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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 681-693 
    ISSN: 0268-2605
    Keywords: ceramics ; preceramic polymers ; SiNCB composites ; boron nitride ; boron ; silicon ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Our recent work directed at the design, synthesis, characterization and applications of new types of polyborazylene and polyborosilazane polymers is reviewed with a focus on the use of these polymers as processable precursors to BN and SiNCB composites. A design strategy based on the controlled functionalization of preformed polymers with pendant groups of suitable compositions and crosslinking properties has been employed to yield second-generation dipentylamine-polyborazylene (DPA) and pinacolborane-hydridopolysilazane (PIN-HPZ) polymers, which, unlike the parent polyborazylene (PB) and the borazine-hydridopolysilazane (B-HPZ) polymers, are stable as melts and can be easily melt-spun into polymer fibers. Subsequent pyrolyses of these polymer fibers then provide excellent routes to BN and SiNCB ceramic fibers. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 11 (1972), S. 1773-1778 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of poly[(S)-thiazolidine-4-carboxylic acid] is described. The polymer is obtained by the polymerization of the N-carboxyanhydride of (S)-thiazolidine-4-carboxylic acid in pyridine or nitrobenzene using triethylamine as an initiator. The amino acid is prepared by the condensation of cysteine and formaldehyde. N-Acetyl-(S)-thiazolidine-4-carboxylic acid methyl ester is also prepared as a model compound by standard acetylation and esterification reactions.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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