Photostability of luminescent tris(2,4,6-trichlorophenyl)methyl radical enhanced by terminal modification of carbazole donor

Kenshiro Matsuda; Rui Xiaotian; Kazuhiro Nakamura; Minori Furukori; Takuya Hosokai; Kosuke Anraku; Kohei Nakao; Ken Albrecht

doi:10.1039/d2cc04481a

Photostability of luminescent tris(2,4,6-trichlorophenyl)methyl radical enhanced by terminal modification of carbazole donor

Kenshiro Matsuda, Rui Xiaotian, Kazuhiro Nakamura, Minori Furukori, Takuya Hosokai, Kosuke Anraku, Kohei Nakao, Ken Albrecht

融合材料部門

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

抄録

Stable organic luminescent radicals have attracted much attention, but their stability under light irradiation is not yet satisfactory. New luminescent radicals (TTMs) based on terminal benzene ring modified carbazole donors were synthesized and evaluated. Their photostability (half-life under continuous laser irradiation) has improved by 1 order of magnitude compared to simple carbazole donors. This is a new molecular design strategy to improve the photostability of luminescent radicals without reducing other photophysical properties.

本文言語	英語
ジャーナル	Chemical Communications
DOI	https://doi.org/10.1039/d2cc04481a
出版ステータス	印刷中 - 2022

!!!All Science Journal Classification (ASJC) codes

触媒
電子材料、光学材料、および磁性材料
セラミックおよび複合材料
化学 (全般)
表面、皮膜および薄膜
金属および合金
材料化学

文献へのアクセス

10.1039/d2cc04481a

他のファイルとリンク

フィンガープリント

「Photostability of luminescent tris(2,4,6-trichlorophenyl)methyl radical enhanced by terminal modification of carbazole donor」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル

@article{16e4945078814325aed545a62c8cb4c5,

title = "Photostability of luminescent tris(2,4,6-trichlorophenyl)methyl radical enhanced by terminal modification of carbazole donor",

abstract = "Stable organic luminescent radicals have attracted much attention, but their stability under light irradiation is not yet satisfactory. New luminescent radicals (TTMs) based on terminal benzene ring modified carbazole donors were synthesized and evaluated. Their photostability (half-life under continuous laser irradiation) has improved by 1 order of magnitude compared to simple carbazole donors. This is a new molecular design strategy to improve the photostability of luminescent radicals without reducing other photophysical properties.",

author = "Kenshiro Matsuda and Rui Xiaotian and Kazuhiro Nakamura and Minori Furukori and Takuya Hosokai and Kosuke Anraku and Kohei Nakao and Ken Albrecht",

note = "Publisher Copyright: {\textcopyright} 2022 The Royal Society of Chemistry.",

year = "2022",

doi = "10.1039/d2cc04481a",

language = "English",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

}

TY - JOUR

T1 - Photostability of luminescent tris(2,4,6-trichlorophenyl)methyl radical enhanced by terminal modification of carbazole donor

AU - Matsuda, Kenshiro

AU - Xiaotian, Rui

AU - Nakamura, Kazuhiro

AU - Furukori, Minori

AU - Hosokai, Takuya

AU - Anraku, Kosuke

AU - Nakao, Kohei

AU - Albrecht, Ken

PY - 2022

Y1 - 2022

N2 - Stable organic luminescent radicals have attracted much attention, but their stability under light irradiation is not yet satisfactory. New luminescent radicals (TTMs) based on terminal benzene ring modified carbazole donors were synthesized and evaluated. Their photostability (half-life under continuous laser irradiation) has improved by 1 order of magnitude compared to simple carbazole donors. This is a new molecular design strategy to improve the photostability of luminescent radicals without reducing other photophysical properties.

AB - Stable organic luminescent radicals have attracted much attention, but their stability under light irradiation is not yet satisfactory. New luminescent radicals (TTMs) based on terminal benzene ring modified carbazole donors were synthesized and evaluated. Their photostability (half-life under continuous laser irradiation) has improved by 1 order of magnitude compared to simple carbazole donors. This is a new molecular design strategy to improve the photostability of luminescent radicals without reducing other photophysical properties.

UR - http://www.scopus.com/inward/record.url?scp=85142338941&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85142338941&partnerID=8YFLogxK

U2 - 10.1039/d2cc04481a

DO - 10.1039/d2cc04481a

M3 - Article

C2 - 36373670

AN - SCOPUS:85142338941

SN - 1359-7345

JO - Chemical Communications

JF - Chemical Communications

ER -