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Issue 18, 2008
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Solid state structures and photophysical properties of (trimethylsilyl)methyl-substituted anthracenes and pyrenes

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Abstract

(Trimethylsilyl)methyl groups incorporated at 9- and 9,10-positions of anthracenes and at 1,3,6,8-positions of pyrenes were found to orient perpendicular to the aromatic frameworks in their crystals and induce red-shift of UV absorption and fluorescence spectra and enhancement of fluorescence quantum yields as compared with the parent hydrocarbons.

Graphical abstract: Solid state structures and photophysical properties of (trimethylsilyl)methyl-substituted anthracenes and pyrenes

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Supplementary files

Article information


Submitted
31 Oct 2007
Accepted
07 Feb 2008
First published
27 Feb 2008

Chem. Commun., 2008, 2134-2136
Article type
Communication

Solid state structures and photophysical properties of (trimethylsilyl)methyl-substituted anthracenes and pyrenes

M. Shimizu, H. Tatsumi, K. Mochida and T. Hiyama, Chem. Commun., 2008, 2134
DOI: 10.1039/B716770A

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