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

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 - Mar 21 2012
Externally published	Yes

All Science Journal Classification (ASJC) codes

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.",

author = "Soji Shimizu and Yuki Ito and Kazuaki Oniwa and Shoma Hirokawa and Yoshiaki Miura and Osamu Matsushita and Nagao Kobayashi",

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T1 - Synthesis of 5,10,15-triazaporphyrins-effect of benzo-annulation on the electronic structures

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

Y1 - 2012/3/21

N2 - 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.

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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DO - 10.1039/c2cc30625e

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SN - 1359-7345

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ER -

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

Abstract

All Science Journal Classification (ASJC) codes

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