journal article·2018-01Open access

Synthesis and spectral properties of Methyl-Phenyl pyrazoloquinoxaline fluorescence emitters: Experiment and DFT/TDDFT calculations

P. Gąsiorski, M. Matusiewicz, E. Gondek, T. Uchacz, K. Wojtasik, A. Danel, Ya. Shchur, A.V. Kityk

Optical Materials· Volume 75

Abstract

Paper reports the synthesis and spectroscopic studies of two novel 1-Methyl-3-phenyl-1H-pyrazolo[3,4-b]quinoxaline (PQX) derivatives with 6-substituted methyl (MeMPPQX) or methoxy (MeOMPPQX) side groups. The optical absorption and fluorescence emission spectra are recorded in solvents of different polarity. Steady state and time-resolved spectroscopy provide photophysical characterization of MeMPPQX and MeOMPPQX dyes as materials for potential luminescence or electroluminescence applications. Measured optical absorption and fluorescence emission spectra are compared with quantum-chemical DFT/TDDFT calculations using long-range corrected xc-functionals, LRC-BLYP and CAM-B3LYP in combination with self-consistent reaction field model based on linear response (LR), state specific (SS) or corrected linear response (CLR) solvations. Performances of relevant theoretical models and approaches are compared. The reparameterized LRC-BLYP functional (ω = 0.231 Bohr−1) in combination with CLR solvation provides most accurate prediction of both excitation and emission energies. The MeMPPQX and MeOMPPQX dyes represent efficient fluorescence emitters in blue-green region of the visible spectra.
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Research context

OpenAlex topics: Synthesis and Biological Evaluation · Organic Light-Emitting Diodes Research · Photochemistry and Electron Transfer Studies

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References (51)

Show source-provided references
1. Tang · Appl. Phys. Lett. · 1997 · 51 · 91310.1063/1.98799 ↗
2. Wang · Displays · 2004 · 25 · 23710.1016/j.displa.2004.09.016 ↗
3. Nizioł · Macromol. Symp. · 2004 · 212 · 47310.1002/masy.200450860 ↗
4. Gondek · Polimery · 2004 · 49 · 16310.14314/polimery.2004.163 ↗
5. Ulla · Opt. Mater. · 2014 · 37 · 31110.1016/j.optmat.2014.06.016 ↗
6. Yang · Opt. Mater. · 2014 · 37 · 37610.1016/j.optmat.2014.06.029 ↗
7. Gondek · J. Mater. Sci. Mater. Electron. · 2011 · 22 · 10110.1007/s10854-010-0094-y ↗
8. Kim · Opt. Mater. · 2014 · 37 · 12010.1016/j.optmat.2014.05.010 ↗
9. Grykien · Opt. Mater. · 2014 · 37 · 19310.1016/j.optmat.2014.05.023 ↗
10. Kwon · Opt. Mater. · 2015 · 39 · 4010.1016/j.optmat.2014.10.060 ↗
11. Gondek · Mater. Lett. · 2006 · 60 · 330110.1016/j.matlet.2006.03.051 ↗
12. Guezguez · J. Phys. Chem. C · 2014 · 118 · 754510.1021/jp412204f ↗
13. Sofiani · Opt. Quant. Electron · 2016 · 4810.1007/s11082-016-0549-3 ↗
14. Migalska-Zalas · Opt. Mater. · 2012 · 34 · 163910.1016/j.optmat.2012.03.021 ↗
15. Gondek · Spectrochim. Acta A · 2004 · 60 · 310110.1016/j.saa.2004.02.022 ↗
16. Laurent · Int. J. Quantum Chem. · 2013 · 113 · 201910.1002/qua.24438 ↗
17. Całus · Opt. Commun. · 2006 · 268 · 6410.1016/j.optcom.2006.07.005 ↗
18. Mac · Pol. J. Chem. · 2007 · 81 · 557
19. Mac · J. Photochem. Photobiol. A Chem. · 2006 · 180 · 8810.1016/j.jphotochem.2005.09.027 ↗
20. Gąsiorski · Spectrochim. Acta A · 2017 · 186 · 8910.1016/j.saa.2017.05.060 ↗
21. Gąsiorski · J. Lumin. · 2017 · 192 · 28810.1016/j.jlumin.2017.06.022 ↗
22. Całus · Mater. Lett. · 2007 · 61 · 329210.1016/j.matlet.2006.11.055 ↗
23. Gondek · Spectrochim. Acta A · 2008 · 69 · 2210.1016/j.saa.2007.03.003 ↗
24. Jones · J. Phys. Chem. · 1985 · 89 · 29410.1021/j100248a024 ↗
25. Danel · Tetrahedron · 2017 · 73 · 507210.1016/j.tet.2017.06.061 ↗
26. Okuro · J. Org. Chem. · 2012 · 77 · 442010.1021/jo300173g ↗
27. Gallou-Dagommer · Org. Lett. · 2001 · 3 · 205310.1021/ol016018b ↗
28. Yanai · Chem. Phys. Lett. · 2004 · 393 · 5110.1016/j.cplett.2004.06.011 ↗
29. Lee · Phys. Rev. B · 1988 · 37 · 78510.1103/PhysRevB.37.785 ↗
30. Becke · Phys. Rev. A · 1988 · 38 · 309810.1103/PhysRevA.38.3098 ↗
31. Savin · 1996
32. Gill · Mol. Phys. · 1996 · 88 · 100510.1080/00268979609484488 ↗
33. Tawada · J. Chem. Phys. · 2004 · 120 · 842510.1063/1.1688752 ↗
34. Gąsiorski · J. Fluoresc. · 2012 · 22 · 8110.1007/s10895-011-0932-1 ↗
35. Gąsiorski · Mater. Chem. Phys. · 2012 · 132 · 33010.1016/j.matchemphys.2011.11.025 ↗
36. Wong · J. Chem. Phys. · 2008 · 129 · 21470310.1063/1.3025924 ↗
37. Balanay · Bull. Korean Chem. Soc. · 2011 · 32 · 70510.5012/bkcs.2011.32.2.705 ↗
38. Balanay · J. Phys. Chem. C · 2011 · 115 · 1942410.1021/jp205512v ↗
39. Kityk · J. Phys. Chem. A · 2012 · 116 · 304810.1021/jp300305j ↗
40. Kityk · Spectrochim. Acta A · 2014 · 128 · 37010.1016/j.saa.2014.02.109 ↗
41. Frisch · 2013
42. Caricato · J. Chem. Phys. · 2006 · 124 · 12452010.1063/1.2183309 ↗
43. Improta · J. Chem. Phys. · 2006 · 125 · 05410310.1063/1.2222364 ↗
44. Improta · J. Chem. Phys. · 2007 · 127 · 07450410.1063/1.2757168 ↗
45. SCRF (http://gaussian.com/scrf/).
46. C. Guido, S. Caprasecca, Corrected Linear Response: State-specific correction to solvent polarization response (https://molecolab.dcci.unipi.it/tools/white-papers/pisalr/).
47. Cammi · J. Chem. Phys. · 2005 · 122 · 10451310.1063/1.1867373 ↗
48. Corni · J. Chem. Phys. · 2005 · 123 · 13451210.1063/1.2039077 ↗
49. Caricato · Comput. Teor. Chem. · 2014 · 10401041 · 99
50. Kapturkiewicz · J. Phys. Chem. A · 1997 · 101 · 233210.1021/jp9634565 ↗
51. A.R. Allouche, Gabedit is a free Graphical User Interface for computational chemistry packages. It is available from: http://gabedit.sourceforge.net/.