Synthesis of 5,10,15-triazaporphyrins-effect of benzo-annulation on the electronic structures

Soji Shimizu; Yuki Ito; Kazuaki Oniwa; Shoma Hirokawa; Yoshiaki Miura; Osamu Matsushita; Nagao Kobayashi

doi:10.1039/c2cc30625e

Synthesis of 5,10,15-triazaporphyrins-effect of benzo-annulation on the electronic structures

Soji Shimizu, Yuki Ito, Kazuaki Oniwa, Shoma Hirokawa, Yoshiaki Miura, Osamu Matsushita, Nagao Kobayashi

SCI - Chemistry

Research output: Contribution to journal › Article › peer-review

14 Citations (Scopus)

Abstract

Novel triazaporphyrins were synthesized using 1,9-dibromodipyrromethene as a key starting material. These triazaporphyrins exhibit comparatively intense Soret and Q bands in the UV/vis region due to their hybrid properties between porphyrins and phthalocyanines.

Original language	English
Pages (from-to)	3851-3853
Number of pages	3
Journal	Chemical Communications
Volume	48
Issue number	32
DOIs	https://doi.org/10.1039/c2cc30625e
Publication status	Published - 2012 Mar 21

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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abstract = "Novel triazaporphyrins were synthesized using 1,9-dibromodipyrromethene as a key starting material. These triazaporphyrins exhibit comparatively intense Soret and Q bands in the UV/vis region due to their hybrid properties between porphyrins and phthalocyanines.",

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AU - Shimizu, Soji

AU - Ito, Yuki

AU - Oniwa, Kazuaki

AU - Hirokawa, Shoma

AU - Miura, Yoshiaki

AU - Matsushita, Osamu

AU - Kobayashi, Nagao

PY - 2012/3/21

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AB - Novel triazaporphyrins were synthesized using 1,9-dibromodipyrromethene as a key starting material. These triazaporphyrins exhibit comparatively intense Soret and Q bands in the UV/vis region due to their hybrid properties between porphyrins and phthalocyanines.

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