Direct Photopatterning of BODIPY‐Based Small Molecules via Thiol‐ene Click Chemistry
Source abstract
Abstract
Abstract We demonstrate a BODIPY‐based small molecule photopatterned surface by thiol‐ene click chemistry at room temperature utilizing only 366 nm UV light. The resulting cross‐linked polymer exhibits porous surfaces according to AFM and TEM results. A dramatic blue shift occurred in absorption spectra and the photoluminescence was also intensified as a result of crosslinking. Optical and electrochemical results are compatible with the DFT calculations. The obtained results prove that the photopatterned BODIPY‐based material can be easily and inexpensively applied in multilayer optoelectronic devices.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research · Nanoplatforms for cancer theranostics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry Marmara University 34722 Istanbul Turkey
Department of Chemical Engineering Çanakkale Onsekiz Mart University 17100 Çanakkale Turkey
Department of Chemistry Gebze Technical University 41400 Kocaeli Turkey
Department of Chemistry Bursa Technical University 16310 Bursa Turkey
Funding
Marmara Üniversitesi
References (41)
Show source-provided references
1.
2. 10.1002/anie.20090392410.1002/anie.200903924 ↗
3. 10.1002/ange.20090392410.1002/ange.200903924 ↗
4. 10.1039/b110088m10.1039/b110088m ↗
5. 10.1039/B9PY00216B10.1039/B9PY00216B ↗
6.
7. 10.1002/macp.20170007310.1002/macp.201700073 ↗
8. 10.1038/pj.2014.7910.1038/pj.2014.79 ↗
9. 10.1002/macp.20090044210.1002/macp.200900442 ↗
10.
11. 10.1039/D1TC00283J10.1039/D1TC00283J ↗
12. 10.1016/j.dyepig.2021.10950710.1016/j.dyepig.2021.109507 ↗
13. 10.1021/acsami.6b0866710.1021/acsami.6b08667 ↗
14.
15. 10.1021/cr050139y10.1021/cr050139y ↗
16. 10.1021/acs.chemrev.8b0006310.1021/acs.chemrev.8b00063 ↗
17. 10.1021/acsapm.9b0005210.1021/acsapm.9b00052 ↗
18. 10.1021/acs.macromol.6b0136710.1021/acs.macromol.6b01367 ↗
19. 10.1021/acs.macromol.6b0128110.1021/acs.macromol.6b01281 ↗
20. 10.1039/C7MH00488E10.1039/C7MH00488E ↗
21.
22. 10.1039/c3tc32098g10.1039/c3tc32098g ↗
23. 10.1021/ma501422610.1021/ma5014226 ↗
24. 10.1002/smll.20070125110.1002/smll.200701251 ↗
25. 10.1021/ja208857910.1021/ja2088579 ↗
26. 10.1002/adfm.20120300510.1002/adfm.201203005 ↗
27. 10.1021/cr078381n10.1021/cr078381n ↗
28. 10.1002/anie.20070207010.1002/anie.200702070 ↗
29. 10.1002/ange.20070207010.1002/ange.200702070 ↗
30. 10.3390/molecules2601015310.3390/molecules26010153 ↗
31.
32. 10.1016/j.solener.2019.04.09310.1016/j.solener.2019.04.093 ↗
33. 10.1039/C5TA04229A10.1039/C5TA04229A ↗
34. 10.1016/j.progpolymsci.2017.02.00310.1016/j.progpolymsci.2017.02.003 ↗
35. 10.1016/j.electacta.2013.07.17910.1016/j.electacta.2013.07.179 ↗
36. 10.1039/C4CC02567A10.1039/C4CC02567A ↗
37. 10.1039/C7NR06848D10.1039/C7NR06848D ↗
38. 10.1016/j.dyepig.2018.01.02310.1016/j.dyepig.2018.01.023 ↗
39.
40. 10.1021/ja408093p10.1021/ja408093p ↗
41. 10.1039/c3ra41298a10.1039/c3ra41298a ↗