Synthesis of thiophene-fused porphyrin dimers as effective π-extended helical chromophores
Issei Nishimura, Tomohiro Higashino, Hiroshi Imahori
Abstract
Issei Nishimura, Tomohiro Higashino, Hiroshi Imahori
Abstract
We synthesized thiophene-fused porphyrin dimers as effective π-extended helical chromophores. The porphyrin dimers exhibit a red-shifted absorption with the edge extending up to 1100 nm, implying strong electronic communication over the two porphyrin moieties through the thiophene-fused structure. Importantly, their racemic inversion barriers can be modulated by the central metal ions.
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We synthesized thiophene-fused porphyrin dimers as effective π-extended helical chromophores. The porphyrin dimers exhibit a red-shifted absorption with the edge extending up to 1100 nm, implying strong electronic communication over the two porphyrin moieties through the thiophene-fused structure. Importantly, their racemic inversion barriers can be modulated by the central metal ions.
Key concepts: Thiophene, Porphyrin, Chromophore, Photochemistry, Chemistry, Polymer chemistry, Organic chemistry