2021Chemical CommunicationsRequires access

Synthesis of thiophene-fused porphyrin dimers as effective π-extended helical chromophores

Issei Nishimura, Tomohiro Higashino, Hiroshi Imahori

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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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What this paper is about

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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Available 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.

Key concepts: Thiophene, Porphyrin, Chromophore, Photochemistry, Chemistry, Polymer chemistry, Organic chemistry

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