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  • 1
    Digitale Medien
    Digitale Medien
    Eigenschaften von Chalkogen - Chalkogen-Bindungen, XVII. - Di- und Trisulfane mit sterisch anspruchsvollen Alkyl-Substituenten: Das erste trans-Dialkyldisulfan (1993)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1811-1811 
    Details
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/cber.19931260809
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  • 2
    Digitale Medien
    Digitale Medien
    Isothermal volume relaxation in aged polycarbonate measured by positron annihilation lifetime spectroscopy (1990)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 762-768 
    Details
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The positron annihilation lifetime spectroscopy (PALS) technique is used to measure volume relaxation in physically aged glassy polycarbonate. The relaxation times and activation energy calculated for the isothermal relaxations in the aged polycarbonate are greater than those parameters calculated for unaged polycarbonate. The activation energy of 8.2 kcal/mol in the aged polycarbonate is used to identify the phenyl group motion or the cooperative carbonate-phenyl interaction as the molecular features responsible for the thermally induced open volume relaxations. It is postulated that the open volume relaxation kinetics as measured by PALS can be used as a nondestructive indication of property differences between aged and unaged polycarbonate.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/pen.760301303
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  • 3
    Digitale Medien
    Digitale Medien
    Thermal degradation of polymers. Part III. Vacuum pyrolysis of poly(m-aminostyrene); the products volatile at pyrolysis temperature which are liquid or gaseous at room temperaturePaper presented at Thermal Analysis Group of Society of Analytical Chemistry Burlington House, London, on November 13th, 1968. (1969)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 2033-2043 
    Details
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The products obtained on degradation of poly(m-aminostyrene) in vacuo are described. The effect of molecular weight and pyrolysis temperature are discussed and the behavior of poly(m-aminostyrene) compared with that of polystyrene. Quantitative analytical methods using ultra-violet spectroscopy and gas liquid chromatography are described for m-aminostyrene and m-toluidine. The possible mechanisms of degradation to yield the products are discussed.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/app.1969.070131001
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  • 4
    Digitale Medien
    Digitale Medien
    A positron annihilation lifetime study of isothermal structural relaxation in bisphenol-A polycarbonate (1988)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1541-1552 
    Details
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Positron annihilation lifetime spectroscopy has been used to study the isothermal relaxation response of compression molded bisphenol-A polycarbonate at temperatures of 263, 273, and 303 K. The temperature dependence of both the lifetime and intensity of the ortho-Positronium (o-Ps) pickoff component is discussed in terms of ductile-to-brittle transition behavior and free volume theory. An additive exponential model and the Williams-Watt model were used to analyze the relaxation as a function of temperature and provided results consistent with the anticipated molecular mobility of polycarbonate at sub-Tg temperatures.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/pola.1988.080260605
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  • 5
    Digitale Medien
    Digitale Medien
    Decomposition of organic wastes by Sphaerotilus (1963)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 5 (1963), S. 287-307 
    Details
    ISSN: 0006-3592
    Schlagwort(e): Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: Sphaerotilus is usually present in biological waste treatment processes and is considered to be a nuisance organism because it may cause bulking of activated sludge. However, it may play an important role in the decomposition of putrescible organic matter in properly operated biological waste treatment processes. The research described herein is a study of the variety of types of organic compounds which may be decomposed by Sphaerotilus and the effect of some environmental factors upon the rate of decomposition. Although there are some types of compounds which cannot be decomposed by Sphaerotilus, it is shown that this organism is able to assimilate and oxidize a large variety of organic compounds and that it is tolerant of an extremely wide range of environmental conditions. The role of Sphaerotilus in biological waste treatment is discussed in the light of the data presented.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/bit.260050405
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  • 6
    Digitale Medien
    Digitale Medien
    New insights into the Stereochemistry of 3-AminothioacrylamidesDedicated to Professor Dr. Wolfgang Walter on the Occasion of his 75th Birthday. (1995)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 337 (1995), S. 46-49 
    Details
    ISSN: 0941-1216
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The hitherto unknown stereochemistry of N,N,N′,N′-tetrasubstituted 2-arylthioacrylamides 1 has been determined by X-ray crystal analysis and systematic NMR-investigations. Provided that the 2-aryl group lacks ortho substituents, compounds 1 exist predominantly as Z-isomers. In contrast, the major isomer has an E-s-trans configuration if the 2-aryl group is ortho-substituted. Substitution of the 3-amino group of 1 by glycinates, giving 3-aminothioacrylamides 2, generally preserves the original stereochemistry.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/prac.19953370110
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  • 7
    Digitale Medien
    Digitale Medien
    Structure of the deoxytetranucleotide d-pApTpApT and a sequence-dependent model for poly(dA-dT)Supplementary material on observed and calculated structure factors for d-pApTpApT is available from the authors. (1982)
    New York : Wiley-Blackwell
    Biopolymers 21 (1982), S. 513-533 
    Details
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The x-ray structure of the hydrated ammonium salt of the deoxytetranucleotide d-pApTpApT was determined by Patterson and direct methods at a resolution of 1 Å. The crystal structure contains right-handed double-helical segments formed by complementary Watson-Crick-type hydrogen bonding between the adenine and thymine bases of neighboring molecules. The minihelix contains two base pairs. The chains are antiparallel. The A-T and T-A sequences have different phosphodiester conformations. The deoxyribose-pucker and the sugar-base orientation alternate along the chain depending on the nature of the base (3′-endo for purine and 2′-endo for pyrimidine). The extended structure is stabilized by base-base, base-sugar, and hydrogen-bond interactions. The minihelix of two base pairs provides starting coordinates for model-building studies of the dA-dT polymer. A B-DNA-type polymer structure is described, which has sequence-dependent alternations of both the deoxyribose pucker and the phosphate diester bridge conformation. Such sequence-dependent DNA structures, if present locally in regions such as operator sequences, could facilitate sequence-specific interactions. The crystal study also suggests possible geometrical parameters for the replication fork.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/bip.360210304
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  • 8
    Digitale Medien
    Digitale Medien
    1,5-dimethyl-2,3,3,4-tetrachloro-1,5,2,4-diazadiphosphorinan-6-one and some derivatives. Part II (1997)
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 8 (1997), S. 165-175 
    Details
    ISSN: 1042-7163
    Schlagwort(e): Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The title compound 1 was allowed to react with catechol, 2,3-dihydroxynaphthalene, tetrabromocatechol, resorcinol, saligenin, and 3,5-di-tert-butylcatechol in the presence of triethylamine to form compounds 4a-4d and 4f. Whereas the catechol derivative 4a, the naphthol derivative 4b, and the tetrabromocatechol derivative 4c could be readily obtained, the saligenin derivative 4d and the 3,5-di-tert-butylcatechol derivative 4f were found to be stable only in solution. Contrary to expectation, compound 4e was not formed in the reaction of 1 with resorcinol. The reaction of 1 with 1,2,4,5-tetrahydroxybenzene led to the pentacyclic derivative 4g. Reaction of hydroquinone with 1 led to the formation of the dimeric structure 4h. Crystal structure analyses of 4a and 4b show that the nine-membered rings adopt essentially identical “tub” conformations in which the P and O atoms are coplanar. The P-C-P angles (across the CCl2 bridge) are wide (ca. 119°). © 1997 John Wiley & Sons, Inc.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Thermal degradation of polymers. part IV. Vacuum pyrolysis of poly(m-aminostyrene). The residue and the fraction volatile at pyrolysis temperature involatile at room temperature (1969)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 1555-1567 
    Details
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The effect of the extent of degradation of poly(m-aminostyrene) on the quantity and composition of the residue and the effect of pyrolysis temperature on the fraction volatile at pyrolysis temperature are discussed. The behavior of poly(m-aminostyrene) is compared to that of polystyrene; a significant difference has been found for the behavior of the residue from poly(m-aminostyrene), which is ascribed to a crosslinking reaction involving the amino substituent. Mechanisms to acount for the observed products of degradation have been suggested and are discussed. Relative thermal stability studies have also been made and compared with results from polystyrene.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/app.1969.070130718
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  • 10
    Digitale Medien
    Digitale Medien
    Thermal degradation of polymers. II further thermogravimetric and differential thermal analysis studies of atactic poly(m-aminostyrene) homopolymers, copolymers, and related polymers (1969)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 401-415 
    Details
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Thermogravimetric and differential thermal analysis have been employed to study the effect on the thermal degradation pattern in static air of the molecular weight of poly(m-aminostyrene) homopolymers and copolymers with styrene. Related substituted styrene polymers and copolymers with styrene have also been studied in order to assess the effect of introduction of amino, substituted amino, and hydroxy groupings into a polystyrene main chain. The effect of these groupings on the thermal stability of the polymers as compared with polystyrene suggests that the inherent antioxidant characteristics of the subtituent grouping plays the major role in stabilization. A molecular weight effect has been shown to be operative for m-aminostyrene, p-N,N-dimethylaminostyrene, and m-hydroxystyrene polymers. This manifests itself in terms of different thermograms rather than by significantly influencing the procedural decomposition temperatures, although a trend is seen.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/app.1969.070130301
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