journal article·2026

Regioselective synthesis of multifunctional dibenzo-heterocyclic dihydrophenazine derivatives: tunable excited-state structural relaxation and efficient red OLED host materials

Kai Kang, Chunyan Zhang, Yi Chen, Jinhai Huang, Xin Jin, Zhiyun Zhang

Journal of Materials Chemistry C· Volume 14· Issue 15
Publisher page

Abstract

A selective, efficient intramolecular amination strategy yields dihydrophenazine derivatives with distinct heteroatom doping. These structures modulate excited-state dynamics, making them promising for high-performance OLEDs.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Photochemistry and Electron Transfer Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Centre, Frontiers Science Center for Materiobiology and Dynamic Chemistry, East China University of Science & Technology, Shanghai 200237, China

Shanghai Taoe Chemical Technology Co., Ltd, Shanghai 200030, P. R. China

Funding

Project 211 · National Natural Science Foundation of China · Science and Technology Commission of Shanghai Municipality

References (51)

Show source-provided references
1. Takeda · Acc. Chem. Res. · 2024 · 57 · 221910.1021/acs.accounts.4c00353 ↗
2. Zhao · Angew. Chem., Int. Ed. · 2024 · 63 · e20240496810.1002/anie.202404968 ↗
3. Wheeler · J. Am. Chem. Soc. · 2025 · 147 · 1973810.1021/jacs.5c03169 ↗
4. Schramm · J. Am. Chem. Soc. · 2025 · 147 · 324310.1021/jacs.4c13291 ↗
5. Hohenstein · J. Phys. Chem. A · 2009 · 113 · 87810.1021/jp809062x ↗
6. Tsuzuki · J. Am. Chem. Soc. · 2007 · 129 · 865610.1021/ja071372b ↗
7. Yin · Chem. Sci. · 2026 · 17 · 259910.1039/D5SC06741C ↗
8. Farias · Chem. Sci. · 2021 · 12 · 1511610.1039/D1SC04936D ↗
9. Ma · JACS Au. · 2023 · 3 · 183510.1021/jacsau.3c00268 ↗
10. Ju · Angew. Chem., Int. Ed. · 2025 · 64 · e20241438310.1002/anie.202414383 ↗
11. Man · Adv. Funct. Mater. · 2025 · 35 · 241265210.1002/adfm.202412652 ↗
12. Liang · Angew. Chem., Int. Ed. · 2019 · 58 · 1722010.1002/anie.201909076 ↗
13. Gong · J. Am. Chem. Soc. · 2025 · 147 · 2104110.1021/jacs.5c05873 ↗
14. Ma · J. Am. Chem. Soc. · 2025 · 147 · 1080310.1021/jacs.5c02567 ↗
15. Li · Angew. Chem., Int. Ed. · 2019 · 58 · 727810.1002/anie.201814629 ↗
16. Liu · J. Am. Chem. Soc. · 2025 · 147 · 365010.1021/jacs.4c15651 ↗
17. Gorelsky · Coord. Chem. Rev. · 2013 · 257 · 15310.1016/j.ccr.2012.06.016 ↗
18. Evano · Angew. Chem., Int. Ed. · 2019 · 58 · 755810.1002/anie.201806631 ↗
19. Li · Mater. Chem. Front. · 2022 · 6 · 162310.1039/D2QM00203E ↗
20. Qin · J. Mater. Chem. C · 2023 · 11 · 1429910.1039/D3TC02824K ↗
21. Shen · ACS Appl. Mater. Interfaces · 2025 · 17 · 1431210.1021/acsami.4c21196 ↗
22. Wang · Mater. Today Chem. · 2025 · 47 · 10279610.1016/j.mtchem.2025.102796 ↗
23. Wang · Chem. Eng. J. · 2025 · 524 · 16919910.1016/j.cej.2025.169199 ↗
24. Jin · J. Am. Chem. Soc. · 2022 · 144 · 488310.1021/jacs.1c12610 ↗
25. Wang · Angew. Chem., Int. Ed. · 2021 · 60 · 1946610.1002/anie.202107915 ↗
26. Zhao · Angew. Chem., Int. Ed. · 2023 · 62 · e20221671310.1002/anie.202216713 ↗
27. Zhang · J. Am. Chem. Soc. · 2015 · 137 · 850910.1021/jacs.5b03491 ↗
28. Jin · Angew. Chem. Novit. · 2025 · e7001210.1002/anov.70012 ↗
29. Chen · J. Am. Chem. Soc. · 2017 · 139 · 163610.1021/jacs.6b11789 ↗
30. Zhang · Angew. Chem., Int. Ed. · 2018 · 57 · 988010.1002/anie.201806385 ↗
31. Sun · Angew. Chem., Int. Ed. · 2020 · 59 · 1861110.1002/anie.202005466 ↗
32. Zou · J. Am. Chem. Soc. · 2022 · 144 · 1004210.1021/jacs.2c03671 ↗
33. Sun · J. Phys. Chem. C · 2024 · 128 · 1512410.1021/acs.jpcc.4c04954 ↗
34. Jin · Angew. Chem., Int. Ed. · 2023 · 62 · e20230557210.1002/anie.202305572 ↗
35. Zhang · Coord. Chem. Rev. · 2022 · 472 · 21476810.1016/j.ccr.2022.214768 ↗
36. Zhang · Chem. Sci. · 2020 · 11 · 752510.1039/D0SC01591A ↗
37. Li · Chem. Commun. · 2020 · 56 · 226010.1039/C9CC09997B ↗
38. Ruiz-Castillo · Chem. Rev. · 2016 · 116 · 1256410.1021/acs.chemrev.6b00512 ↗
39. Cho · J. Am. Chem. Soc. · 2011 · 133 · 599610.1021/ja111652v ↗
40. Oláh · J. Phys. Chem. A · 2002 · 106 · 388510.1021/jp014039h ↗
41. Morgenstern · J. Phys. Chem. A · 2017 · 121 · 434110.1021/acs.jpca.7b00630 ↗
42. Li · J. Am. Chem. Soc. · 2023 · 145 · 758010.1021/jacs.3c00942 ↗
43. Lu · J. Comput. Chem. · 2012 · 33 · 58010.1002/jcc.22885 ↗
44. CCDC 2448858: Experimental Crystal Structure Determination , 2026 10.5517/ccdc.csd.cc2n67fk10.5517/ccdc.csd.cc2n67fk ↗
45. CCDC 2448863: Experimental Crystal Structure Determination , 2026 10.5517/ccdc.csd.cc2n67lq10.5517/ccdc.csd.cc2n67lq ↗
46. CCDC 2448864: Experimental Crystal Structure Determination , 2026 10.5517/ccdc.csd.cc2n67mr10.5517/ccdc.csd.cc2n67mr ↗
47. CCDC 2448865: Experimental Crystal Structure Determination , 2026 10.5517/ccdc.csd.cc2n67ns10.5517/ccdc.csd.cc2n67ns ↗
48. CCDC 2448866: Experimental Crystal Structure Determination , 2026 10.5517/ccdc.csd.cc2n67pt10.5517/ccdc.csd.cc2n67pt ↗
49. CCDC 2448869: Experimental Crystal Structure Determination , 2026 10.5517/ccdc.csd.cc2n67sx10.5517/ccdc.csd.cc2n67sx ↗
50. CCDC 2448870: Experimental Crystal Structure Determination , 2026 10.5517/ccdc.csd.cc2n67ty10.5517/ccdc.csd.cc2n67ty ↗
51. CCDC 2448873: Experimental Crystal Structure Determination , 2026 10.5517/ccdc.csd.cc2n67x110.5517/ccdc.csd.cc2n67x1 ↗