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

15 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

Access to Document

10.1039/c2cc30625e

Cite this

@article{4973a49aed634a96adc1d76301b64a11,

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

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",

year = "2012",

month = mar,

day = "21",

doi = "10.1039/c2cc30625e",

language = "English",

volume = "48",

pages = "3851--3853",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "32",

}

TY - JOUR

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.

UR - http://www.scopus.com/inward/record.url?scp=84859032776&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84859032776&partnerID=8YFLogxK

U2 - 10.1039/c2cc30625e

DO - 10.1039/c2cc30625e

M3 - Article

C2 - 22410631

AN - SCOPUS:84859032776

VL - 48

SP - 3851

EP - 3853

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 32

ER -

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

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this