journal article·2024-08Open access

Spatiotemporal Release of Singlet Oxygen in Low Molecular Weight Organo‐Gels Upon Thermal or Photochemical External Stimuli

Emil Sandelin, Leonard Schilling, Ekata Saha, Andrea Ruiu, Richard Neutze, Henrik Sundén, Carl‐Johan Wallentin

Small· Volume 20· Issue 35

Abstract

Abstract The first example of a material capable of spatiotemporal catch and release of singlet oxygen (1O2) in gel phase is presented. Several low molecular weight organogelators based around an oxotriphenylhexanoate (OTHO) core are developed and optimized with regard to; their gelation properties, and ability of releasing 1O2 upon thermal and/or photochemical external stimuli, in both gel phase and solution. Remarkably, reversible phase transitioning between the gel and solution phase are also demonstrated. Taken together two complementary modes of releasing 1O2, one thermally controlled over time, and one rapid release by means of photochemical stimuli is disclosed. These findings represent the first phase reversible system where function and aggregation properties can be controlled independently, and thus pave the way for novel applications in material sciences as well as in life sciences.
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Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Porphyrin and Phthalocyanine Chemistry · Luminescence and Fluorescent Materials

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

Affiliations

Department of Chemistry and Molecular Biology University of Gothenburg Gothenburg SE‐413 90 Sweden

Centre for Analysis and Synthesis Department of Chemistry Lund University Lund SE‐221 00 Sweden

Funding

Olle Engkvists Stiftelse · Stiftelsen Sigurd and Elsa Goljes Minne · Wenner-Gren Stiftelserna · Vetenskapsrådet · HORIZON EUROPE European Research Council · Adlerbertska Research Foundation

References (38)

Show source-provided references
1. 10.1039/C8OB00504D10.1039/C8OB00504D ↗
2. 10.1016/j.ccr.2020.21354110.1016/j.ccr.2020.213541 ↗
3. 10.1080/1040841X.2018.146787610.1080/1040841X.2018.1467876 ↗
4. 10.1002/wnan.156010.1002/wnan.1560 ↗
5. 10.1002/jbio.20160005510.1002/jbio.201600055 ↗
6. 10.3322/caac.2011410.3322/caac.20114 ↗
7. 10.3390/pharmaceutics1502033010.3390/pharmaceutics15020330 ↗
8. 10.3390/biom1201008110.3390/biom12010081 ↗
9. 10.1039/c3cc42217h10.1039/c3cc42217h ↗
10. 10.1002/anie.20200244610.1002/anie.202002446 ↗
11. 10.2147/HP.S9341310.2147/HP.S93413 ↗
12. 10.1038/s41427‐021‐00303‐110.1038/s41427‐021‐00303‐1 ↗
13. 10.1039/D0CC06031C10.1039/D0CC06031C ↗
14. 10.1021/jacs.9b0195810.1021/jacs.9b01958 ↗
15. 10.1038/s41467‐018‐06392‐x10.1038/s41467‐018‐06392‐x ↗
16. 10.1021/ja051701510.1021/ja0517015 ↗
17. 10.1002/anie.20070044310.1002/anie.200700443 ↗
18. 10.1039/C8SC03127D10.1039/C8SC03127D ↗
19. 10.1002/anie.20151006410.1002/anie.201510064 ↗
20. 10.1039/C8PY00289D10.1039/C8PY00289D ↗
21. 10.1002/smll.20220236910.1002/smll.202202369 ↗
22. 10.1039/C9CC06231A10.1039/C9CC06231A ↗
23. 10.1063/5.00210.1063/5.002 ↗
24. 10.1002/chem.20180063510.1002/chem.201800635 ↗
25. 10.1039/C9CC08994B10.1039/C9CC08994B ↗
26. 10.3390/catal504205210.3390/catal5042052 ↗
27. 10.1021/acs.iecr.1c0191410.1021/acs.iecr.1c01914 ↗
28. 10.1002/cptc.20170023510.1002/cptc.201700235 ↗
29. 10.1021/ja035828a10.1021/ja035828a ↗
30. 10.1021/j100412a05510.1021/j100412a055 ↗
31. 10.1021/ct500909a10.1021/ct500909a ↗
32. 10.1039/b719637g10.1039/b719637g ↗
33. 10.1021/acs.joc.7b0176510.1021/acs.joc.7b01765 ↗
34. 10.1002/cptc.20210009710.1002/cptc.202100097 ↗
35. 10.1021/jacs.2c0209610.1021/jacs.2c02096 ↗
36. 10.1039/C6SM01779G10.1039/C6SM01779G ↗
37. 10.1039/c2cc37249e10.1039/c2cc37249e ↗
38. 10.1021/ja306056x10.1021/ja306056x ↗