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Siloxane−Triarylamine Hybrids: Discrete Room...
Journal article

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

Abstract

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 (19)F NMR.

Authors

Kamino BA; Grande JB; Brook MA; Bender TP

Journal

Organic Letters, Vol. 13, No. 1, pp. 154–157

Publisher

American Chemical Society (ACS)

Publication Date

January 7, 2011

DOI

10.1021/ol102607v

ISSN

1523-7060

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