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Synthesis and Ionochromic Effect of Hyperbranched and Linear Poly(thienylene−phenylene)s
A novel hyperbranched poly(thienylene−phenylene) is synthesized, which is compared with a poly(2,3-thienylene−phenylene) and a poly(2,5-thienylene−phenylene). The hyperbranched polymer has much greater solubility in organic solvents than its isomeric linear polymers. A pronounced ionochromic effect...
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Published in: | Macromolecules 2003-04, Vol.36 (8), p.2689-2694 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A novel hyperbranched poly(thienylene−phenylene) is synthesized, which is compared with a poly(2,3-thienylene−phenylene) and a poly(2,5-thienylene−phenylene). The hyperbranched polymer has much greater solubility in organic solvents than its isomeric linear polymers. A pronounced ionochromic effect is observed for the poly(2,5-thienylene−phenylene) in the presence of LiBF4. This polymer shows a large red shift in its UV−vis spectrum when treated with the metal salt solution. The ionochromic effect is also ion selective. However, both the hyperbranched polymer and the poly(2,3-thienylene−phenylene) show almost no such ionochromic effect probably because of the ortho-substituted thiophene units in their structure. The hyperbranched polymer and the poly(2,5-thienylene−phenylene) are found to be green light emitters and the poly(2,3-thienylene−phenylene) a blue light emitter. These materials are potentially useful for electroluminescence and photovoltaics. |
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ISSN: | 0024-9297 1520-5835 |
DOI: | 10.1021/ma025650x |