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Synthesis of peripherally annulated phenanthroporphyrins

06.26.23 | Ehime University

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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 .

Organic Letters

10.1021/acs.orglett.3c00876

25-Apr-2023

Keywords

Article Information

Contact Information

Takuya Imaoka
Ehime University
koho@stu.ehime-u.ac.jp

Source

How to Cite This Article

APA:
Ehime University. (2023, June 26). Synthesis of peripherally annulated phenanthroporphyrins. Brightsurf News. https://www.brightsurf.com/news/8X5KX7O1/synthesis-of-peripherally-annulated-phenanthroporphyrins.html
MLA:
"Synthesis of peripherally annulated phenanthroporphyrins." Brightsurf News, Jun. 26 2023, https://www.brightsurf.com/news/8X5KX7O1/synthesis-of-peripherally-annulated-phenanthroporphyrins.html.