News Release

Synthesis of peripherally annulated phenanthroporphyrins

A new approach for peripheral annelation of porphyrinoid

Peer-Reviewed Publication

Ehime University

Stepwise synthesis of unusual phenanthrene-fused porphyrins

image: Unusual phenanthrene-fused porphyrins were successfully synthesized via thermal conversion of precursor porphyrin, followed by intramolecular Scholl reaction. view more 

Credit: Ehime University

Prof. Okujima, in collaboration with Prof. Kobayashi at Shinshu University, reported the synthesis, molecular structure, optical properties and electronic structure of unusual phenanthrene-fused porphyrins.

Precursor porphyrins fused with aryl-substituted bicyclo[2.2.2]octadiene afforded the corresponding arylbenzoporphyrins (arylBPs) by retro Diels–Alder reaction. Unusual phenanthroporphyrins were obtained via the intramolecular Scholl reaction of arylBPs. We analyzed the optical and electronic structures using magnetic circular dichroism spectroscopy and time-dependent density functional theory calculations.

Our findings were published on April 25, 2023 in Organic Letters.


Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.