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Ruthenium catalyzed regioselective copolymerization of acetophenone and α,ω-dienes

Addition of aromaticortho C−H bonds across C−C double bonds of α,ω-dienes

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Summary

This paper reports a novel ruthenium catalyzed regioselective copolymerization reaction between acetophenone and α,ω-dienes such as divinyltetramethyldisiloxane and divinyldimethylsilane which leads respectively to copoly(3,3,5,5-tetramethyl-4-oxa-3,5-disila-1,7-heptanylene/2-acetyl-1,3-phenylene) and copoly(3,3-dimethyl-3-sila-1,5-pentanylene/2-acetyl-1,3-phenylene). This reaction involves the ruthenium catalyzed insertion of the carbon-carbon double bonds of α,ω-dienes into the aromatic C−H bondsortho to the acetyl group of acetophenone. Similar ruthenium catalyzed reactions between acetophenone and alkenes to yield monomericortho alkyl substituted acetophenones have been recently reported.1

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Guo, H., Weber, W.P. Ruthenium catalyzed regioselective copolymerization of acetophenone and α,ω-dienes. Polymer Bulletin 32, 525–528 (1994). https://doi.org/10.1007/BF00973897

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  • DOI: https://doi.org/10.1007/BF00973897

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