journal article·2023-09-27

Novel BODIPY-Based Photobase Generators for Photoinduced Polymerization

Shupei Yu, Ojasvita Reddy, Alperen Abaci, Yongling Ai, Yanmei Li, Hao Chen, Murat Guvendiren, Kevin D. Belfield, Yuanwei Zhang

ACS Applied Materials & Interfaces· Volume 15· Issue 38
Publisher page

Abstract

Photobase generators (PBGs) are compounds that utilize light-sensitive chemical-protecting groups to offer spatiotemporal control of releasing organic bases upon targeted light irradiation. PBGs can be implemented as an external control to initiate anionic polymerizations such as thiol-ene Michael addition reactions. However, there are limitations for common PBGs, including a short absorption wavelength and weak base release that lead to poor efficiency in photopolymerization. Therefore, there is a great need for visible-light-triggered PBGs that are capable of releasing strong bases efficiently. Here, we report two novel BODIPY-based visible-light-sensitive PBGs for light-induced activation of the thiol-ene Michael "click" reaction and polymerization. These PBGs were designed by connecting the BODIPY-based light-sensitive protecting group with tetramethylguanidine (TMG), a strong base. Moreover, we exploited the heavy atom effect to increase the efficiency of releasing TMG and the polymerization rate. These BODIPY-based PBGs exhibit extraordinary activity toward thiol-ene Michael addition-based polymerization, and they can be used in surface coating and polymer network formation of different thiol and vinyl monomers.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Photopolymerization techniques and applications · Photochromic and Fluorescence Chemistry · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

. . Department of Chemistry and Environmental Science, College of Science and Liberal Arts, New Jersey Institute of Technology, 323 Martin Luther King Jr. Blvd., Newark, New Jersey 07102, United States

. . Otto H. York Department of Chemical and Materials Engineering, New Jersey Institute of Technology, 161 Warren Street, Newark, New Jersey 07102, United States

Funding

Division of Chemistry · National Institute on Alcohol Abuse and Alcoholism · New Jersey Health Foundation · BD · National Science Foundation · Division of Materials Research · New Jersey Institute of Technology

References (58)

Show source-provided references
1. 10.1002/1521-3773(20010601)40:11<2004::AID-ANIE2004>3.0.CO;2-510.1002/1521-3773(20010601)40:11<2004::AID-ANIE2004>3.0.CO;2-5 ↗
2. 10.1021/cm402180t10.1021/cm402180t ↗
3. 10.1021/mz500132j10.1021/mz500132j ↗
4. 10.1039/D0PY01593H10.1039/D0PY01593H ↗
5. 10.1021/acs.chemrev.0c0099710.1021/acs.chemrev.0c00997 ↗
6. 10.1016/j.eurpolymj.2020.10980410.1016/j.eurpolymj.2020.109804 ↗
7. 10.1016/j.eurpolymj.2021.11068610.1016/j.eurpolymj.2021.110686 ↗
8. 10.1016/j.jcis.2021.03.00610.1016/j.jcis.2021.03.006 ↗
9. 10.1039/C9PY01123D10.1039/C9PY01123D ↗
10. 10.1002/adma.20160529310.1002/adma.201605293 ↗
11. 10.1039/C9PY00953A10.1039/C9PY00953A ↗
12. 10.1002/adem.20220074910.1002/adem.202200749 ↗
13. 10.1021/acs.biomac.0c0130210.1021/acs.biomac.0c01302 ↗
14. 10.1002/pol.2019027910.1002/pol.20190279 ↗
15. 10.1021/acs.macromol.0c0212810.1021/acs.macromol.0c02128 ↗
16. 10.1021/am405138e10.1021/am405138e ↗
17. Fouassier J.-P. · 201210.1002/9783527648245 ↗
18. 10.1021/cm980618w10.1021/cm980618w ↗
19. 10.2494/photopolymer.13.15310.2494/photopolymer.13.153 ↗
20. 10.1039/C4PY00927D10.1039/C4PY00927D ↗
21. 10.1021/acsmacrolett.0c0080910.1021/acsmacrolett.0c00809 ↗
22. 10.1021/acs.macromol.9b0264810.1021/acs.macromol.9b02648 ↗
23. 10.1021/ma501366f10.1021/ma501366f ↗
24. 10.1021/acsmacrolett.8b0043510.1021/acsmacrolett.8b00435 ↗
25. 10.1002/anie.20181011810.1002/anie.201810118 ↗
26. 10.1016/j.jphotochem.2005.07.01910.1016/j.jphotochem.2005.07.019 ↗
27. 10.1021/cr300177k10.1021/cr300177k ↗
28. 10.1126/scitranslmed.300233110.1126/scitranslmed.3002331 ↗
29. 10.1021/acs.biomac.2c0081110.1021/acs.biomac.2c00811 ↗
30. 10.1021/acsmacrolett.5b0092310.1021/acsmacrolett.5b00923 ↗
31. 10.1039/D0PY01373K10.1039/D0PY01373K ↗
32. 10.1021/acs.joc.7b0272910.1021/acs.joc.7b02729 ↗
33. 10.1002/anie.20180582710.1002/anie.201805827 ↗
34. 10.1002/cptc.20200023610.1002/cptc.202000236 ↗
35. 10.1038/s41467-022-27973-x10.1038/s41467-022-27973-x ↗
36. 10.1021/jo401379g10.1021/jo401379g ↗
37. 10.1021/acs.jpcc.6b0442610.1021/acs.jpcc.6b04426 ↗
38. 10.1016/j.catcom.2011.09.00710.1016/j.catcom.2011.09.007 ↗
39. 10.1021/acs.orglett.0c0011810.1021/acs.orglett.0c00118 ↗
40. 10.1021/acs.jmedchem.2c0150410.1021/acs.jmedchem.2c01504 ↗
41. 10.1002/ejoc.20160105410.1002/ejoc.201601054 ↗
42. 10.1039/C5CS00030K10.1039/C5CS00030K ↗
43. 10.1002/anie.20070207010.1002/anie.200702070 ↗
44. 10.1039/c3ob42554a10.1039/c3ob42554a ↗
45. 10.1021/jacs.9b1321910.1021/jacs.9b13219 ↗
46. 10.1002/ejoc.20160023810.1002/ejoc.201600238 ↗
47. 10.1039/c8pp00113h10.1039/c8pp00113h ↗
48. 10.1002/cptc.20210025010.1002/cptc.202100250 ↗
49. 10.1021/jacs.8b0404010.1021/jacs.8b04040 ↗
50. 10.1021/acs.chemrev.0c0066310.1021/acs.chemrev.0c00663 ↗
51. 10.3390/chemistry301001810.3390/chemistry3010018 ↗
52. 10.1021/jacs.9b0903410.1021/jacs.9b09034 ↗
53. 10.1021/jacs.7b0853210.1021/jacs.7b08532 ↗
54. 10.1021/jacs.0c0713610.1021/jacs.0c07136 ↗
55. 10.1039/C9CC07199G10.1039/C9CC07199G ↗
56. 10.1021/jacs.5b0129710.1021/jacs.5b01297 ↗
57. 10.1039/B602797K10.1039/B602797K ↗
58. 10.1002/anie.20211307610.1002/anie.202113076 ↗