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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