55006-58-1Relevant articles and documents
A simple "palladium-free" synthesis of phenyleneethynylene-based molecular materials revisited
Lydon, Donocadh P.,Porres, Laurent,Beeby, Andrew,Marder, Todd B.,Low, Paul J.
, p. 972 - 976 (2007/10/03)
Nucleophilic attack of acetylide anions at the two carbonyl moieties of para-quinones readily affords the corresponding diols. Subsequent reduction with stannous chloride affords a number of useful compounds, including 1,4-bis[(trimethylsilyl)ethynyl]benzene, 1,4-bis[(trimethylsilyl)ethynyl] naphthalene and 9,10-bis[(trimethylsilyl)ethynyl]anthracene. Sequential attack by different acetylide anions followed by reduction provides a useful route to differentially substituted compounds including 1-[(4-nonyloxyphenyl)ethynyl]-4- (phenylethynyl)benzene, a new luminescent liquid-crystalline material. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2005.