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  • 1
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molecular Geometry and Excited Electronic States. XXIV. Theoretical Contribution to the S0 and S1 Molecular Structure and to the Sp ← S0 Electronic Spectral Behaviour of 1,4-Distyryl Benzene an of its Doubly-Charged IonsFor selected configurations of 1,4-distyryl benzene and its doubly-charged ions the completely-optimized molecular geometries of the S0 and S1 states are presented. The structural peculiarities and differences are discussed. The Sp ← S0 electronic spectral data calculated on this basis are given and compared with available experimental results.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 28 (1945), S. 576-582 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 28 (1945), S. 1677-1684 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic 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
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 30 (1965), S. 256-261 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei der thermischen oder photolytischen Zersetzung von Di-tert.-butylperoxid in Methanol, Äthanol, n-Propanol, Isopropanol und Benzylalkohol werden Äthylenglykol, 2,3-Butylenglykol, 3,4-Hexylenglykol, Pinakol und Hydrobenzoin mit Ausbeuten von 15 bis 70% gebildet. Bei der thermischen Zersetzung von Di-tert.-butylperoxid in einem Methanol-Äthanol-Gemisch bzw. Methanol-Äthylenglykol-Gemisch entstehen 1,2-Propylenglykol neben Äthylenglykol und 2,3-Butylenglykol bzw. Glycerin neben Äthylenglykol und Erythrit.
    Additional Material: 1 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 613 (1958), S. 137-144 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Zur Bestimmung der Reduzierbarkeit von Tetrazoliumsalzen werden diese mit halbreduzierten Redoxfarbstoffen in modifizierten THUNBERG-Gefäßen zusammengebracht. Das Eintreten oder Ausbleiben der Färbung zeigt an, zwischen welchen Redox-Potentialwerten das Tetrazoliumsalz einzuordnen ist. Auf Grund der Eigenschaft der Tetrazoliumsalze, in ihrer Reduzierbarkeit weitgehend pH-unabhängig zu sein, während das Potential des Bezugssystems pH-abhängig ist, bieten sich mit einem Redox-Farbstoff zahlreiche zur nahen Potentialeingrenzung geeignete Bezugs-Redoxpotentiale. Je nach Tetrazoliumsalz wurden Potentiale der Reduzierbarkeit zwischen  -  290 und + 110mV gemessen.
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 393 (1912), S. 29-60 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 7
    ISSN: 0170-2041
    Keywords: Resolution, kinetic ; Chiral tertiary amines ; Chiral esters ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kinetic Resolutions Starting with rac-Alcohols or rac-Acyl Halides Using Optically Active Inductor BasesIn the reaction of one mole equivalent of achiral acyl halides with two equivalents of rac-alcohols in the presence of one equivalent of an optically active inductor base (tertiary amine) partially optically active esters and partially optically active alcohols are formed, having in some cases high optical purity (60 - 70%). The alcohol moiety of the ester and the unchanged alcohol are of opposite configuration. Treatment of two equivalents of rac-acylhalides with one equivalent of an achiral alcohol and an inductor base also leads to a high degree of optical induction. The carbonic acid moiety in the ester and the unchanged acid are of opposite configuration. The optical induction is influenced a) by the ligands linked to the reaction centers, b) by the relative quantities of the reacting partners, c) by the solvent, and d) by the temperature.
    Notes: Bei der Umsetzung eines Moläquivalents achiraler Carbonsäurehalogenide mit zwei Moläquivalenten rac-Alkoholen entstehen unter Mitwirkung von einem Moläquivalent einer optisch aktiven Induktorbase (tertiäres Amin) partiell optisch aktive Ester sowie partiell optisch aktive Alkohole in zum Teil hoher optischer Reinheit (60 - 70%). Der im Ester gebundene Anteil an Alkohol sowie der nicht umgesetzte Alkohol haben entgegengesetzte Konfiguration. Der Induktionsgrad ist ähnlich hoch, wenn man zwei Moläquivalente eines rac-Carbonsäurehalogenids mit je einem Moläquivalent eines achiralen Alkohols und einer Induktorbase umsetzt. Der Carbonsäureanteil im Ester und die freie Säure haben entgegengesetzte Konfiguration. Die optischen Induktionen werden beeinflußt a) durch die Art der mit den Reaktionszentren verknüpften Liganden, b) durch die relativen Mengen der Reaktionspartner, c) durch das Lösungsmittel und d) durch die Temperatur.
    Additional Material: 8 Tab.
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  • 8
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2004. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 109 (2004): C05004, doi:10.1029/2003JC002094.
    Description: Rates of turbulent kinetic energy (TKE) production and buoyancy flux in the region immediately seaward (~1 km) of a highly stratified estuarine front at the mouth of the Fraser River (British Columbia, Canada) are calculated using a control volume approach. The calculations are based on field data obtained from shipboard instrumentation, specifically velocity data from a ship mounted acoustic Doppler current profiler (ADCP), and salinity data from a towed conductivity-temperature-depth (CTD) unit. The results allow for the calculation of vertical velocities in the water column, and the total vertical transport of salt and momentum. The vertical turbulent transport quantities (inline equation, inline equation) can then be estimated as the difference between the total transport and the advective transport. Estimated production is on the order of 10−3 m2 s−3, yielding a value of ɛ(νN2)−1 on the order of 104. This rate of TKE production is at the upper limit of reported values for ocean and coastal environments. Flux Richardson numbers in this highly energetic system generally range from 0.15 to 0.2, with most mixing occurring at gradient Richardson numbers slightly less than inline equation. These values compare favorably with other values in the literature that are associated with turbulence observations from regimes characterized by scales several orders of magnitude smaller than are present in the Fraser River.
    Description: This work was performed as a part of D. MacDonald’s Ph.D. thesis, and was funded by Office of Naval Research grants N000-14-97-10134 and N000-14-97- 10566, National Science Foundation grant OCE-9906787, a National Science Foundation graduate fellowship, and support from the WHOI Academic Programs Office.
    Keywords: Turbulence ; Entrainment ; Estuary
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 9
    Publication Date: 2022-05-25
    Description: © The Author(s), 2014. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Geophysical Research Letters 41 (2014): 8987–8993, doi:10.1002/2014GL062274.
    Description: Observations at the Columbia River plume show that wave breaking is an important source of turbulence at the offshore front, which may contribute to plume mixing. The lateral gradient of current associated with the plume front is sufficient to block (and break) shorter waves. The intense whitecapping that then occurs at the front is a significant source of turbulence, which diffuses downward from the surface according to a scaling determined by the wave height and the gradient of wave energy flux. This process is distinct from the shear-driven mixing that occurs at the interface of river water and ocean water. Observations with and without short waves are examined, especially in two cases in which the background conditions (i.e., tidal flows and river discharge) are otherwise identical.
    Description: This work was supported by the Office of Naval Research, as part of the Data Assimilation and Remote Sensing for Littoral Applications (DARLA) project and in coordination with the Rivers and Inlets (RIVET) program.
    Keywords: Wave breaking ; Turbulence ; Mixing ; Wave-current interaction ; River plume
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 10
    Publication Date: 2022-05-25
    Description: © 2008 The Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License. The definitive version was published in Environmental Fluid Mechanics 8 (2008): 495-509, doi:10.1007/s10652-008-9107-2.
    Description: Estuarine turbulence is notable in that both the dissipation rate and the buoyancy frequency extend to much higher values than in other natural environments. The high dissipation rates lead to a distinct inertial subrange in the velocity and scalar spectra, which can be exploited for quantifying the turbulence quantities. However, high buoyancy frequencies lead to small Ozmidov scales, which require high sampling rates and small spatial aperture to resolve the turbulent fluxes. A set of observations in a highly stratified estuary demonstrate the effectiveness of a vessel-mounted turbulence array for resolving turbulent processes, and for relating the turbulence to the forcing by the Reynolds-averaged flow. The observations focus on the ebb, when most of the buoyancy flux occurs. Three stages of mixing are observed: (1) intermittent and localized but intense shear instability during the early ebb; (2) continuous and relatively homogeneous shear-induced mixing during the mid-ebb, and weakly stratified, boundary-layer mixing during the late ebb. The mixing efficiency as quantified by the flux Richardson number Rf was frequently observed to be higher than the canonical value of 0.15 from Osborn (J Phys Oceanogr 10:83–89, 1980). The high efficiency may be linked to the temporal–spatial evolution of shear instabilities.
    Description: The funding for this research was obtained from ONR Grant N00014-06-1-0292 and NSF Grant OCE-0729547.
    Keywords: Turbulence ; Estuaries ; Shear instability ; Buoyancy flux
    Repository Name: Woods Hole Open Access Server
    Type: Article
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