journal article·2025Open access

Electron rich N-heterotriangulenes as host materials for OLEDs

Stefan Warrington, Joseph Cameron, Claire Wilson, Dmytro Volyniuk, Dylan Wilkinson, Juozas Vidas Grazulevicius, Peter J. Skabara, Graeme Cooke

Journal of Materials Chemistry C· Volume 13· Issue 31

Abstract

In this work, we present a series of N-heterotriangulenes featuring electron-rich, electronically discrete bridging moieties forming distinct 3D structures. We investigate their physical properties and performance in OLED devices.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short

Research context

OpenAlex topics: Ferrocene Chemistry and Applications · Magnetism in coordination complexes · Synthesis and properties of polymers

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

Affiliations

School of Chemistry, University of Glasgow, University Place, Glasgow, G12 8QQ, UK

Department of Polymer Chemistry and Technology, Kaunas University of Technology, Barsausko 59, LT-51423, Kaunas, Lithuania

Funding

Lietuvos Mokslo Taryba · Engineering and Physical Sciences Research Council

References (33)

Show source-provided references
1. Blanchard · Polym. Int. · 2019 · 68 · 58910.1002/pi.5695 ↗
2. Agarwala · J. Mater. Chem. A · 2017 · 5 · 134810.1039/C6TA08449D ↗
3. Farokhi · J. Mater. Chem. A · 2023 · 11 · 2513610.1039/D3TA03585A ↗
4. Farokhi · Chem. Soc. Rev. · 2022 · 51 · 597410.1039/D1CS01157J ↗
5. Munshi · Phys. Chem. Chem. Phys. · 2017 · 19 · 1988110.1039/C7CP02638B ↗
6. Sobolev · Acta Crystallogr. C · 1985 · 41 · 96710.1107/S0108270185006217 ↗
7. Hirai · Chem. Rev. · 2019 · 119 · 829110.1021/acs.chemrev.8b00637 ↗
8. Hammer · Chem. Rec. · 2015 · 15 · 111910.1002/tcr.201500202 ↗
9. Hellwinkel · Chem. Ber. · 1971 · 104 · 100110.1002/cber.19711040406 ↗
10. Hellwinkel · Chem. Ber. · 1974 · 107 · 61610.1002/cber.19741070231 ↗
11. Karjule · J. Mater. Chem. A · 2016 · 4 · 1891010.1039/C6TA08651A ↗
12. Choi · J. Mater. Chem. A · 2014 · 2 · 1913610.1039/C4TA04179H ↗
13. Fang · J. Mater. Chem. · 2012 · 22 · 1539710.1039/c2jm32840b ↗
14. Chen · Adv. Mater. · 2017 · 29 · 170276710.1002/adma.201702767 ↗
15. Kervella · J. Mater. Chem. C · 2023 · 11 · 816110.1039/D2TC05424H ↗
16. Petkus · Chem. Heterocycl. Compd. · 2020 · 56 · 51210.1007/s10593-020-02691-8 ↗
17. Jiang · Org. Lett. · 2009 · 11 · 150310.1021/ol9001152 ↗
18. Jiang · Chem. Mater. · 2011 · 23 · 77110.1021/cm1018585 ↗
19. Liu · Chem. – Eur. J. · 2012 · 18 · 692810.1002/chem.201200062 ↗
20. Zhang · Chem. Sci. · 2017 · 8 · 780710.1039/C7SC03543H ↗
21. Wu · Synth. Met. · 2015 · 205 · 7010.1016/j.synthmet.2015.03.033 ↗
22. Zhao · Dyes Pigm. · 2017 · 140 · 27810.1016/j.dyepig.2017.01.051 ↗
23. Reddy · Chem. – Eur. J. · 2018 · 24 · 642610.1002/chem.201706104 ↗
24. Schaub · Chem. – Eur. J. · 2020 · 26 · 326410.1002/chem.202000355 ↗
25. Krug · Angew. Chem., Int. Ed. · 2020 · 59 · 1623310.1002/anie.202003504 ↗
26. Ward · Chem. Mater. · 2019 · 31 · 668410.1021/acs.chemmater.9b01184 ↗
27. Gauthier Jean · Stuttg · 1987 · 4 · 383
28. Pan · Comput. Mater. Sci. · 2006 · 38 · 10510.1016/j.commatsci.2006.01.011 ↗
29. Cias · J. Phys. Chem. A · 2011 · 115 · 1451910.1021/jp207585j ↗
30. Poplavskyy · J. Appl. Phys. · 2003 · 93 · 34110.1063/1.1525866 ↗
31. Suzuki · J. Mater. Chem. C · 2015 · 3 · 170010.1039/C4TC02211D ↗
32. Komatsu · Synth. Met. · 2015 · 202 · 16510.1016/j.synthmet.2015.02.009 ↗
33. Etherington · J. Phys. Chem. C · 2019 · 123 · 1110910.1021/acs.jpcc.9b01458 ↗