Sustainable access to perylenedicarboxylic monoimides and diesters enables processable 3,3′-biperylene derivatives with large Stokes shifts
Source abstract
Abstract
The access to 3,4-perylenedicarboxylic monoanhydride allows the preparation of 3,3′-biperylene derivatives having large Stokes shifts (>250 meV) and quantum yields (>80%), improved solubilities and reduced aggregation propensity.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short
Research context
OpenAlex topics: Cyclization and Aryne Chemistry · Organic Electronics and Photovoltaics · Synthetic Organic Chemistry Methods
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science, University of Milano-Bicocca, via R. Cozzi 55, 20126, Milan, Italy
Funding
European Regional Development Fund
References (30)
Show source-provided references
1. Sun · Chem. Soc. Rev. · 2016 · 45 · 151310.1039/C5CS00754B ↗
2. Krupka · Int. J. Mol. Sci. · 2023 · 24 · 630810.3390/ijms24076308 ↗
3. Mohapatra · ACS Appl. Mater. Interfaces · 2023 · 15 · 2522410.1021/acsami.3c02003 ↗
4. Alonso-Navarro · Org. Lett. · 2025 · 27 · 961310.1021/acs.orglett.5c02655 ↗
5. Zhou · Sci. Total Environ. · 2021 · 780 · 14648310.1016/j.scitotenv.2021.146483 ↗
6. Roy · Org. Mater. · 2021 · 3 · 41710.1055/a-1551-6930 ↗
7. Roy · J. Mater. Chem. B · 2022 · 10 · 535210.1039/D2TB00349J ↗
8. Gandini · Nat. Nanotechnol. · 2020 · 15 · 46210.1038/s41565-020-0683-8 ↗
9. Langhals · J. Org. Chem. · 2012 · 77 · 958510.1021/jo301417p ↗
10. Langhals · J. Prakt. Chem. · 1999 · 341 · 30910.1002/(SICI)1521-3897(199904)341:3<309::AID-PRAC309>3.0.CO;2-F ↗
11. Langhals · J. Phys. Chem. A · 2020 · 124 · 155410.1021/acs.jpca.9b11225 ↗
12. Zucchi · ACS Sustainable Chem. Eng. · 2024 · 12 · 853310.1021/acssuschemeng.4c02041 ↗
13. Langhals · Liebigs Ann./Recl. · 1997 · 1997 · 46710.1002/jlac.199719970305 ↗
14. Feiler · Liebigs Ann. · 1995 · 1995 · 122910.1002/jlac.1995199507164 ↗
15. Chen · Ind. Eng. Chem. Res. · 2015 · 54 · 1269910.1021/acs.iecr.5b04203 ↗
16. Đorđević · Angew. Chem., Int. Ed. · 2023 · 62 · e20221499710.1002/anie.202214997 ↗
17. Langhals · J. Org. Chem. · 2012 · 77 · 958510.1021/jo301417p ↗
18. Langhals · J. Org. Chem. · 2019 · 84 · 542510.1021/acs.joc.9b00409 ↗
19. Arthur Sheldon · Green Chem. · 2023 · 25 · 170410.1039/D2GC04747K ↗
20. Roy · Org. Mater. · 2021 · 3 · 41710.1055/a-1551-6930 ↗
21. Ghiglietti · Energy Adv. · 2022 · 1 · 39810.1039/D2YA00135G ↗
22. Cremer · Eur. J. Org. Chem. · 2005 · 371510.1002/ejoc.200500147 ↗
23. Turrisi · J. Mater. Chem. A · 2015 · 3 · 804510.1039/C5TA01134E ↗
24. Aydin · New J. Chem. · 2014 · 39 · 54810.1039/C4NJ01565G ↗
25. Lindquist · J. Am. Chem. Soc. · 2014 · 136 · 1491210.1021/ja507653p ↗
26. Yang · J. Mater. Chem. · 2001 · 11 · 242010.1039/b102741g ↗
27. Sanguineti · Chem. Commun. · 2013 · 49 · 161810.1039/c2cc38708e ↗
28. Meinardi · Nat. Rev. Mater. · 2017 · 2 · 1707210.1038/natrevmats.2017.72 ↗
29. Griffini · Front. Mater. · 2019 · 6 · 110.3389/fmats.2019.00029 ↗
30. Sekita · Chem. – Eur. J. · 2015 · 21 · 1902810.1002/chem.201503237 ↗