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  • Articles  (38)
  • Chemistry and Pharmacology  (35)
  • Process Engineering, Biotechnology, Nutrition Technology  (9)
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  • Articles  (38)
Journal
  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 4904-4910 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The first excited singlet state S1 vibrational dynamics of aniline(N2)1 clusters are studied and compared to previous results on aniline(CH4)1 and aniline(Ar)1. Intramolecular vibrational energy redistribution (IVR) and vibrational predissociation (VP) rates fall between the two extremes of the CH4 (fast IVR, slow VP) and Ar (slow IVR, fast VP) cluster results as is predicted by a serial IVR/VP model using Fermi's golden rule to describe IVR processes and a restricted Rice–Ramsperger–Kassel–Marcus (RRKM) theory to describe unimolecular VP rates. The density of states is the most important factor determining the rates. Two product states, 00 and 10b1, of bare aniline and one intermediate state ∼(00) in the overall IVR/VP process are observed and time resolved measurements are obtained for the 000 and ∼(000) transitions. The results are modeled with the serial mechanism described above.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 3290-3301 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Excited state intramolecular and intermolecular proton transfer reactions in cold, isolated 2-allylphenol, 2-propenylphenol and 2-propylphenol, and their clusters with water and ammonia are investigated employing a combination of spectroscopic techniques (mass resolved excitation, threshold photoionization, dispersed emission), a semiempirical calculation (MOPAC 5) and a potential energy calculation of cluster structure. Threshold photoionization spectroscopy proves to be useful for the identification of molecular conformers in these systems but has mixed results for the identification of proton transfer in their clusters. The total collection of generated data suggests the following conclusions: (1) isolated, cold 2-allylphenol displays only one conformation which appears to have a significant stabilizing intramolecular interaction between the allyl group double bond and the hydroxyl group hydrogen atom; (2) 2-propenylphenol displays only one conformer; (3) 2-propylphenol has many conformations—probably more than five under the experimental conditions; (4) no evidence of intramolecular proton transfer can be found for these three isolated cold molecules; (5) no evidence for intermolecular proton transfer in water clusters has been found by any of the above techniques; and (6) evidence is found for intermolecular proton transfer in 2-allyl- and 2-propenylphenol(NH3)n, n≥3, in dispersed emission spectra. Dispersed emission spectra of 2-propylphenol(NH3)n n≥3 are too weak to yield conclusive evidence for intermolecular excited state proton transfer. Potential energy minimization calculations of cluster geometry suggest that the difference between water and ammonia cluster behavior with regard to proton transfer arises because water molecules hydrogen bond with the hydroxyl group (both OH⋅⋅⋅OH2 and HO⋅⋅⋅HOH) and each other while ammonia molecules are more evenly distributed over the entire molecular structure of the phenol moiety. Apparently, for efficient proton transfer to occur in clusters, the proton affinity of the solvent must be large and both the anion and the proton must be well solvated (stabilized) by the solvent.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 41 (1976), S. 0 
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The kinetics of crystallization of cassava starch during aging were studied at different temperatures using the expression θ= exp(-ktn), where θ is the fraction of uncrystallized material remaining after time t. The values for the rate constant (k) indicated that the firming process for the cassava starch gels was characterized by a negative temperature coefficient. The Avrami exponent (n) was found to be unity over the range of temperatures studied (2-30° C), suggesting that the mechanism of starch crystallizatión is instantaneous nucleation followed by rod-like growth of ciystals.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 7421-7435 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 33 (1993), S. 1361-1367 
    ISSN: 0031-9422
    Keywords: 23-O-β-d-glucopyranosylbrassinolide ; Leguminosae ; Vigna radiata ; brassinolide ; brassinosteroid ; castasterone ; glucoside. ; metabolism ; mung bean
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Tetrahedron Letters 35 (1994), S. 1731-1734 
    ISSN: 0040-4039
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Tetrahedron Letters 33 (1992), S. 2561-2564 
    ISSN: 0040-4039
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 378 (1995), S. 260-263 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] There are two possible mechanisms of double proton transfer in these model base pairs: a stepwise transfer from the base-pair structure (B-PS) to the tautomer structure (TS) through an intermediate (zwitterionic) structure (IS), or a direct cooperative transfer of B-PS to TS (Fig. \a). Since the ...
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Applied microbiology and biotechnology 49 (1998), S. 573-578 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract On the basis of mutational analysis, the genes for phosphonate uptake and degradation in Escherichia coli were shown to be organized in a 10.9-kb operon of 14 genes (named phnC to phnP) and induced by phosphate (Pi) starvation [Metcalf and Wanner (1993) J Bacteriol 175: 3430–3442]. The repression of phosphonate utilization by Pi has hindered both the biochemical characterization of the carbon-phosphorus (C-P) lyase activity and the development of improved methods for phosphonate biodegradation in biotechnology. We have cloned the genes phnG to phnP (associated with C-P lyase activity) with the lac promoter to provide expression of C-P lyase in the presence of Pi. A number of strains lacking portions of the phn operon have been constructed. In vivo complementation of the strains, in which phnC to phnP (including both Pn transport and catalysis genes) or phnH to phnP (including only catalysis genes) was deleted, with plasmids carrying various fragments of the phn operon revealed that the expression of phnC-phnP gene products is essential to restore growth on minimal medium with phosphonate as the sole phosphorus source, while phnG-phnM gene products are required for C-P lyase activity as assessed by in vivo methane production from methylphosphonic acid. The minimum size of the DNA required for the whole-cell C-P lyase activity has been determined to be a 5.8-kb fragment, encompassing the phnG to phnM genes. Therefore, there is no requirement for the phnCDE-encoded phosphonate transport system, suggesting that cleavage of the C-P bond may occur on the outer surface of the inner membrane of E. coli cells, releasing the carbon moiety into the periplasm. These data are in agreement with the observation that phosphonates cannot serve as the carbon source for E.␣coli growth.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 27 (1997), S. 1118-1121 
    ISSN: 1572-8838
    Keywords: Ultraviolet curing ; Acrylates ; Lithium polymer electrolytes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Type of Medium: Electronic Resource
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