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  • 11
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 187 (1986), S. 1907-1914 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The curing reaction of the new bis(2,3-epoxypropyl) 4,4′-carbonyldi-ω-phthalimidoalkanoates 1a-c was studied with several aromatic diamines 2a-c as curing agents. The process was followed by means of spectrophotometric techniques. The influence of the nature of the curing agent on the reaction rate was examined. The adduct formation yielding first chain extension, is the first step of the reaction, followed by crosslinking, once the gel point has been reached. The products obtained were found to be rather thermostable.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 12
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The substitution reaction of PVC with sodium dimethyldithiocarbamate (NaDC) and sodium azide (NaN3) was performed in cyclohexanone and dimethylformamide at various temperatures. The degree of compositional heterogeneity was estimated and found to be important up to conversions of about 0,5%, but to vanish afterwards. The evolution of unreacted iso, hetero and syndiotactic triads was measured by 13C NMR spectroscopy. For conversions of at least up to 12%, the content of both the isotactic and heterotactic triads was found to decrease, relative to the syndiotactic ones, but at different relative rates depending on the nucleophile. From these results, together with the kinetic ones, it is concluded that the reaction proceeds by a stereoselective mechanism. The results are discussed on the basis of a hypothesis concerning the role of the local triad conformations in PVC that contain the TT isotactic diad conformation. The results enable the selective substitution of PVC with NaDC and NaN3, which may be used as a useful tool to prepare specific graft copolymers based on PVC.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 13
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 191 (1990), S. 281-287 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The molecular species proposed for the initial steps in the cationic polymerization of alkenylfurans were modeled by MNDO theoretically fully optimized structures. It was confirmed that the anomalous reactivity of ring C-5 of the monomers is determined by HOMO electron densitites, whereas calculated proton affinities from the semiempirical heats of formation fail to explain the low temperature experimental behavior of 2-vinylfuran (1c) from the point of view of stability of intermediate species. However, ab initio 4-31G calculations of proton affinities agree with the experimental facts and allow further explanations of the reactivity of furan derivatives in electrophilic media.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 14
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 184 (1983), S. 1189-1211 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A spectroscopic (UV, IR, 1H NMR) study of the cationic polymerisation of 2-vinylfuran (1a) and 2-isopropenylfuran (2a) showed the existence of an important alkylation reaction at C5 which competes with normal propagation. The extent of this competition depends on the monomer used and the polymerisation temperature. A comparison of the spectra of standard polymers (prepared by radical or stereospecific polymerisation) with those of polymers obtained by cationic initiation allowed to assess the extent of alkylation and its regiospecificity at C5 2-Methyl-5-vinylfuran (1b) and 2-methyl-5-isopropenylfuran (2b) were found to undergo cationic polymerisation without any interference from alkylation reactions. Reactions between these four monomers and 2-methylfuran in the presence of typical acidic catalysts gave very high yields of alkylated products and no polymerisation, thus confirming the importance of this electrophilic reaction and its possible application to synthetic uses.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 15
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 1277-1284 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The products resulting from the reaction of PVC with sodium benzenethiolate were degraded to 0,3% at 180°C in the solid state and at 160°C in solution in trichlorobenzene. The polyene distribution of the polymers after degradation was studied by both UV-visible and resonance Raman spectroscopies, as a function of the degree of substitution. The results show that there are two types of behaviour: that of the PVC sample prior to the substitution reaction together with the samples modified up to a definite degree of substitution which depends on the starting isotactic content, and that of samples with higher degrees of substitution. The former group exhibits not only a steady improvement in thermal stability but also a preferential formation of polyenes of 7 - 9 double bonds whose concentration decreases with increasing degree of substitution. Conversely, for the second group of samples the thermal stability decreases with the degree of substitution and no specific absorption bands are observed. On the basis of earlier work on the selective substitution of the isotactic GTTG and heterotactic TTTG triads during the first stage of the reaction, the present results show that the bands at 393, 416, and 437 nm are related to specific polyenes which result from initiation by the above quoted conformations in PVC, a conclusion for which confirmatory evidence was obtained by resonance Raman spectroscopic examination of the samples. There is, therefore, clear evidence for the occurrence of two distinct degradation mechanisms, one involving initiation by the unstable triad conformations and the other via random initiation at stable and normal structures. To this may be added the initiation by defect structures, which have been extensively documented in the literature.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 16
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 188 (1987), S. 2831-2838 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The modification reaction of dextran with butyl isocyanate using 1,4-diaza[2.2.2]bicyclooctane as catalyst was studied. The structure of the resulting polymers was determined by means of IR, 1H and 13C NMR spectroscopy as well as by chemical analysis. A linear dependence of the reaction rate on the concentrations of polymer, butyl isocyanate and catalyst was found. The activation energy was found to be 38,5 kJ/mol (9,2 kcal/mol). The homogeneous hydrolysis in alkaline medium was found to be first order with respect to both the base and the butyl urethane concentrations. The activation energy, obtained for the base catalyzed homogeneous hydrolysis, was 83,7 kJ/mol (20,0 kcal/mol). The heterogeneous hydrolysis of a water insoluble modified dextran (degree of substitution = 0,72) showed that no hydrolysis takes place under the applied conditions.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 17
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The thermally stimulated depolarization currents (TSDC) technique has been used to study molecular motions around the glass transition in three different samples of poly(vinyl chloride) (PVC) varying in the contents of isotactic triads. The α-relaxation mode associated with cooperative molecular motions taking part in glass transition appears to be strongly dependent on tacticity. A secondary relaxation mode α′, different from the β-relaxation, has been detected just below the α-relaxation and at temperatures depending on the content of isotactic triads. Above the glass transition temperature the TSDC curves show a ρ-peak corresponding to the motion of free charges in the material. This process does not seem to be affected by tacticity. The results suggest that specific conformations of isotactic triads play an important role in the motion of chain segments in the polymer.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 18
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Poly(hydroxy ether of Bisphenol-A), so-called Phenoxy resin (structure-based IUPAC name: poly[oxy(2-hydroxytrimethylene)oxy-1,4-phenyleneisopropylidene-1,4-phenylene]), is shown to be miscible with poly(4-vinylpyridine) (P4VPy, poly[1-(4-pyridyl)ethylene]) and poly(2-vinylpyridine) (P2VPy, poly[1-(2-pyridyl)ethylene]) over the entire composition range. Miscibility of the blends is evidenced by their glass transition temperatures being intermediate between the pure polymers for the blends of P4VPy and Phenoxy but being higher than the average for the case of the P2VPy/Phenoxy blends. Hydrogen bonding between the components was detected through infrared spectroscopy, which was also used in the study of mixtures of low-molecular-weight analogues, in order to calculate the free energies of mixing according to the association model of Painter and Coleman.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 19
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 953-962 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Six new acetylene-terminated (AT) oligomers were synthesized by reaction of 3-ethynylbenzoyl chloride and 4-ethynylbenzoyl chloride with three aromatic diamines containing four aromatic rings. The functionalization led quantitatively to AT oligomeric diamides of well defined composition, as confirmed by IR, 1H NMR and 13C NMR spectroscopy. The materials exhibited comparatively high melting points, over 200°C; thus, heating promoted curing before melting or simultaneously with melting, with the only exception of one sample that could be isolated in the amorphous state. Heating at 325°C led to insoluble cured materials, with excellent thermal resistance and glass transition temperatures Tg around 300°C.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 20
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Furfuryl alcohol polymerizes in a suspension of dispersed inorganic solids such as silica in 1,2-dichloroethane using trifluoroacetic acid as initiator. Depending on the experimental conditions the reactions load to (1) agglomeration of particles, (2) composite and soluble polymer formation, (3) composite formation. The chemical structure of the soluble polymers is not regular but the furfurylic sequence is predominant. The polymer grafted on the surface of the solid is a strongly reticulated poly(furfuryl alcohol), which also possesses conjugated double bonds that are involved in an acid-base equilibrium with trifluoroacetic acid.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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