An excimer to exciplex transition through realization of donor–acceptor interactions in luminescent solvent-free liquids
Source abstract
Abstract
Luminescent solvent-free organic liquids are known for their enhanced quantum yield, color tunability, and availability of a matrix for other dopants to generate hybrid luminescent materials with improved features for newer applications. Herein, we report a donor-acceptor based luminescent "exciplex liquid" by utilizing the slightly different electron affinity of the acceptor molecules. A red-shifted broad exciplex emission exhibited by the donor-acceptor pair even at a lower concentration of the acceptor (0.001 equiv.) indicates high efficiency in the solvent-free state. A detailed NMR study revealed weak intermolecular interactions between the donor and acceptor in the solvent-free matrix that stabilizes the exciplex liquid. The failure of structurally similar solid counterparts to form an exciplex confirms the advantage of the available supportive liquid matrix. Besides, the luminescent exciplex liquid is found efficient in sensing application, which is unachievable by either the individual liquids or their solid counterparts. Here, a transition of a donor-acceptor pair from a solid to solvent-free liquid results in a new hybrid liquid that can be an alternative for solid sensor materials.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Molecular Sensors and Ion Detection · Supramolecular Chemistry and Complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Organic Chemistry Division
National Chemical Laboratory (CSIR-NCL)
Pune-411008
India
Academy of Scientific and Innovative Research (AcSIR)
Ghaziabad-201 002
Physical and Materials Chemistry Division
Central NMR Facility
Funding
University Grants Commission · Defence Research and Development Organisation
References (35)
Show source-provided references
1. Sandanayaka · Appl. Phys. Lett. · 2016 · 108 · 22330110.1063/1.4952970 ↗
2. Kobayashi · Sci. Rep. · 2015 · 5 · 1482210.1038/srep14822 ↗
3. Tsuwaki · Sens. Actuators, A · 2014 · 216 · 23110.1016/j.sna.2014.05.032 ↗
4. Hirata · Adv. Mater. · 2011 · 23 · 88910.1002/adma.201003505 ↗
5. Lu · Adv. Opt. Mater. · 2019 · 7 · 190017610.1002/adom.201900176 ↗
6. Sato · Chem. – Asian J. · 2018 · 13 · 261910.1002/asia.201800631 ↗
7. Babu · Phys. Chem. Chem. Phys. · 2015 · 17 · 395010.1039/C4CP05481D ↗
8. Snaith · Nano Lett. · 2006 · 6 · 200010.1021/nl061173a ↗
9. Duan · J. Am. Chem. Soc. · 2013 · 135 · 1905610.1021/ja411316s ↗
10. Jie · Angew. Chem., Int. Ed. · 2020 · 59 · 226810.1002/anie.201912068 ↗
11. Giri · Nature · 2015 · 527 · 21610.1038/nature16072 ↗
12. Goudappagouda · Angew. Chem., Int. Ed. · 2019 · 58 · 228410.1002/anie.201811834 ↗
13. Lu · Acc. Chem. Res. · 2019 · 52 · 183410.1021/acs.accounts.9b00217 ↗
14. Lu · J. Mater. Chem. C · 2019 · 7 · 257710.1039/C8TC06254D ↗
15. Mukhopadhyay · Angew. Chem., Int. Ed. · 2006 · 45 · 159210.1002/anie.200503158 ↗
16. Babu · Nat. Commun. · 2013 · 4 · 196910.1038/ncomms2969 ↗
17. Babu · Angew. Chem., Int. Ed. · 2012 · 51 · 339110.1002/anie.201108853 ↗
18. Ghosh · Nat. Commun. · 2019 · 10 · 421010.1038/s41467-019-12249-8 ↗
19. Allain · ACS Appl. Mater. Interfaces · 2016 · 8 · 1984310.1021/acsami.6b04677 ↗
20. Li · Langmuir · 2013 · 29 · 539410.1021/la400202r ↗
21. Wakchaure · Chem. Commun. · 2019 · 55 · 937110.1039/C9CC03671G ↗
22. Hollamby · Chem. Commun. · 2016 · 52 · 734410.1039/C6CC01517D ↗
23. Adachi · Chem. Lett. · 2014 · 43 · 177010.1246/cl.140587 ↗
24. Sun · Chem. Soc. Rev. · 2015 · 44 · 801910.1039/C5CS00496A ↗
25. McQuade · Chem. Rev. · 2010 · 100 · 253710.1021/cr9801014 ↗
26. Sanchez · Chem. Mater. · 2007 · 19 · 645910.1021/cm702299g ↗
27. Toal · Chem. Commun. · 2005 · 546510.1039/b509404f ↗
28. Rose · Nature · 2005 · 434 · 87610.1038/nature03438 ↗
29. Sohn · Angew. Chem., Int. Ed. · 2001 · 40 · 210410.1002/1521-3773(20010601)40:11<2104::AID-ANIE2104>3.0.CO;2-# ↗
30. Kolla · Angew. Chem., Int. Ed. Engl. · 1997 · 36 · 80010.1002/anie.199708001 ↗
31. Wan · Angew. Chem., Int. Ed. · 2018 · 57 · 1551010.1002/anie.201809844 ↗
32. Beyazkilic · ACS Appl. Mater. Interfaces · 2014 · 6 · 499710.1021/am406035v ↗
33. Kartha · J. Am. Chem. Soc. · 2012 · 134 · 483410.1021/ja210728c ↗
34. Liu · Langmuir · 2001 · 17 · 745210.1021/la010696p ↗
35. Goudappagouda · J. Mater. Chem. A · 2020 · 8 · 1076710.1039/D0TA02091E ↗