Fluorescence enhancement of Tetraazaporphyrins by the use of bulky substituent effects

Takuya Yoshida; Taniyuki Furuyama; Mitsuo Asai; Nagao Kobayashi

doi:10.1246/cl.150304

Fluorescence enhancement of Tetraazaporphyrins by the use of bulky substituent effects

Takuya Yoshida, Taniyuki Furuyama, Mitsuo Asai, Nagao Kobayashi

SCI - Chemistry

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

3 Citations (Scopus)

Abstract

Tetraazaporphyrins substituted with bulky aryl groups have been synthesized and their fluorescence properties were investigated. The structural effects of the bulky groups were estimated by X-ray crystallographic analysis. The fluorescence quantum yields of these compounds were successfully enhanced due to the effect of the bulky substituent groups.

Original language	English
Pages (from-to)	1056-1058
Number of pages	3
Journal	Chemistry Letters
Volume	44
Issue number	8
DOIs	https://doi.org/10.1246/cl.150304
Publication status	Published - 2015

ASJC Scopus subject areas

Chemistry(all)

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10.1246/cl.150304

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title = "Fluorescence enhancement of Tetraazaporphyrins by the use of bulky substituent effects",

abstract = "Tetraazaporphyrins substituted with bulky aryl groups have been synthesized and their fluorescence properties were investigated. The structural effects of the bulky groups were estimated by X-ray crystallographic analysis. The fluorescence quantum yields of these compounds were successfully enhanced due to the effect of the bulky substituent groups.",

author = "Takuya Yoshida and Taniyuki Furuyama and Mitsuo Asai and Nagao Kobayashi",

note = "Publisher Copyright: {\textcopyright} 2015 The Chemical Society of Japan.",

year = "2015",

doi = "10.1246/cl.150304",

language = "English",

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pages = "1056--1058",

journal = "Chemistry Letters",

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T1 - Fluorescence enhancement of Tetraazaporphyrins by the use of bulky substituent effects

AU - Yoshida, Takuya

AU - Furuyama, Taniyuki

AU - Asai, Mitsuo

AU - Kobayashi, Nagao

PY - 2015

Y1 - 2015

N2 - Tetraazaporphyrins substituted with bulky aryl groups have been synthesized and their fluorescence properties were investigated. The structural effects of the bulky groups were estimated by X-ray crystallographic analysis. The fluorescence quantum yields of these compounds were successfully enhanced due to the effect of the bulky substituent groups.

AB - Tetraazaporphyrins substituted with bulky aryl groups have been synthesized and their fluorescence properties were investigated. The structural effects of the bulky groups were estimated by X-ray crystallographic analysis. The fluorescence quantum yields of these compounds were successfully enhanced due to the effect of the bulky substituent groups.

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U2 - 10.1246/cl.150304

DO - 10.1246/cl.150304

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VL - 44

SP - 1056

EP - 1058

JO - Chemistry Letters

JF - Chemistry Letters

SN - 0366-7022

IS - 8

ER -

Fluorescence enhancement of Tetraazaporphyrins by the use of bulky substituent effects

Abstract

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