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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 95 (1991), S. 6341-6346 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 30 (1991), S. 440-447 
    ISSN: 1520-5045
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Journal of sol gel science and technology 9 (1997), S. 251-263 
    ISSN: 1573-4846
    Schlagwort(e): sol-gel process ; Raman spectroscopy ; formic acid-alkoxide route ; organically modified silica gels
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract For precursor mixtures containing tetraethoxysilane (TEOS) and phenyltriethoxysilane (PhTREOS), time of gelation can be reduced by up to two orders of magnitude depending on reaction conditions employed when reacting the silicon alkoxide mixture with formic acid instead of water. Results indicate that time of gelation depends on the amount of PhTREOS in the precursor mixture. Within the range of concentrations investigated, an exponential law describes best the dependence of reduced time of gelation on the molar fraction of PhTREOS. Therefore, we conclude that the phenyl ring acts as a steric hindrance to network formation. Raman spectroscopy is used to characterize the reaction between the alkoxide mixture and formic acid. During the acidolysis reaction, ethanol is formed as an intermediate. A preliminary reaction scheme is proposed to account for the time dependence of species involved. Furthermore, Raman spectroscopy is successfully employed to monitor the effects of post-gelation thermal treatment of the gel samples. The effects observed are interpreted with a model of a phenyl ring trapped in a siloxane cage.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Journal of sol gel science and technology 9 (1997), S. 251-263 
    ISSN: 1573-4846
    Schlagwort(e): sol-gel process ; Raman spectroscopy ; formic acid-alkoxide route ; organically modified silica gels
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract For precursor mixtures containing tetraethoxysilane (TEOS) and phenyltriethoxysilane (PhTREOS), time of gelation can be reduced by up to two orders of magnitude depending on reaction conditions employed when reacting the silicon alkoxide mixture with formic acid instead of water. Results indicate that time of gelation depends on the amount of PhTREOS in the precursor mixture. Within the range of concentrations investigated, an exponential law describes best the dependence of reduced time of gelation on the molar fraction of PhTREOS. Therefore, we conclude that the phenyl ring acts as a steric hindrance to network formation. Raman spectroscopy is used to characterize the reaction between the alkoxide mixture and formic acid. During the acidolysis reaction, ethanol is formed as an intermediate. A preliminary reaction scheme is proposed to account for the time dependence of species involved. Furthermore, Raman spectroscopy is successfully employed to monitor the effects of post-gelation thermal treatment of the gel samples. The effects observed are interpreted with a model of a phenyl ring trapped in a siloxane cage.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 61 (1978), S. 1193-1199 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Ab initio SCF and CI calculations on the cationic and neutral complexes of formaldehyde and lithium are reported. For the cationic complex CH2O/Li+, the stabilization energy of 41.7 kcal/mol obtained from the SCF calculation increases to 51.6 kcal/mol if a configuration interaction is introduced. For the neutral complex CH2O-/Li+, the C2v-conformer of the 2A1-state with the equilibrium bond distances of d(C—O) = 1.23 Å and d (O—Li) = 1.90 Å is calculated to be more stable than the 2B1-state with d (C—O) = 1.34 Å, and d (O—Li) = 1.65 Å. Charge transfer and polarization effects upon complex formation are discussed.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 3385-3391 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In the photochemical decomposition of triazene R—N=N—NR1R2 in CH3CN solutions, where R was (3-HOOC—, di-HOOC—, 4-HOOC—, 4-CN—)phenyl and R1, R2 were —CH3, —CH2H5, —CH(CH3)2, —CH2CH2OH, the corresponding phenyl-substituted radicals were identified as 5,5-dimethyl-1-pyrroline N-oxide (DMPO) or (CH3)3CNO adducts. The reaction is described by a first-order kinetics with a half lifetime of 7 s. If R was di-3,5-CON3-C6H3—, a nitrogen-centred radical was found on radiation in the solid state as well as in CH3CN solution with DMPO as spin trap.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    ISSN: 0930-7516
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: Two vanadia/titania catalysts, containing 1 and 8 wt% vanadia on anatase, have been investigated for the selective oxidation of o-xylene to phthalic anhydride. In a comparative study, activity and selectivity in o-xylene oxidation were measured using an integral reactor and a reactor with external product recirculation, with the objective of studying the influence of backmixing in the latter on the reaction behaviour. Adsorbed surface species were investigated by means of in-situ diffuse reflectance FT-IR spectroscopy, using an environmental chamber which corresponds to an integral reactor. No difference in activity and selectivity in o-xylene oxidation was observed between the two catalysts. FT-IR studies showed adsorbed o-xylene, benzoate and a high concentration of phthalic anhydride on the surface of both catalysts. o-Xylene oxidation follows a sequential reaction path, with o-tolualdehyde as the first intermediate and phthalide, phthalic anhydride and maleic anhydride as sequential products. No evidence was found for a direct oxidation-path of o-xylene to phthalic anhydride. Total oxidation products CO and CO2 are formed by direct oxidation of the o-xylene and by oxidation of the reaction products. Due to greatly reduced concentration and temperature gradients, the recycle reactor proved to be highly suitable for studying the extremely exothermic oxidation of o-xylene.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 196 (1995), S. 739-749 
    ISSN: 1022-1352
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The synthesis of novel triazeno-group containing photopolymers is described including their characterization by spectroscopic methods, differential scanning calorimetry, and thermogravimetric analysis. Triazene polymers synthesized by a polycondensation reaction between a bisdizaonium salt and a bifunctional secondary amine are well soluble in usual organic solvents. Transparent, light yellow films of these photopolymers may be produced by simple spin-coating and solution-casting techniques. The effect of polymer structural elements on the photolytic decomposition is studied. Depending on the structure of the polymer, thermolysis proceeds either via a one-step or two-step mechanism.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 196 (1995), S. 751-761 
    ISSN: 1022-1352
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The depolymerization of a triazeno-group containing photopolymer, poly[oxy-1,4-phenyleneazo(methylimino)hexamethylene(methylimino)azo-1,4-phenylene], is investigated in a tetrahydrofuran (THF) solution. Irradiation of the material leads to a clean decomposition of the photolabile polymer, as monitored by UV spectroscopy and gel-permeation chromatography (GPC). As compared to the photolysis in THF solution, the light-induced decomposition rate of a polymer in a polymer film is shown to be much slower. The highly photosensitive triazeno group also decomposes thermally at temperatures above approx. 220°C. The kinetics of thermal degradation of the polymer in substance was investigated at a temperature of 256°C, and monitored by GPC measurements. During this decomposition, one first observes the development of higher molar-mass fractions, which result from grafting reactions of primary radicals. Upon further thermolysis the triazene polymer is completely degraded to low-molar-mass products. The volatile decomposition products were identified by gas chromatography/mass spectrometry (GC/MS) analysis. The protolytic decomposition, which represents the retrosynthesis of the triazene polymer, was studied in a 9:1 mixture of tetrahydrofuran and an aqueous citrate buffer solution. Although the decomposition rate in this solvent mixture is slow, as compared to the depolymerization in diluted hydrochloric acid, a clean decomposition of the triazene polymer is obtained.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    ISSN: 0935-9648
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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