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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 3361-3370 
    ISSN: 0887-624X
    Keywords: polysilylene ; polysilane ; Langmuir-Blodget ; phenol ; thin film ; orientation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polysilylenes with a phenol group directly bonded to the main chain Si atom were prepared by polymerizing dichlorosilane monomers bearing phenol groups protected by t-butyldimethylsilyl ether, followed by deprotecting the silyl ether. These amphiphilic polysilanes were applied to provide oriented thin films by the Langmuir-Blodgett technique. Stable monolayers were not obtained for polysilylenes having only alkyl and aryl substituents. However, all the polysilylenes with phenol moieties provided monolayers on a water surface. These polysilylene monolayers were transferred to hydrophobic substrates by applying the Langmuir-Blodgett technique. Among these polysilylenes, only poly(n-butyl-3-hydroxyphenylsilylene) provided multilayers in which the Si—Si main chains oriented in the dipping direction. The orientation was determined by polarized UV absorption. The orientation ratio reached 0.45. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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