The synthesis of poly(paraphenylene)s (PPPs) bearing sterically π-congested 2,2′,6,6′-tetraphenyl-1,1′-biphenyl (1) units has been achieved for the first time. By enhancing the synthesis of 1, followed by its polymerization, we were able to compare the photophysical properties of the oligomeric and polymeric fractions with non-crowded PPPs. This revealed significant π-orbital interactions along the paraphenylene backbone of the π-congested systems together with through-space conjugation among the π-orbitals of the stacked peripheral phenyl rings, resulting in an increased effective conjugation length and a remarkable bathochromic shift in absorption.
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