Abstract
Planar, methylene-bridged quinque- and septiphenyl oligomers were synthesized as soluble, hitherto unknown compounds. The series of homologous and planar ladder-type oligophenyls (ter-, quinque-, septiphenyl) was characterized especially with respect to their optical properties (absorption and emission) as function of increasing chain length, and compared to the corresponding ladder-type polyphenylene. An effective conjugation length of about 12 benzene rings was determined within this series of planar oligo- and polyphenylenes.
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CITATION STYLE
Grimme, J., & Scherf, U. (1996). Planar para-phenylene oligomers. Macromolecular Chemistry and Physics, 197(7), 2297–2304. https://doi.org/10.1002/macp.1996.021970720
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