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  • 1
    Electronic Resource
    Electronic Resource
    Susceptibility of tenascin to degradation by matrix metalloproteinases and serine proteinases
    Amsterdam : Elsevier
    FEBS Letters 352 (1994), S. 216-218 
    Details
    ISSN: 0014-5793
    Keywords: Matrix metalloproteinase ; Serine proteinase ; Tenascin
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/0014-5793(94)00960-0
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Synthesis of novel organic oligomers containing Si—H bonds (1993)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2617-2631 
    Details
    ISSN: 0887-624X
    Keywords: SiH-containing oligomers ; partial hydrosilylation ; Pt-catalyzed ; hydrocyclotetrasiloxane ; allyloxy (or allyl carbonate) end-blocked oligomers ; NMR analysis ; storage stability ; coordinating compounds ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several organic oligomers (Mw = 103-104 order) containing Si=H bonds of the general formula 1 have been successfully synthesized by platinum-catalyzed partial hydrosilylation reaction of an allyloxy (or an allyl carbonate) end-blocked linear organic oligomer 2 with 2,4,6,8-tetramethylcyclotetrasiloxane, [CH3(H)SiO]4 (3) (hereafter called hydrocyclotetrasiloxane). 1H-NMR spectroscopy confirmed the introduction of hydrocyclotetrasiloxane moiety into the oligomers through Si—C linkage by hydrosilylation reaction. 13C-NMR analysis revealed that the cyclic structure of the starting hydrocyclotetrasiloxane 3 was retained intact in product 1. As the precursor for 1, allyloxy (or allyl carbonate) end-blocked oligomers 2 could be prepared from hydroxyl-terminated oligomers 4. The storage stability of product 1 was significantly influenced by the platinum catalyst still remaining in it. The poor stability was improved by decreasing the amount of the platinum catalyst and/or by adding coordinating compounds. As a result, an excellent stability of product 1 was obtained. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1993.080311023
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  • 3
    Electronic Resource
    Electronic Resource
    Curing system involving SiH-containing organic oligomers (1993)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 825-833 
    Details
    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: We describe here the preparation and properties of a novel curing system, which has been derived from an SiH-containing organic oligomer 1 and an allyloxy end-blocked organic oligomer 2. The composition of these oligomers could be crosslinked via a platinum-catalyzed hydrosilylation reaction, that is, the addition reaction of the SiH bonds of 1 to the allyl functionality of 2, above 100°C, yields a rubbery material in a short period of time. The compatibility of the SiH-containing oligomer 1 with the allyloxy end-blocked oligomer 2 was governed by the oligomer main chain employed. Hence the SiH-containing oligomer 1 was completely miscible with 2, having the same main chain and, thus, the system yielded a homogeneously cured material. The poly(propylene oxide) curing system 1a/2a was systematically investigated in detail to manifest its curing behavior and crosslink structure. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1993.070500509
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  • 4
    Electronic Resource
    Electronic Resource
    XPS and SERS Studies of Cell Adhesion-controlled Polymer Modified by Ion Implantation (1996)
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 252-256 
    Details
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: X-ray photoelectron spectroscopy (XPS) of Ne ion-bombarded polymer has been carried out in order to examine the cause of HeLa cell adhesion control on polymers. Substrates used were polystyrene (PS) and oxygen plasma-treated polystyrene (PS-O). Neon bombardments into the patterned region of PS and PS-O were performed at an energy of 150 keV with fluences of 1×1014 and 1×1015 ions cm-2. The surface chemical bonding states were investigated by XPS. In HeLa cell adhesion measurements, the Ne-bombarded region of PS with a fluence of 1×1015 ions cm-2 exhibits higher adhesion and spreading of HeLa cells than the unbombarded region. On the contrary, it is found that the Ne-bombarded region of PS-O inhibits HeLa cell adhesion. The XPS results show that Ne bombardment to PS or PS-O destroys the original chemical bonds and consequently produces new functional groups. It is considered that the drastic change of surface chemical bonding states from the pristine states induced by Ne bombardment leads to a clear distinction between increasing and inhibiting HeLa cell adhesion.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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