Siloxane−Triarylamine Hybrids: Discrete Room Temperature Liquid Triarylamines via the Piers−Rubinsztajn Reaction

A series of room temperature liquid siloxane−triarylamine hybrids were synthesized using the Piers−Rubinsztajn reaction. These materials displayed well behaved electrochemical oxidation and low T g’s and were free-flowing liquids. The interaction between the Lewis acidic tris(pentafluorophenyl)boran...

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Veröffentlicht in:Organic letters 2011-01, Vol.13 (1), p.154-157
Hauptverfasser: Kamino, Brett A, Grande, John B, Brook, Michael A, Bender, Timothy P
Format: Artikel
Sprache:eng
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Zusammenfassung:A series of room temperature liquid siloxane−triarylamine hybrids were synthesized using the Piers−Rubinsztajn reaction. These materials displayed well behaved electrochemical oxidation and low T g’s and were free-flowing liquids. The interaction between the Lewis acidic tris(pentafluorophenyl)borane catalyst and the Lewis basic starting triarylamine substrate was also investigated by steady state UV−vis spectroscopy and 19F NMR.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol102607v