Li‐Na Diao
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Li‐Na Diao has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Han-Yuan Gong
College of Chemistry, Beijing Normal University, No. 19, XinWai St, HaiDian District, Beijing, 100875, China
2 shared publications - Nai-Te Yao
College of Chemistry, Beijing Normal University, No. 19, XinWai St, HaiDian District, Beijing, 100875, China
2 shared publications - Xu-Lang Chen
College of Chemistry and Chemical Engineering, Hubei Key Laboratory of Pollutant Analysis and Reuse Technology, Hubei Normal University, Huangshi, 435002, P. R. China
2 shared publications - Yang Yang
College of Chemistry Beijing Normal University No. 19, XinJieKouWai St, HaiDian District Beijing 100875 P. R. China
2 shared publications - Yun-Jia Shen
College of Chemistry Beijing Normal University No. 19, XinJieKouWai St, HaiDian District Beijing 100875 P. R. China
2 shared publications
Latest Publications
- 3 March 2023
- Published by Wiley in Angewandte Chemie
- Vol. 135 (15)
A π‐Extended Pentadecabenzo[9]Helicene
A novel chiral nanographene (i.e. EP9H) with a pentadecabenzo[9]helicene core fragment has been synthesized and fully characterized. Single‐crystal X‐ray diffraction unambiguously confirms the helical structure. The fluorescence emission of EP9H is located in the near infrared region (λem=684 nm) with a medium quantum yield (0.10) for helicene derivatives. Cyclic voltammetry reveals its seven quasi‐reversible redox states from −2 to +5. Furthermore, enantiopure EP9H displays distinct CD signals in a broad spectral range from 300 to 700 nm. Notably, compared to the reported small organic molecules, EP9H displays an outstanding |glum| value of 4.50×10−2 and BCPL as 304 M−1 cm−1.
- 3 March 2023
- Published by Wiley in Angewandte Chemie
- Vol. 135 (15)
A π‐Extended Pentadecabenzo[9]Helicene
A novel chiral nanographene (i.e. EP9H) with a pentadecabenzo[9]helicene core fragment has been synthesized and fully characterized. Single‐crystal X‐ray diffraction unambiguously confirms the helical structure. The fluorescence emission of EP9H is located in the near infrared region (λem=684 nm) with a medium quantum yield (0.10) for helicene derivatives. Cyclic voltammetry reveals its seven quasi‐reversible redox states from −2 to +5. Furthermore, enantiopure EP9H displays distinct CD signals in a broad spectral range from 300 to 700 nm. Notably, compared to the reported small organic molecules, EP9H displays an outstanding |glum| value of 4.50×10−2 and BCPL as 304 M−1 cm−1.
- 3 March 2023
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 62 (15) , e202300840
A π‐Extended Pentadecabenzo[9]Helicene
A novel chiral nanographene (i.e. EP9H) with a pentadecabenzo[9]helicene core fragment has been synthesized and fully characterized. Single‐crystal X‐ray diffraction unambiguously confirms the helical structure. The fluorescence emission of EP9H is located in the near infrared region (λem=684 nm) with a medium quantum yield (0.10) for helicene derivatives. Cyclic voltammetry reveals its seven quasi‐reversible redox states from −2 to +5. Furthermore, enantiopure EP9H displays distinct CD signals in a broad spectral range from 300 to 700 nm. Notably, compared to the reported small organic molecules, EP9H displays an outstanding |glum| value of 4.50×10−2 and BCPL as 304 M−1 cm−1.
- 3 March 2023
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 62 (15) , e202300840
A π‐Extended Pentadecabenzo[9]Helicene
A novel chiral nanographene (i.e. EP9H) with a pentadecabenzo[9]helicene core fragment has been synthesized and fully characterized. Single‐crystal X‐ray diffraction unambiguously confirms the helical structure. The fluorescence emission of EP9H is located in the near infrared region (λem=684 nm) with a medium quantum yield (0.10) for helicene derivatives. Cyclic voltammetry reveals its seven quasi‐reversible redox states from −2 to +5. Furthermore, enantiopure EP9H displays distinct CD signals in a broad spectral range from 300 to 700 nm. Notably, compared to the reported small organic molecules, EP9H displays an outstanding |glum| value of 4.50×10−2 and BCPL as 304 M−1 cm−1.