance ratios accurately. They can also estimate the effect of signal-to-noise ratio and the choice of wavelengths on the precision of absorbance ratios.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 39 (1993), S. 369-386 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Nonlinear transport processes in disordered systems such as porous media and heterogeneous solids are studied, which are represented by two- or three-dimensional networks of interconnected bonds, by a Bethe network (a branching network with no closed loops) of a given coordination number, or by a continuum in which circular or spherical inclusions have been inserted at random. The bonds represent the pores of the pore space, or the conducting and insulating regions of a disordered solid, to which we assign effective properties (radii or conductances) selected at random from a probability density function. Three types of nonlinear transport processes are considered. (1) The relation between the current q and the potential gradient v is of power-law type (as in, for example, flow of power-law fluids or the electric current in doped polycrystalline semiconductors). (2) The relation between q and v is piecewise linear, characterized by a threshold (as in flow of Bingham fluids or in mechanical or dielectric breakdown of composite solids). (3) A large v is imposed on the system, so that a linear transport theory is not valid. The behavioral study of the effective transport and topological properties of the system, such as the permeability, conductivity, diffusivity, and the shape of the samplespanning cluster of conducting paths shows that in all cases the concepts of percolation theory play a prominent role, even if the system is well connected and percolation may seem not to play any role. For most cases, new effective-medium approximations (EMAs) are derived for estimating effective transport properties. Compared to the case of linear transport, new EMAs are considerably more accurate in predicting the scaling properties of the transport coefficients near a critical point such as the percolation threshold. For a power-law transport process, an exact solution is also derived for the Bethe networks. Using the concepts of percolation theory, scaling laws relating the effective properties to various regimes of transport and to topological properties of the system are also given. A relation between the volumetric flow rate of a power-law fluid in porous media and the macroscopic pressure drop is derived, which contains no adjustable parameter and is valid at any porosity. To test the accuracy of our analytical predictions, Monte Carlo simulations are carried out for several cases. In most cases, good agreement is found between the simulation results and predictions. The extension of the results to other types of nonlinearities is also discussed.
    Additional Material: 11 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 41 (1995), S. 456-468 
    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 thermodynamics and transport properties of Lennard-Jones particles in pillared catalytic clays are studied by molecular dynamics simulation. The clays are represented by parallel sheets separated by a given distance and connected by pillars of a given size. Two different spatial distributions of the pillars are studied to determine their effect on the properties of the system. Calculations did not indicate a strong dependence of the diffusivity on the spatial distribution of the pillars, except at low porosities. The solvation force increases monotonically with decreasing porosity of the clays and increasing density of the molecules. The percolation threshold ϕc of the system is estimated from the diffusivity measurements in the limit of infinitely low sorbate densities. Near ϕc the diffusivity D vanishes according to the power law, D ˜ (ϕ - ϕc)n, where ϕ is the porosity of the system, and n is a universal constant. The simulations yield n ⋍ 1.7. Since 2- percolation systems require n ⋍ 1.3 and 3-D systems n ⋍ 2.0, pillared clays behave as a system with an effective dimensionality between 2 and 3.
    Additional Material: 24 Ill.
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