Photostability of luminescent tris(2,4,6-trichlorophenyl)methyl radical enhanced by terminal modification of carbazole donor-Reference-Cited by-同舟云学术

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

Published:2022 Issue:97 Volume:58 Page:13443-13446
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Matsuda Kenshiro¹,Xiaotian Rui¹,Nakamura Kazuhiro¹,Furukori Minori²³,Hosokai Takuya²³^ORCID,Anraku Kosuke¹,Nakao Kohei⁴,Albrecht Ken⁴⁵^ORCID

Affiliation:

1. Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasuga-Koen, Kasuga-shi, Fukuoka 816-8580, Japan

2. National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba Central 5, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565, Japan

3. Department of Pure and Applied Chemistry, Faculty of Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan

4. Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-Koen, Kasuga-shi, Fukuoka 816-8580, Japan

5. JST-PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan

Abstract

Phenyl-ring substitution to the 3,6-position of carbazole donor can enhance the photostability of organic luminescenet radical (TTM) 1 orders of magnitude.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Precursory Research for Embryonic Science and Technology

Japan Society for the Promotion of Science

Japan Science and Technology Agency

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CC/D2CC04481A

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5. A radical polymer with efficient deep-red luminescence in the condensed state

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