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  • Chemistry  (403)
  • 1980-1984  (250)
  • 1970-1974  (139)
  • 1945-1949  (14)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 22 (1983), S. 48-48 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1984), S. 149-150 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 3
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass spectra of the three isomeric vinylimidazoles have been compared and the structures of the fragment ions [C3H4N2]+· and [C5H5N2]+ have been investigated by collisionally activated dissociation mass spectrometry. The greater part of the non-decomposing ions m/z 68 from 2-vinylimidazole and from 2-imidazolecarboxylic acid methyl ester, and a minor part of this ion formed from the free acid, all have the same structure: the imidazole ring system, with hydrogens at both nitrogen atoms but none at C(2). An analogous structure, with an ethyl group at C(2), is proposed for the m/z 93 ion from 2-vinylimidazole.
    Additional Material: 2 Ill.
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  • 4
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 195Pt-, 31P- and 15N-NMR. data are presented for [PtCl2 (t-Bu 15N=CH—CH=15N (t-Bu)) (η2-styrene)] (1), trans-[{PtCl2 (PBu3)}2 (t-Bu 15N=CH—CH=15N (t-Bu))] (2), trans-[PtCl2 (t-Bu 15N=CH—CH=15N (t-Bu)) (PBu3)] (3) and various complexes of the type trans-[PtCl2 (N-ligand) (PBu3)]. In solution the gross structural features of 1 and 2 are shown to be in agreement with those found in the solid state; namely, 1 contains five-coordinate Pt and 2 is dinuclear. In 3 Pt is four-coordinate with only one N-atom of the diimine ligand being coordinated at -50° in CD2Cl2. The NMR. data for 2 and 3 are compared with those of trans-[PtCl2 (N-ligand) (PBu3)] (N-ligand = pyridine, 2, 6-dimethylpyridine, (15N)-hexylamine, (15N)-t-butylamine and (15N)-aniline) and are discussed in terms of the donor and acceptor properties of the N-ligands.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 22 (1980), S. 643-649 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 7 (1984), S. 607-614 
    ISSN: 0935-6304
    Keywords: Gas chromatography, GC ; Fused silica capillary columns ; CP-MAS NMR ; Silylation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of temperature, water content, and the type of reagent on the silylation of fused silica capillaries was studied by 29Si and 13C CP-MAS NMR. Fumed silica (Cab-O-Sil M5), which is essentially a highly dispersed vitreous quartz with a surface comparable to that of fused silica capillary columns, was selected as a model material.Hexamethyldisilazane (HMDS) and 1,2-diphenyl-1,1,3,3-tetraphenyldisilazane (DPTMDS), which were used as silylation reagents, yielded trimethyl- and dimethylphenylsilyl surface groups respectively at lower temperatures (〈 350°C and 〈250°C respectively). At higher temperatures, increasingly more dimethylsilyl groups are formed, with the silicon bound to two oxygen atoms. This process occurs for DPTMDS at a considerably lower temperature than for HMDS. The formation of silyl groups on the surface and the disappearance of hydroxyl groups are followed independently. The 13C NMR and GC-MS of the reaction products showed that with DPTMDS, the formation of two Si-O-Si links is accompanied by a loss of phenyl groups rather than of methyl groups.After the Cab-O-Sil had been dried over P2O5, the formation of these double links occurred for HMDS only at temperatures above 460°C and for DPTMDS at 400°C. Thus we concluded that water supplies oxygen atoms for double Si-O-Si links (possibly crosslinks) necessary for efficient deactivation. This may explain the less successful silanization of fused silica capillaries because their water content is lower than that of glass capillaries.
    Additional Material: 9 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 7 (1980), S. 473-483 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: During the last decade, a considerable amount of information has been gathered on the organic composition of aerosols, mostly sampled by Hi-Vol filtration, and analysed by gas chromatography or gas chromatography mass spectrometry. From our research, it appears that care should be taken in the use of such data for the evaluation of health hazards, resulting from air pollution. The following facts must be considered.(1) The conventional Hi- Vol filtration sampling technique can be subject to several sampling artifacts, such as volatilization from and chemical reaction on the filter. Indeed, a series of compounds of intermediate volatility has been shown to evaporate from particles on the filter, when exposed to large air volumes. Low molecular weight compounds are predominant in the gas phase, and high molecular weight ones in the particulate phase. Furthermore, some pollutants on collected particles can react with molecular or radical species, present in the atmosphere: e.g. the carcinogen benzo (a)pyrene can be degraded very rapidly by traces of ozone to highly polar compounds. (2) Besides pollutants of anthropogenic origin, natural sources may also contribute to the aerosol burden. Thus, the presence of the higher odd carbon numbered n-alkanes reflects the contribution from vegetation (plant waxes). The possible synergistic activity of these compounds in combination with carcinogens, justifies the monitoring of these contaminants in aerosols. (3) Since the retention of particles in the respiratory tract strongly depends on particle size, measurements of total pollutant concentrations have to be supplemented with particle size distribution data. The analysis of several size fractionated samples, taken at suburban as well as at remote rural and sea shore sites, allows the evaluation of the dilution of particulate organics and of the differences in particle size distributions in the background areas. Most pollutants are almost exclusively distributed over the respirable particle size range (below 3 μm) and any observed distribution shifts remain within this range. In conclusion, a realistic estimate is presented of the fractions deposited in and extracted by the tissues of the respiratory tract. These are directly responsible for the health hazards, associated with breathing aerosol particles. It follows that a nearly constant fraction of a given pollutant, enters the bloodstream, irrespective of the sampling site, and thus health hazards remain closely related to the total concentration levels.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 12 (1972), S. 358-363 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: The birefringences of injection molded plates and the birefringence during steady, isothermal shear flow were compared for some amorphous polymers. The materials studied were a polystyrene, a “toughened” polystyrene and an acrylonitrile-butadiene-styrene copolymer. The birefringence of the plates, notably the maximum value for the average over the thickness was found to be related to the shear stress at the cavity wall that had occurred during the mold filling process. This relationship was independent of temperature. To a good approximation, it was also the same as the relationship between the flow birefringence and the shear stress at the wall in isothermal channel flow. It thus appears that the anisotropy of injection molded objects is dominated by the shear stresses during the mold filling process regardless of the temperature and of the macroscopic rate of deformation.
    Additional Material: 12 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 4265-4277 
    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: Melt polymerization conditions for D,L-lactide initiated with tetraphenyltin were studied with regard to polymer molecular weight and weight distributions. “Single” polymerization, “multiple” polymerization (four or eight reactions at the same time), and time-dependent studies are described. Single polymerizations using constant initiator concentrations resulted in a broad scattering of nonreproducible molecular weight values. Multiple polymerizations at constant initiator concentrations, however, resulted in nearly identical molecular weight profiles. Multiple polymerizations at different initiator concentrations did not show an inverse dependency of initiator concentration on polymer molecular weight. Both the single and multiple melt polymerizations resulted in rather broad molecular weight distributions. The presence of hydrolysis products of lactide during the melt polymerization most likely has a detrimental effect on molecular weight. After a short induction period the rather slow polymerization of D,L-lactide resulted in a maximal molecular weight followed by a slight decrease in molecular weight to a constant value. It is concluded that the polymerization of D,L-lactide in the melt initiated with tetraphenyltin does not proceed through a “living” mechanism.
    Additional Material: 3 Ill.
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  • 10
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
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