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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 55 (1933), S. 1119-1124 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 2 (1963), S. 61-66 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 21 (1982), S. 35-46 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 82 (1985), S. 3894-3902 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The microwave spectrum of ethyldifluorophosphine, CH3CH2PF2, has been investigated in the region from 18.0 to 39.5 GHz. The spectra of two conformers have been identified. The ground state and seven vibrationally excited states have been assigned for the more stable gauche conformer (phosphorus lone pair with respect to CH3 group), whereas the ground state and one excited state have been assigned for the trans form. Rotational and most quartic centrifugal distortion constants have been determined with A=6784.501(3), B=2930.156(2), C=2352.576(2) MHz for gauche and A=5444.910(3), B=3290.133(3), C=2871.915(3) MHz for trans, both in the ground state. Electric dipole moments were obtained from ground state Stark effect measurements: || μa||=1.990(4), || μb||=0.855(4), || μc||=0.091(7), || μt||=2.168(2) D for gauche and || μa||=1.780(10), || μb||=0, || μc||=1.077(10), || μt||=2.081(10) D for trans. Using a new computer program, a diagnostic least-squares fit of the structural parameters suggests significant structural differences between the conformers, notably the C–C–P angle which changes from 110.7° in the gauche form to 114.9° in the trans form. From a temperature study of the microwave spectrum, it was found that the gauche conformer is at least 80 cm−1 (229 cal/mol) more stable than the trans conformer. These results are compared to similar quantities in some corresponding molecules.
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    International Journal of Industrial Organization 11 (1993), S. 239-260 
    ISSN: 0167-7187
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Economics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Probability theory and related fields 19 (1971), S. 243-256 
    ISSN: 1432-2064
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biospectroscopy 2 (1996), S. 249-258 
    ISSN: 1075-4261
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: The photodegradation of wool keratin is a very complex process that is not well understood. In this work the techniques of Fourier transform Raman and attenuated total reflectance Fourier transform-infrared spectroscopies have been used to study wool samples irradiated in air using a variety of different sources. The spectra obtained from these samples have been compared with those obtained from wool treated with sodium bisulphite, a reagent well known to produce thiol and S-sulfonate groups. As an aid for spectral interpretation the Raman and infrared spectra of cystine and those of the sodium and potassium cysteine-S-sulfonates have also been obtained. The data suggest that there are two different photolytic reaction pathways involving the cystine residues which are dependent on the wavelength of the applied radiation. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 9
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    In:  XXVIII General Assembly of the International Union of Geodesy and Geophysics (IUGG)
    Publication Date: 2023-05-16
    Description: Global mean sea level has been rising and is attributed to anthropogenic climate change forcing. The causes are mainly thermal expansion due to ocean warming and addition of water mass into the ocean from melting of land ice. Regional sea levels can deviate significantly from global mean sea level due to different processes at various spatiotemporal scales. In this study, we examine Australian sea levels and underlying mechanisms based on observations from 1880s to current, including direct sea level measurements by in-situ tide gauges and satellite altimetry, as well as other relevant oceanic and atmospheric observations. We focus on three aspects to explain the regional distribution of Australian sea levels. Firstly, we examine the connection of sea levels with modes of climate variability (e.g., ENSO) and driving physical processes (e.g., wave propagation). Secondly, the regional sea level budget from 1966 to present from selected tide gauges are analysed to identify the dominant factors for sea level trends, including ocean dynamics, sea level fingerprints, vertical land movement and inverse barometer effect. Thirdly, the connection between Australian sea levels and ocean gyre circulation and boundary currents (such as the South Pacific subtropical ocean gyre and East Australian Current) are identified, focusing on coastal sea levels in response to strength and position of ocean gyres and boundary currents. Findings from this historical study improve our understanding of sea level changes and variability around Australia, which will help us to project future sea level changes in coming decades with more confidence and reliability.
    Language: English
    Type: info:eu-repo/semantics/conferenceObject
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  • 10
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    In:  XXVIII General Assembly of the International Union of Geodesy and Geophysics (IUGG)
    Publication Date: 2023-05-25
    Description: Sea-level rise integrates the responses of several components (ocean thermal expansion, mass loss from glaciers and ice sheets, terrestrial water storage). Before the satellite era, global sea-level reconstructions depend on tide-gauge records and ocean observations. However, the available global mean sea level (GMSL) reconstructions using different methods indicate a spread in sealevel trend over 1900-2008 (1.3~2.0 mm/yr). With the improved understanding of the causes of sea-level change, here we update the original Church and White (2011) reconstruction by using the latest observations, taking the time-evolving sea-level fingerprint, sterodynamic sea level (SDSL) climate change pattern and local vertical land motion (VLM) into account. The updated trend of GMSL of 1.6 ± 0.2 mm/yr (90% confidence level) over 1900-2019 is consistent with the sum of contributions of 1.5 ± 0.2 mm/yr, slightly lower than 1.8 ± 0.2 mm/yr from original reconstruction. The lower trend from the updated reconstruction is mainly due to including residual VLM correction. The trends at tide gauge locations from updated reconstruction agree better with the tide gauge observations, with comparable mean trend of 1.7 mm/yr (standard deviation; STD of 2.0 mm/yr) from observation and 1.7 mm/yr (STD of 1.2 mm/yr) from the updated reconstruction. The inclusion of sea-level fingerprint and SDSL climate change pattern are the dominant contributors for improved reconstruction skill on regional scales at tide gauge locations. This update leads to GMSL solution that are consistent with other reconstructions in terms of long-term trend and 30-year running rate.
    Language: English
    Type: info:eu-repo/semantics/conferenceObject
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