Synthesis and luminescent properties of Eu3+ organic complex PVA encapsulation film
Source abstract
Abstract
A complex with Eu[Formula: see text] as the luminescent center, 2-thiophenecarbonyl trifluoroacetone (TTA) as the first ligand and o-phenanthroline (Phen) as the co-ligand was designed and synthesized. The complex was then dispersed into polyvinyl alcohol (PVA) to form the Eu[Formula: see text]Tb[Formula: see text](TTA)3phen/PVA composite. The structure and reaction processes of the composites were analyzed by FE-SEM and XRD, and the optical properties of Eu[Formula: see text]Tb[Formula: see text](TTA)3phen complexes with different contents were analyzed by fluorescence spectroscopy.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Lanthanide and Transition Metal Complexes · Magnetism in coordination complexes · Luminescence Properties of Advanced Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry and Materials Science, Shanghai Normal University, Shanghai 200234, P. R. China
References (35)
Show source-provided references
1. Jiu H. · J. Non-Crystalline Solids. · 2006 · 3 · 352
2. 10.1021/acsenergylett.6b0005910.1021/acsenergylett.6b00059 ↗
3. 10.1021/ic501335e10.1021/ic501335e ↗
4. Al-Farsi Z. S. · Polyhedron · 2016
5. 10.1002/chem.20140625410.1002/chem.201406254 ↗
6. 10.1016/j.optmat.2012.02.04710.1016/j.optmat.2012.02.047 ↗
7. 10.1016/j.optmat.2015.05.03810.1016/j.optmat.2015.05.038 ↗
8. 10.1016/j.ccr.2011.12.01310.1016/j.ccr.2011.12.013 ↗
9. 10.1021/acs.inorgchem.0c0040510.1021/acs.inorgchem.0c00405 ↗
10. 10.1021/acsomega.9b0022310.1021/acsomega.9b00223 ↗
11. 10.1016/j.jallcom.2015.04.06610.1016/j.jallcom.2015.04.066 ↗
12. 10.1039/c3dt53407c10.1039/c3dt53407c ↗
13. 10.1016/0022-2313(91)90170-Z10.1016/0022-2313(91)90170-Z ↗
14. 10.1063/1.172370910.1063/1.1723709 ↗
15. 10.1063/1.175382110.1063/1.1753821 ↗
16. 10.1021/jacs.9b1169710.1021/jacs.9b11697 ↗
17. 10.1021/cr010287y10.1021/cr010287y ↗
18. 10.1016/0010-8545(90)80060-710.1016/0010-8545(90)80060-7 ↗
19. 10.1016/S0010-8545(98)00125-810.1016/S0010-8545(98)00125-8 ↗
20. 10.1016/S0254-0584(97)80274-X10.1016/S0254-0584(97)80274-X ↗
21. 10.1016/j.jlumin.2006.03.01210.1016/j.jlumin.2006.03.012 ↗
22. Kuriki K. · Chem. Rev. · 2002 · 10 · 22347
23. Prodius D. · Chem. Rev. · 2018 · 363 · 16
24. 10.1016/S0010-8545(99)00054-510.1016/S0010-8545(99)00054-5 ↗
25. 10.1016/j.jphotochemrev.2004.10.00310.1016/j.jphotochemrev.2004.10.003 ↗
26. 10.1016/j.ccr.2009.12.03610.1016/j.ccr.2009.12.036 ↗
27. 10.1021/cm900607410.1021/cm9006074 ↗
28. 10.1039/b914978c10.1039/b914978c ↗
29. 10.1039/c0nj00955e10.1039/c0nj00955e ↗
30. 10.1016/S0025-5408(98)00133-010.1016/S0025-5408(98)00133-0 ↗
31. 10.1007/s00396-015-3614-810.1007/s00396-015-3614-8 ↗
32. 10.1016/j.optmat.2015.10.02710.1016/j.optmat.2015.10.027 ↗
33. 10.1016/j.optmat.2015.07.04410.1016/j.optmat.2015.07.044 ↗
34. 10.1080/09500340.2019.158280810.1080/09500340.2019.1582808 ↗
35. Dong J. · Mater. Res. Exp. · 2017 · 4 · 2053