Synthesis of a twisted azananographene featuring a diquinoxaline-fused pyrene

π-Extension from a diquinoxaline-fused pyrene led to a twisted azananographene (azaNG) exhibiting red emission. Although the azaNG was highly contorted, the electronic nature of the diquinoxaline-fused pyrene was confirmed to be retained, and thus it exhibited three-electron accepting ability as well as a low-lying LUMO level.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc02120k
Citations
2
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
1.87

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article

Synthesis of a twisted azananographene featuring a diquinoxaline-fused pyrene

Ziqiang Xu, Aihui Zhang, Fenghua Bai, Chaolumen Chaolumen et al.
2 citations
Chemical Communications
Synthesis and Properties of Aromatic Compounds
1.87
article

Synthesis of a twisted azananographene featuring a diquinoxaline-fused pyrene

Ziqiang Xu, Aihui Zhang, Fenghua Bai, Chaolumen Chaolumen, Yoshifumi Hashikawa, Zhiyu Zhang
article en
2 citations

Abstract

π-Extension from a diquinoxaline-fused pyrene led to a twisted azananographene (azaNG) exhibiting red emission. Although the azaNG was highly contorted, the electronic nature of the diquinoxaline-fused pyrene was confirmed to be retained, and thus it exhibited three-electron accepting ability as well as a low-lying LUMO level.

Chemical CommunicationsVol. 61(61)
Kyoto University (JP), Inner Mongolia University (CN), Kyoto Bunkyo University (JP), Kyoto University Institute for Chemical Research
Education Department of Inner Mongolia Autonomous Region, National Natural Science Foundation of China, Kyoto University
Life below water
Openalex Percentile: Top 15%
Synthesis and Properties of Aromatic Compounds
1.87
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