Issue 68, 2019

Synthesis and electronic properties of π-expanded carbazole-based porphyrins

Abstract

Peripheral π-expansion of carbazole-based porphyrins was achieved for the first time by the Pt-catalyzed cyclization and the incorporation of a benzocarbazole unit. These two types of fused porphyrins showed red-shifted and broad NIR absorption due to the expanded π-conjugation as confirmed by NIR absorption spectroscopy and DFT calculations.

Graphical abstract: Synthesis and electronic properties of π-expanded carbazole-based porphyrins

Supplementary files

Article information

Article type
Communication
Submitted
03 Jul 2019
Accepted
30 Jul 2019
First published
31 Jul 2019

Chem. Commun., 2019,55, 10162-10165

Synthesis and electronic properties of π-expanded carbazole-based porphyrins

C. Maeda, Y. Tanaka, T. Shirakawa and T. Ema, Chem. Commun., 2019, 55, 10162 DOI: 10.1039/C9CC05079E

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