Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1327540 | Journal of Organometallic Chemistry | 2006 | 6 Pages |
Reactions of (bromophenylethenyl)diethoxysilanes with magnesium in THF gave poly[(ethoxysilylene)phenylenevinylene]s. The ethoxy group of the polymers could be readily replaced with other substituents by treating them with nucleophiles. Optical properties of the resulting poly(silylenephenylenevinylene)s were examined with respect to their UV absorption and emission spectra. Of those, pyrenylethynyl-substituted one exhibited energy transfer from the backbone to the substituent in the photo-excited state.
Graphical abstractSynthesis of poly[(ethoxysilylene)phenylenevinylene]s, followed by their reactions with nucleophiles provides a route to variously substituted poly(silylenephenylenevinylene)s. Of the resulting polymers, pyrenylethynyl-substituted one exhibited energy transfer from the backbone to the substituent in the photo-excited state.Figure optionsDownload full-size imageDownload as PowerPoint slide