Dihydridocarbonyltris(triphenylphosphine)ruthenium catalyzed copolymerization of acetophenone and 1,4-bis((trimethylsilyl)ethynyl)benzene yields a linear copolymer copoly[2-acetyl-1,3- phenylene/α,α‘-bis((trimethylsilyl)methylene)-1,4-xylenylene]. This reaction involves regioselective catalytic addition of the ortho C−H bonds of acetophenone across the C−C triple bonds of 1,4-bis((trimethylsilyl)ethynyl)benzene such that the hydrogen becomes bonded to the carbon which bears the trimethylsilyl group. A similar ruthenium catalyzed reaction between 1,4-bis((trimethylsilyl)ethynyl)benzene and 2-methylacetophenone has been used to prepare α,α‘-1,4-bis-[β-(trimethylsilyl)-2-acetyl-3-methylstyrenyl]benzene, a monomeric compound which possesses the same type of chromophore as the linear polymer. Analogous ruthenium catalyzed reaction of 4-((trimethylsilyl)ethynyl)acetophenone yields a hyperbranched material. All three of these cross-conjugated unsaturated materials have regularly alternating arylene and 1,1-vinylene units. These materials have been characterized by 1 H, 13 C, and 29 Si NMR and by IR, UV, and fluorescence spectroscopy. Polymer properties have been measured by GPC, DSC, and TGA.
No takes yet. Share an insight, caveat, or question.
Londergan et al. (1998) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: