A Highly Stable Organic Luminescent Diradical

Author:

Abdurahman Alim1ORCID,Wang Jingmin2,Zhao Yihan3,Li Ping4,Shen Li5ORCID,Peng Qiming2ORCID

Affiliation:

1. State Key Laboratory of Integrated Optoelectronics College of Electronic Science and Engineering Jilin University Qianjin Avenue 2699 Changchun 130012 P. R. China

2. Key Laboratory of Flexible Electronics (KLOFE) Institute of Advanced Materials (IAM) & School of Flexible Electronics (Future Technologies) Nanjing Tech University (NanjingTech) 30 South Puzhu Road Nanjing 211816 China

3. State Key Laboratory of Supramolecular Structure and Materials College of Chemistry Jilin University Qianjin Avenue 2699 Changchun 130012 P. R. China

4. Key Laboratory for Organic Electronics and Information Displays & Institute of Advanced Materials (IAM) National Synergistic Innovation Center for Advanced Materials (SICAM) Nanjing University of Posts & Telecommunications 9 Wenyuan Road Nanjing 210023 P. R. China

5. College of Chemical Engineering and Environmental Chemistry Weifang University Weifang 261061 China

Abstract

AbstractIt is very challenging to obtain stable room‐temperature luminescent open‐shell singlet diradicals. Herein we report the first stable Müller's hydrocarbon TTM‐PhTTM with luminescent properties. Variable‐temperature electron paramagnetic resonance spectroscopy measurements and theoretical calculations show that TTM‐PhTTM has an open‐shell singlet ground state with a diradical character of 90 %. Because of a small singlet‐triplet energy gap, the open‐shell singlet ground state can be thermally excited to a triplet state. TTM‐PhTTM shows room‐temperature deep‐red emission in various solutions. Unusually high stability of TTM‐PhTTM was also observed owing to effective steric hindrance and spin delocalization. Our results are beneficial to the rational design and discovery of more stable luminescent diradical materials.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

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