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  • Digitale Medien  (18)
  • Physics  (16)
  • Phthalocyanines  (2)
  • 1
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Journal of Photochemistry and Photobiology B: Biology 16 (1992), S. 73-81 
    ISSN: 1011-1344
    Schlagwort(e): Phthalocyanines ; photosensitization ; singlet oxygen ; solvent deuteration ; triplet lifetime.
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Biologie , Chemie und Pharmazie , Medizin
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Journal of Photochemistry and Photobiology B: Biology 9 (1991), S. 87-95 
    ISSN: 1011-1344
    Schlagwort(e): Phthalocyanines ; photodynamic therapy. ; photosensitizers ; time-correlated single-photon counting
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Biologie , Chemie und Pharmazie , Medizin
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1499-1505 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: An apparatus is described which enables the rapid recording of time-resolved emission spectra on a nanosecond time scale. The instrument permits detailed study of the time-dependent photo-physical processes occurring in many polymer systems. The technique has been used to investigate the kinetics of excimer formation in methylene chloride solutions of polystyrene and poly(1-vinyl-naphthalene). Unambiguous evidence for excimer dissociation is observed in poly(1-vinylnaphthalene) but the process appears unimportant in solutions of polystyrene.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 1137-1150 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 4-Aminophthalic acid has been polymerized in almost quantitative yield to low molecular weight polymer by electrochemical initiation at a platinum anode. Systems involving the acid, amine salt, and the ammonium salt have been explored; the acid and/or the amine salt of the acid provides the best means of obtaining polymer. Maximum molecular weight is attained in a very short time at low current densities (∼2 hr at 50 mA). Thermogravimetric data indicate a temperature stability comparable to polyamide-imide polymers (400°C). Long reaction times and high current densities decrease molecular weight and polymer yield.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1411-1418 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The electroinitiated polymerizations of styrene, 2-vinylnaphthalene, and 9-vinylanthracene were compared in sulfolane and acetone solvents in the presence of ZnCl2. The relative orders of polymerization rates and polymerization efficiencies, in both solvents, were 9-vinylanthracene 〉 2-vinylnaphthalene 〉 styrene, with faster rates and higher efficiencies occurring in sulfolane. Data obtained from viscosity and gel permeation chromatography (GPC) studies indicate that the molecular weights of the polymers produced in these systems are extremely low, 〈5000. Chemical composition and infrared (IR) spectral data suggest that abnormal transfer reactions (possibly from solvent) may be occurring in the electroinitiated 9-vinylanthracene polymerizations. The polymerization mechanism appears to be cationic in these monomer-solvent systems with ZnCl2.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 1151-1156 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The electrochemical polymerization of the amino phthalic acid series has been extended to the following derivatives: 4-(4′-aminobenzamido), 4-(2′-aminobenzoyl), and 4-(3′-aminobenzoyl)phthalic acid. Reactions were performed in both dimethylacetamide and ethanol. Both systems produced a film deposit at the anode which was identified as the amide acid of the starting material. Conversion by heat to the imide produced a brittle coating. Inherent viscosity measurements indicate that only low molecular weight material was formed.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 2673-2684 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The zinc chloride-catalyzed polymerization of 2-vinylnaphthalene (VN) with both photoinitiation and electronitiation methods was examined. Good yields were obtained with both methods, the electroinitiated process being somewhat faster. The mechanism for polymerization initiation was investigated through a detailed comparison of the kinetics. Both initiation methods show a similar response to increasing input energy and to change in salt to monomer mole ratio. Both methods indicate formation of a ZnCl2-(2-VN)2 complex as intermediate with the formation of the species being rate-determining. These results, together with other similar investigations, are then used to deduce a mechanism that involves the formation of an electronically excited donor-acceptor complex. It is argued that in certain salt-stabilized, electron-delocalized, aromatic systems, such excitation is possible in electroinitiation.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1711-1720 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The quenching of the triplet states of several model αβ-unsaturated ketones and that produced by thermal oxidation of polybutadiene by the triplet quencher cyclooctadiene at low temperatures has been studied by quantum yield and phosphorescence decay-time methods. Both the Perrin and Inokuti-Hirayama relationships were tested and a typical exchange interaction distance for half-quenching of R0 = 12 ± 1 Å was obtained for both models on all compounds studied.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1867-1879 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The electroinitiated copolymerization of styrene and diethyl fumarate in methanol solvent with zinc bromide as electrolyte has been investigated at high current strengths (200-500 mA). Unlike the copolymerization behavior observed at lower current strengths (〈 200 mA), it is found that the cathodically produced copolymers deviate from a 1:1 composition and show a significant deficiency in styrene. The copolymer products can be separated into two well-defined fractions: a toluene-soluble fraction (normal copolymer) and a toluene-insoluble one (styrene-deficient copolymer). These deviations in copolymer composition from a 1:1 monomer ratio are attributed to the occurrence of cathodically induced electroreductive hydrolysis side reactions with diethyl fumarate leading to the formation of carboxylate or acid salt species. Reaction of these hydrolyzed species with diethyl fumarate results in the formation of fumarate-rich copolymers.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1193-1202 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: With the aid of VPC and NMR, the electroinitiated polymerization of phenol or p-tert-butyl phenol with formaldehyde in the presence of basic electrolytes has been investigated over a range of current densities. Results from an electroinitiation study were contrasted with base-catalyzed thermal polymerizations and, except for yield, found to be essentially invariant. GPC of the electroinitiated and thermally polymerized resins indicates similar results with low molecular weight species of relatively narrow molecular weight distribution being the principal products. An electroinitiation mechanism, in agreement with the mechanism for base-catalyzed thermal polymerization is proposed to describe these experimental results.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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