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  • Chemistry  (13)
  • ARA  (1)
  • F10
  • 1990-1994  (14)
  • 1992  (14)
  • 1
    Electronic Resource
    Electronic Resource
    Effect of the insecticide methidathion on agricultural soil microflora (1992)
    Springer
    Biology and fertility of soils 13 (1992), S. 173-175 
    Details
    ISSN: 1432-0789
    Keywords: Methidathion ; Soil microflora ; Enumeration of functional bacterial groups ; Acetylene reduction assay ; ARA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary We studied the effects of the organophosphorus insecticide methidathion, at concentrations of 10, 50, 100, 200 and 300 μg g-1 in an agricultural soil, on fungi, total bacterial populations, aerobic N2-fixing bacteria, denitrifying bacteria, nitrifying bacteria (phases I and II), and nitrogenase activity (acetylene reduction assay). The presence of 10–300 μg g-1 of methidathion significantly increased fungal populations (colony-forming units). Denitrifying bacteria, aerobic N2-fixing bacteria and N2 fixation were significantly increased at concentrations of 50–300 μg g-1. The total number of bacteria increased significantly at concentrations of 100–300 μg g-1. Nitrifying bacteria decreased initially at concentrations of 300 μg g-1, but recovered rapidly to levels similar to those in the control soil without the insecticide.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00336275
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  • 2
    Electronic Resource
    Electronic Resource
    Polymerization of furfuryl alcohol with trifluoroacetic acid: the influence of experimental conditions (1992)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 193 (1992), S. 1-9 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Furfuryl alcohol was polymerized by trifluoroacetic acid in methylene chloride to give a colored polymer. This polymer possesses two main sequences in which the furan rings are connected by methylene groups (sequence 1) or by dimethylene ether groups (sequence 2). The polymer is not linear but highly branched, as detected by 1H and 13C NMR spectroscopy. Variations of the experimental conditions, such as the presence of air, the trifluoroacetic acid concentration, the reaction temperature and the solvent, do not allow a significant increase in the linear structure of the polymer. However, an increase in the acid concentration or an increase in temperature produce a decrease in the ether-bridged structure (sequences 2).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1992.021930101
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  • 3
    Electronic Resource
    Electronic Resource
    Stereoselective nucleophilic substitution of poly(vinyl chloride) with sodium thiophenate in cyclohexanone solution: Influence of the reaction temperature on the mechanism (1992)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 99-104 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nucleophilic substitution of PVC with sodium thiophenate was carried out in cyclohexanone solution at 5, 25, 40, 60, and 70°C. The initial rate obeys an Arrhenius law from 25 to 60°C, with an activation energy of 70 kJ/mol. Conversion limits are observed which strongly depend on the temperature. The stereoselectivity of the reaction with respect to the configurational triads does not depend on the temperature: the distribution of configurations is only dependent on the conversion. Assuming an SN2 substitution mechanism governed by steric factors, the Monte Carlo simulation procedure described in a prior study is shown to give a good account for all temperatures above 40°C assuming for the mm, mr or rm, and rr triads a reactivity such as Rmm = 2 Rmr and Rrr nil at low temperature and very low at temperatures ≥ 40°C. The low conversion limits observed at 5 and 25°C cannot be explained by a limited accessibility of a part of the polymer. Finally, it is shown that the elimination reaction, which remains limited, does not interfere with the substitution process.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1992.080300112
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  • 4
    Electronic Resource
    Electronic Resource
    Theoretical approach to cationic polymerization of alkenylfurans. II. Ab initio and semiempirical study of relevant steps in the reaction mechanism (1992)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2497-2502 
    Details
    ISSN: 0887-624X
    Keywords: ab initio ; AM1 ; cationic polymerization ; reaction mechanism ; furans ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: SCF ab initio and AM1 semiempirical calculations with full geometry optimization have been carried out to model the initial steps of alkenylfuran cationic polymerization. Semiempirical procedures have been used to model propagation steps. Proton affinities of the relevant neutral species as well as the heats of formation of probable dimers were calculated. The results allow the explanation of the experimental behavior. The capabilities of the employed methods to describe these type of processes is discussed. It is confirmed that competition between vinyl and ring site attacks is the most important feature in these systems. © 1992 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1992.080301203
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  • 5
    Electronic Resource
    Electronic Resource
    Stabilization of substilisin E in organic solvents by site-directed mutagenesis (1992)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 39 (1992), S. 141-147 
    Details
    ISSN: 0006-3592
    Keywords: protein engineering ; enzymes in organic solvents ; protein stabilization ; subtilisin E ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Subtilisin E was rationally engineered to improve its stability in polar organic solvents such as dimethylformamide (DMF). A charged surface residue, Asp248, was substituted by three amino acids of increasing hydrophobicity, Asn, Ala, and Leu; all three variants were stabilized with respect to wild type in 80% DMF. This stabilization was only observed in the presence of high concentrations of the organic solvent: no stability enhancements were observed in 40% DMF. In contrast, the mutation Asn218 → Ser alters internal hydrogen bonding interactions and stabilizes subtilisin E in both 40% and 80% DMF. This study provides additional evidence that substitution of surface-charged residues is a generally useful mechanism for stabilizing enzymes in organic media and that the stabilizing effects of such substitutions are unique to highly altered solvent environments. The effects of the single amino acid substitutions on free energies of stabilization are additive in the Asp248 → Asn + Asn218 → Ser combination variant, yielding an enzyme that is 3.4 times more stable than wild type in 80% DMF.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260390204
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  • 6
    Electronic Resource
    Electronic Resource
    Enhanced release of rosmarinic acid from Coleus blumei permeabilized by dimethyl sulfoxide (DMSO) while preserving cell viability and growth (1992)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 40 (1992), S. 459-464 
    Details
    ISSN: 0006-3592
    Keywords: permeabilization ; dimethyl sulfoxide ; Coleus blumei ; preconditioning ; cell viability ; rosmarinic acid ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Continuous permeabilization of preconditioned Coleus blumei cells with dimethyl sulfoxide (DMSO) is shown to be an effective strategy for the enhanced release of rosmarinic acid (RA) while preserving cell viability. When nonpreconditioned cells were permeabilized with DMSO, they lost their viability at DMSO concentrations higher than a critical value located between 0.1% and 0.5% DMSO. Product release was low [0.49 g RA/100 g dry cell weight (DCW)] at 0.1% DMSO. Preconditioning cells at 0.1% DMSO ensured high viability at DMSO concentrations of 0.5%, 1.0%, and 1.5%. Product release reached a maximum of 2.85 g RA/100 g DCW at 0.5% DMSO, which was 66.4% of the total rosmarinic acid produced. © 1992 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260400403
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  • 7
    Electronic Resource
    Electronic Resource
    Electron impact mass spectrometry of 3-(2-hydroxyphenylcarbonyl)-4-(o- and p-R-phenyl)-1,2,3,4-tetrahydro-2H-benzo [f]quinolin-2-onesContribution No. 1083 from Institute de Quimica, UNAM, Mexico. (1992)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 27 (1992), S. 121-122 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The major features of the mass spectra of eight substituted quinolones of potential pharmacological interest are reported.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210270210
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  • 8
    Electronic Resource
    Electronic Resource
    Studies on enzymatic resistance and molecular structure by 13C-NMR of cellulosic ethers (1992)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 44 (1992), S. 347-352 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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 viscometric method to evaluate the enzymatic resistance of cellulosic ethers is proposed. The method was applied to samples of hydroxyethylcellulose (HEC) with molar substitution between 1.8 and 2.5. The results are discussed in terms of the values of Degree of Substitution and the average unsubstituted primary hydroxyl groups, obtained by high-resolution 13C-NMR of the neat polymers.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1992.070440218
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  • 9
    Electronic Resource
    Electronic Resource
    Phase behavior and mechanical properties of injection molded poly(ethylene terephthalate)/polyarylate blends (1992)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 1135-1143 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: Directly injection molded blends, composed of poly(ethylene terephthalate) and a polyarylate of bisphenol A, and isophthalic/terephthalic acids have been studied. Both their phase behavior and their mechanical properties after this blending method have been determined. After injection molding, the poly(ethylene terephthalate)/polyarylate blends show a single glass transition by differential scanning calorimetry, although the transition peaks of the blends widen when observed by dynamic mechanical analysis. The calorimetric results show a hindered crystallization of poly(ethylene terephthalate), due to the presence of polyarylate and the occurrence of interchange reactions. The mechanical behavior observed shows an improvement in the small-strain properties of the blends with respect to those of the pure components. The break and impact properties of the blends show negative deviations with respect to linearity. These deviations are less important when high polyarylate content exists in the blends.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1992.070450702
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  • 10
    Electronic Resource
    Electronic Resource
    Polymerization of furfuryl alcohol with trifluoroacetic acid, 2Part 1: cf. ref.10. The formation of difurfuryl ether (1992)
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 13 (1992), S. 517-523 
    Details
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/marc.1992.030131107
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