Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9776222 | Synthetic Metals | 2005 | 4 Pages |
Abstract
We have investigated the chemical and electrochemical polymerizations of polyether-functionalized 3'-styrylterthiophene monomers. A comparison of the UV/VIS/NIR spectra of the polymerization products formed from four of these styrylterthiophenes that were either unsubstituted or incorporated decyloxy groups at the 4 and 4”-positions, provides evidence for the formation of significantly longer-chain materials from the decyloxy-substituted compounds.
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Biomaterials
Authors
D.K. Grant, D.L. Officer,