journal article·2022-05-11

Catalytic Chiral Photochemistry Sensitized by Chiral Hosts-Grafted Upconverted Nanoparticles

Ming Rao, Chunying Fan, Jiecheng Ji, Wenting Liang, Lingling Wei, Dongjing Zhang, Zhiqiang Yan, Wanhua Wu, Cheng Yang

ACS Applied Materials & Interfaces· Volume 14· Issue 18
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Abstract

Singlet chiral photocatalysis is highly challenging. Herein, we report fluorescence resonance energy transfer (FRET)-based chiral photocatalysis with γ-cyclodextrin (CD)-grafted lanthanide-doped upconverted nanoparticles (UCNP). The CD-modified UCNP strongly emits in the UV wavelength region upon excitation with a 980 nm laser, which selectively sensitizes the photosubstrates complexed by CD on the surface of UCNP through FRET. Therefore, enantiodifferentiating photocyclodimerization of anthracene or naphthalene derivatives sensitized by the CD-modified UCNP gives photoproducts in good enantioselectivity even in the presence of a catalytic amount of CD-modified UCNP. Moreover, the photocatalysts are readily separated and could be reused for at least six cycles without decreasing the enantioselectivity.
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Research context

OpenAlex topics: Radical Photochemical Reactions · Molecular Sensors and Ion Detection · Surface Chemistry and Catalysis

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

Affiliations

Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610064, China

School of Pharmacy, Health Science Center, Xi’an Jiaotong University, Xi’an 710061, China

Institute of Environmental Science, Department of Chemistry, Shanxi University, Taiyuan 030006, China

Funding

Central University Basic Research Fund of China · Department of Science and Technology of Sichuan Province · National Natural Science Foundation of China

References (60)

Show source-provided references
1. 10.1038/s41929-020-00528-310.1038/s41929-020-00528-3 ↗
2. 10.1021/acs.orglett.8b0052010.1021/acs.orglett.8b00520 ↗
3. 10.1016/j.gresc.2021.03.00510.1016/j.gresc.2021.03.005 ↗
4. 10.1021/acs.chemrev.1c0046710.1021/acs.chemrev.1c00467 ↗
5. 10.1021/acs.chemrev.1c0099310.1021/acs.chemrev.1c00993 ↗
6. 10.1038/nature0395510.1038/nature03955 ↗
7. 10.1021/acs.chemrev.1c0038810.1021/acs.chemrev.1c00388 ↗
8. 10.1021/acs.chemrev.1c0027210.1021/acs.chemrev.1c00272 ↗
9. 10.1038/s41586-018-0755-110.1038/s41586-018-0755-1 ↗
10. 10.1016/j.cclet.2019.09.00910.1016/j.cclet.2019.09.009 ↗
11. 10.1126/science.124480910.1126/science.1244809 ↗
12. 10.1039/c3cs60117j10.1039/c3cs60117j ↗
13. Turro N. J. · 1969 · 1
14. Turro N. J. · 2009
15. 10.1038/338264a010.1038/338264a0 ↗
16. 10.1021/ja202020x10.1021/ja202020x ↗
17. 10.1021/jacs.7b1208510.1021/jacs.7b12085 ↗
18. 10.1021/acs.chemrev.6b0004010.1021/acs.chemrev.6b00040 ↗
19. 10.1039/C3CS60339C10.1039/C3CS60339C ↗
20. 10.1016/j.cclet.2013.03.02810.1016/j.cclet.2013.03.028 ↗
21. 10.1021/jacs.9b0199310.1021/jacs.9b01993 ↗
22. 10.31635/ccschem.021.20210103610.31635/ccschem.021.202101036 ↗
23. 10.1021/ja016238k10.1021/ja016238k ↗
24. 10.1021/ar020269i10.1021/ar020269i ↗
25. 10.1002/ange.20090160310.1002/ange.200901603 ↗
26. 10.1039/C5CC09107A10.1039/C5CC09107A ↗
27. 10.1016/j.jphotochem.2015.10.02310.1016/j.jphotochem.2015.10.023 ↗
28. 10.1021/acs.orglett.7b0005710.1021/acs.orglett.7b00057 ↗
29. 10.3762/bjoc.8.14910.3762/bjoc.8.149 ↗
30. 10.1039/C8CS00002F10.1039/C8CS00002F ↗
31. 10.1039/C4CS00155A10.1039/C4CS00155A ↗
32. 10.1038/nphoton.2015.14210.1038/nphoton.2015.142 ↗
33. 10.1021/acsphotonics.8b0011210.1021/acsphotonics.8b00112 ↗
34. 10.1038/s41566-019-0528-x10.1038/s41566-019-0528-x ↗
35. 10.1002/anie.20110137410.1002/anie.201101374 ↗
36. 10.1021/jacs.5b0150410.1021/jacs.5b01504 ↗
37. 10.1038/ncomms983210.1038/ncomms9832 ↗
38. 10.1126/science.aaq114410.1126/science.aaq1144 ↗
39. 10.1021/jacs.6b0934910.1021/jacs.6b09349 ↗
40. 10.1016/j.chempr.2021.03.00810.1016/j.chempr.2021.03.008 ↗
41. 10.1002/anie.20210529710.1002/anie.202105297 ↗
42. 10.1021/acs.inorgchem.0c0004310.1021/acs.inorgchem.0c00043 ↗
43. 10.1038/s41467-020-18223-z10.1038/s41467-020-18223-z ↗
44. 10.1038/nprot.2014.11110.1038/nprot.2014.111 ↗
45. 10.4028/www.scientific.net/AMR.1095.6310.4028/www.scientific.net/AMR.1095.63 ↗
46. 10.1016/j.saa.2013.09.03610.1016/j.saa.2013.09.036 ↗
47. 10.1016/S0141-3910(00)00084-710.1016/S0141-3910(00)00084-7 ↗
48. 10.1002/anie.20191610310.1002/anie.201916103 ↗
49. 10.1021/acs.orglett.0c0384810.1021/acs.orglett.0c03848 ↗
50. 10.1111/php.1299310.1111/php.12993 ↗
51. 10.1021/la904629a10.1021/la904629a ↗
52. 10.1351/PAC-CON-10-10-0410.1351/PAC-CON-10-10-04 ↗
53. 10.1021/jacs.6b0559810.1021/jacs.6b05598 ↗
54. 10.1021/ja503290810.1021/ja5032908 ↗
55. 10.1039/C3PP50255D10.1039/C3PP50255D ↗
56. 10.1021/acs.joc.5b0290910.1021/acs.joc.5b02909 ↗
57. 10.1021/jacs.5b0977510.1021/jacs.5b09775 ↗
58. 10.1073/pnas.43.1.13310.1073/pnas.43.1.133 ↗
59. 10.1016/1010-6030(92)85056-Z10.1016/1010-6030(92)85056-Z ↗
60. 10.1021/acs.orglett.0c0119410.1021/acs.orglett.0c01194 ↗