Tuning optical properties of phenanthroline derivatives through varying excitation wavelength and pH values
Source abstract
Abstract
Two phenanthroline derivatives have been prepared to possess two cores and their tuneable emission behaviors have been investigated.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research · Photochemistry and Electron Transfer Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry
Chemical Engineering and Materials Science
Collaborative Innovation Center of Suzhou Nano Science and Technology
Soochow University
Suzhou 215123, China
School of Materials Science and Engineering
Nanyang Technological University
Singapore 639798, Singapore
References (31)
Show source-provided references
1. Li · J. Am. Chem. Soc. · 2013 · 135 · 1492410.1021/ja407508v ↗
2. Zhang · Chem. Commun. · 2013 · 49 · 980010.1039/c3cc46297h ↗
3. Olejniczak · ACS Macro Lett. · 2013 · 2 · 68310.1021/mz400256x ↗
4. Zhang · Adv. Mater. · 2008 · 20 · 209910.1002/adma.200702681 ↗
5. Sagara · Angew. Chem., Int. Ed. · 2011 · 50 · 912810.1002/anie.201100914 ↗
6. Davis · Nature · 2009 · 459 · 6810.1038/nature07970 ↗
7. Ooyama · J. Mater. Chem. · 2011 · 21 · 837210.1039/c0jm03601c ↗
8. Teng · Chem. Commun. · 2011 · 47 · 607810.1039/c1cc10873e ↗
9. Zhang · Inorg. Chem. · 2010 · 49 · 1074710.1021/ic902591s ↗
10. Gu · Chem.–Asian J. · 2013 · 8 · 216110.1002/asia.201300331 ↗
11. Hu · Acc. Chem. Res. · 2007 · 40 · 109710.1021/ar700046m ↗
12. Zhou · J. Mater. Chem. C · 2013 · 1 · 74410.1039/C2TC00111J ↗
13. Jin · Chem. Commun. · 2012 · 48 · 1042210.1039/c2cc35685f ↗
14. Demchenko · Luminescence · 2002 · 17 · 1910.1002/bio.671 ↗
15. Liu · Macromolecules · 2010 · 43 · 492110.1021/ma902432m ↗
16. Józefowicz · J. Fluoresc. · 2010 · 21 · 23910.1007/s10895-010-0711-4 ↗
17. Józefowicz · Chem. Phys. · 2007 · 338 · 5310.1016/j.chemphys.2007.07.035 ↗
18. Berezin · Chem.–Eur. J. · 2009 · 15 · 356010.1002/chem.200801784 ↗
19. Dong · J. Am. Chem. Soc. · 2007 · 129 · 1008410.1021/ja073622u ↗
20. Saleh · Spectrochim. Acta, Part A · 2008 · 71 · 81810.1016/j.saa.2008.02.004 ↗
21. Tang · Synth. Met. · 2009 · 159 · 7210.1016/j.synthmet.2008.07.025 ↗
22. Jansson · Chem. Phys. · 2006 · 330 · 16610.1016/j.chemphys.2006.08.010 ↗
23. Kim · Adv. Funct. Mater. · 2006 · 16 · 231710.1002/adfm.200500928 ↗
24. Gu · J. Mater. Chem. C · 2013 · 1 · 259910.1039/c3tc00738c ↗
25. Zhang · Photochem. Photobiol. Sci. · 2012 · 11 · 141410.1039/c2pp05404c ↗
26. Xu · J. Opt. Soc. Am. B · 1996 · 13 · 48110.1364/JOSAB.13.000481 ↗
27. Tao · Dyes Pigm. · 2010 · 84 · 15310.1016/j.dyepig.2009.07.007 ↗
28. Gibson · J. Am. Chem. Soc. · 2012 · 134 · 53910.1021/ja208917m ↗
29. Bryant · J. Chem. Phys. · 2013 · 78 · 1038
30. Das · Macromolecules · 2012 · 45 · 541010.1021/ma3006697 ↗
31. Garzon · J. Chem. Phys. · 2010 · 132 · 06490110.1063/1.3309585 ↗