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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 74 (1962), S. 79-79 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    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: Polyspiroacetal polymers and copolymers derived from pentaerythritol, and glutaraldehyde were prepared and examined for physical properties. Elemental and infrared analyses support the polyspiroacetal structure. X-ray analysis indicates a range of 20-40% crystallinity. Dipentaerythritol was observed to influence in varying degrees the crystallinity, the solubility, and the optimum range of film curing conditions. Resins with more than 25% dipentaerythritol always crosslinked during polymerization. In addition, the variables influencing such resin properties as molecular weight and gelation were examined. Films crosslinked with pyromellitic dianhydride exhibited good flexibility and tensile strength. Moreover, their oxidative thermal stability was only slightly less than that of crosslinked poly(ethylene terephthalate).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of the compounds C12F8M2 (M = S, Se), (I), C12F8M (M = S, Se, Te), (II) and C12F8SX2 (X = Br, I), (III), have been measured. Results indicate that sulfur-carbon bonds are more stable under electron bombardment than either selenium-carbon or tellurium-carbon bonds. Numerous metastable-supported transitions are evident, which are incorporated into comprehensive fragmentation schemes for these compounds. Many metastable transitions, not previously reported, were observed for the fluorocarbon fragments and a fragmentation scheme is reported.The bromine and iodine-containing compounds behave remarkably like the heterocyclic systems, I and II, presumably due to initial loss of Br2 or I2 to form a ring system of type II.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The metastable ion supported fragmentations and fluorine transfer rearrangements of a series of fluoroaromatic heterocyclic derivatives of silicon, germanium and tin are reported. Of particular interest is the unique loss of neutral SiF4 from the parent ion of (C12F8)Si yielding the [C24F12]+· ion. These and similar rearrangements are discussed and structures are proposed for some of the ions observed. The general case of cyclic rearrangement intermediates prior to the loss of neutral metal fluorides from perfluoroaromatic derivatives is discussed. Losses of neutral metal fluorides from the parent ions appear to involve a species with increased co-ordination number about the central atom as an intermediate. In addition to (C12F8)2M, the following compound types were studied: (C6H5)2Ge(C12F8), (C12F8S)2M and R4Sn2(C6F4)2 (where M = a Group IV metal and R = CH3 or C6H5).
    Additional Material: 5 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 3263-3299 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A number of phenyl polyesters have been synthesized to furnish molecules whose backbones rearrange under ultraviolet irradiation to an o-hydroxybenzophenone structure. This photochemical Fries rearrangement produces ultraviolet opacity in the irradiated film while maintaining visual transparency. Thin coatings of these polyesters completely protect substrates ordinarily sensitive to ultraviolet light. Spectroscopic analysis of various rearranged films and coatings clearly shows that the o-hydroxybenzophenone polymer formed is concentrated at the irradiated surface of the original polyester coating as a “skin”. Such a skin, formed in situ during the irradiation, functions to protect both the original polyester coating as well as the coated substrate from degradation by ultraviolet irradiation. Furthermore, a significant “healing” mechanism appears inherent in these coatings, for as the exposed skin ultimately degrades under extended ultraviolet irradiation, more of the underlying polyester layer apparently rearranges to compensate for the loss. Thus the clear coating functions both as a protective skin and a rearrangeable reservoir. Modified structures of the polyesters have been prepared which possess, in addition to their protective film properties, a useful solubility spectrum and a good solution shelf life.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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