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  • 1
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 753-771 
    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: The polymerization of β-propiolactone (βPL) by sodium acetate catalyst has been investigated. The polymerization behavior with monomer purified with calcium chloride was found to be a little different from that previously reported for this monomer. That is, poly-β-propiolactone (PβPL) obtained from βPL dried with CaCl2 has a higher degree of polymerization than that obtained from conventionally treated βPL, and its infrared spectrum shows type II configuration, which differs from that reported in previous papers. Some chain transfer reaction is observed even for the polymerization of the CaCl2-dried βPL; however, this is less important in toluene. The electronegativity of the anion or cation in catalyst greatly influences the rate of polymerization.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 2421-2439 
    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: Acetic acid, toluenesulfonic acid, and their salts are used as four representative ionic catalysts for polymerization of β-propiolactone (βPL). They are classified as follows: sodium acetate is an anionic catalyst, acetic acid is a neutral one having more covalent character, sodium toluene sulfonate is a neutral one having more ionic character, toluenesulfonic acid is a cationic one. The neutral catalyst having more covalent nature is hardly dissociated, and therefore the rate of polymerization is quite small; however, dissociated ions consist of a higher neucleophilic anion and a higher electrophilic cation. On the contrary, the neutral catalyst having an ionic bond dissociates more easily, but the formed ions consist of the less reactive anion and cation. Therefore, it is of interest whether β-propiolactone is polymerized by a cationic mechanism or an anionic mechanism by these catalysts. The mechanisms of polymerizations of βPL by these neutral catalysts were studied on the basis of the different behaviors of polymerizations by the four catalysts described above. In the cationic polymerization by toluenesulfonic acid, the rate of polymerization was high, but the conversion reaches a low, limited value. In the anionic polymerization by sodium acetate, the rate of polymerization was high and the degree of polymerization of polymer was the highest. Acetic acid has the lowest catalyst activity and the degree of polymerization is also very small. It was found that the polymerization by sodium p-toluenesulfonate was accelerated in the presence of acrylic acid produced from βPL by hydrogen-transfer reaction.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 4
    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: β-Propiolactone (βPL) was graft-copolymerized onto styrene-divinylbenzene copolymers containing various carboxylates or sulfonates, composed of anions and cations having different electronegativities. In parallel, the mechanism of polymerizations of βPL by relatively neutral catalysts was studied in comparison with the behaviors of graft copolymerizations. In the graft copolymerization onto the trunk polymer containing various carboxylates, a lower electronegativity of countercation favors a higher anionic polymerization activity and the order of rate of polymerization coincides with that of anionic activities of catalysts. On the other hand, in the case of trunk polymer containing sulfonates, a higher electronegativity of countercation favors a cationic polymerization activity, and the order of rate of polymerization coincides with that of cationic activity of catalyst. The order of grafting efficiency at fixed total conversion coincides almost with that of anionic activity. The comparatively higher grafting efficiency in the grafting onto trunk polymer containing carboxylic acid might support an anionic graft copolymerization mechanism by carboxyl anion. The two following mechanisms were proposed for the initiation of the polymerization by the trunk polymer containing sodium sulfonate, in which acrylic acid is transformed from βPL.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 5
    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: It was pointed out in previous papers that both cationic and anionic polymerization might be involved simultaneously in grafting onto trunk polymers containing —COOH or —SO3Na. The graft copolymerization of β-Propiolactone (βPL)-N-vinylcarbazole (NVCZ) onto styrene-divinylbenzene copolymers containing carboxylic acid, sulfonic acid, and their salts was carried out in order to distinguish between the polymers produced by anionic and cationic mechanisms. The polymer obtained by the polymerization of βPL-NVCZ with BF3·OEt2, a typical cationic catalyst, consisted mainly of NVCZ units, but the polymer obtained with BuLi, a typical anionic catalyst, consisted mainly of βPL units. In the graft copolymerization of NVCZ-βPL onto trunk polymer containing —COOH, the NVCZ contents of the branch polymer and the tolueneinsoluble fraction were estimated to be ca. 50 mole-%; therefore these polymers were produced by both cationic and anionic mechanisms. In the case of graft copolymerization onto the trunk polymer containing SO3Na, it was found that both cationic and anionic polymerization also occurred simultaneously.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 773-790 
    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: Polyacrylonitrile-β-propiolactone (βPL) graft copolymer was synthesized by means of ionic polymerization, in which polymerization of βPL was initiated by polyacrylonitrile containing a small amount of some reactive groups such as —COOK, —COONa, —COOLi, and —COOH. Lower electronegativity of the countercation favored higher total conversion and higher grafting percentage. The grafting percentage increased with the reaction time and concentration of reactive groups in the trunk polymer, but grafting efficiency varied very little under these conditions. In the bulk polymerization at 60°C., grafting efficiency was about 60%, but in the solution polymerization in toluene or dioxane, grafting efficiency was higher than in bulk or nitrobenzene.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 791-810 
    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: Polyacrylonitrile (PAN)-β-propiolactone (βPL) graft copolymer was synthesized by means of the ionic polymerization of βPL in the presence of polyacrylonitrile containing diketene units by using basic catalysts. A graft copolymer was produced by the copolymerization of βPL with the lactone ring in the trunk polymer. In this graft copolymerization method, the grafting efficiency was low. However, grafting efficiency increased with the mole ratio of polymeric lactone to βPL; also higher molecular weight of PβPL favored higher grafting efficiency. The reactivity ratio of polymeric lactone to βPL was estimated to be in the range of 0.1-0.3.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 8
    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: The graft copolymerization of β-propiolactone (βPL) onto the various trunk polymers containing polar substituents such as pyridine, amide, sulfonyl chloride, and carboxylic acid anhydride groups was carried out. In the grafting onto the basic trunk polymer containing 4-vinylpyriding units, two kinds of grafting mechanism are supposed. In the case of rigorously dried trunk polymer, the polymerization is initiated by betaine and proceeds with higher grafting efficiency. Another is initiated by pyridinium hydroxide and proceeds with lower grafting efficiency. Another is initiated by pyridinium hydroxide and proceeds with lower grafting efficiency in the presence of some amount of water. With acidic trunk polymer containing sulfonyl chloride groups, no graft copolymer was produced. The grafting efficiency of βPL onto the amphoteric trunk polymer containing acrylamide units was found to be between those of basic and acidic trunk polymer. In addition, the grafting by means of ionic copolymerization of βPL with maleic anhydride units contained in trunk polymer proceeded with very high grafting efficiency.
    Additional Material: 6 Ill.
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  • 9
    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: The polymerization of β-propiolactone (βPL) induced by radiation and by radical catalysts, the influences of radical inhibitors and electron acceptors on this polymerization, and graft copolymerization were studied. It was found that βPL was polymerized by benzoyl peroxide in the presence of electron acceptors such as maleic anhydride and acrylonitrile. This polymerization method was applied to graft copolymerization. The electron donative trunk polymer containing ether groups was heated with benzoyl peroxide or was irradiated by γ-rays from Co60 in the presence of maleic anhydride as the electron acceptor. βPL was added subsequently to form the graft copolymer.
    Additional Material: 5 Ill.
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  • 10
    Publication Date: 2020-04-16
    Description: Replication factor C (RFC), a heteropentamer of RFC1-5, loads PCNA onto DNA during replication and repair. Once DNA synthesis has ceased, PCNA must be unloaded. Recent findings assign the uloader role primarily to an RFC-like (RLC) complex, in which the largest RFC subunit, RFC1, has been replaced with ATAD5 (ELG1 in Saccharomyces cerevisiae). ATAD5-RLC appears to be indispensable, given that Atad5 knock-out leads to embryonic lethality. In order to learn how the retention of PCNA on DNA might interfere with normal DNA metabolism, we studied the response of ATAD5-depleted cells to several genotoxic agents. We show that ATAD5 deficiency leads to hypersensitivity to methyl methanesulphonate (MMS), camptothecin (CPT) and mitomycin C (MMC), agents that hinder the progression of replication forks. We further show that ATAD5-depleted cells are sensitive to poly(ADP)ribose polymerase (PARP) inhibitors and that the processing of spontaneous oxidative DNA damage contributes towards this sensitivity. We posit that PCNA molecules trapped on DNA interfere with the correct metabolism of arrested replication forks, phenotype reminiscent of defective homologous recombination (HR). As Atad5 heterozygous mice are cancer-prone and as ATAD5 mutations have been identified in breast and endometrial cancers, our finding may open a path towards the therapy of these tumours.
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
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