Photoactive Metal–Organic Framework for the Reduction of Aryl Halides by the Synergistic Effect of Consecutive Photoinduced Electron-Transfer and Hydrogen-Atom-Transfer Processes
Source abstract
Abstract
Consecutive photoinduced electron transfer (ConPET) has advantages on overcoming the current energetic limitation of visible-light photoredox catalysis for utilizing the energies of two photons in one catalytic cycle. A heterogeneous approach for radical chain reduction of various aryl bromides and chlorides without adding any cocatalyst is introduced by incorporating polyoxometalates (POMs) and amine catalysts into a naphthalenediimide (NDI)-based polymer. CoW-DPNDI–PYI exhibits high activity in the photocatalytic reduction of aryl halides by the synergistic effects of ConPET and hydrogen-atom-transfer (HAT) processes and an enzyme-mimicking CO2 cycloaddition reaction. The ConPET process with N,N′-bis(4-pyridylmethyl)naphthalenediimide (DPNDI) facilitates effective solar energy conversion. POMs and amine catalysts, as efficient HAT catalysts and electron donors, improve the generation of the ConPET process. The success of this work demonstrates the great application of the synergistic effects of ConPET and HAT processes in heterogeneous photocatalysis C–H arylation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Carbon dioxide utilization in catalysis · Chemical Synthesis and Reactions · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Polyoxometalate Chemistry of Henan Province, School of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004, P. R. China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Henan University · Key Scientific Research Project of Henan Higher Education Institutions
References (54)
Show source-provided references
1. 10.1021/acs.chemrev.8b0007710.1021/acs.chemrev.8b00077 ↗
2. 10.1021/acs.accounts.6b0022910.1021/acs.accounts.6b00229 ↗
3. 10.1039/c9sc02000d10.1039/c9sc02000d ↗
4. 10.1002/anie.20170653410.1002/anie.201706534 ↗
5. 10.1126/science.113827510.1126/science.1138275 ↗
6. 10.1002/anie.20120359910.1002/anie.201203599 ↗
7. 10.1021/cs300507a10.1021/cs300507a ↗
8. 10.1021/ja045989u10.1021/ja045989u ↗
9. 10.1002/anie.20120008410.1002/anie.201200084 ↗
10. 10.1002/anie.20160234910.1002/anie.201602349 ↗
11. 10.1126/science.125823210.1126/science.1258232 ↗
12. 10.1016/j.ccr.2018.02.01010.1016/j.ccr.2018.02.010 ↗
13. 10.1021/acs.inorgchem.9b0020610.1021/acs.inorgchem.9b00206 ↗
14. 10.1021/acs.accounts.6b0033910.1021/acs.accounts.6b00339 ↗
15. 10.1021/acscatal.8b0349810.1021/acscatal.8b03498 ↗
16. 10.1038/s41586-018-0366-x10.1038/s41586-018-0366-x ↗
17. 10.1126/science.aac855510.1126/science.aac8555 ↗
18. 10.1126/science.aaf663510.1126/science.aaf6635 ↗
19. 10.1021/acscatal.6b0292310.1021/acscatal.6b02923 ↗
20. 10.1021/acs.accounts.8b0052110.1021/acs.accounts.8b00521 ↗
21. 10.1021/acs.inorgchem.9b0205610.1021/acs.inorgchem.9b02056 ↗
22. 10.1021/ar00092a00210.1021/ar00092a002 ↗
23. 10.1039/c6gc00370b10.1039/c6gc00370b ↗
24. 10.1021/acscatal.7b0358010.1021/acscatal.7b03580 ↗
25. Nguyen P. T. K. · ACS Appl. Mater. Interfaces · 2018 · 10 · 73310.1021/acsami.7b16163 ↗
26. 10.1021/jo800916510.1021/jo8009165 ↗
27. 10.1021/ic901126310.1021/ic9011263 ↗
28. 10.1021/ic00144a00610.1021/ic00144a006 ↗
29. 10.1107/s002188980202211210.1107/s0021889802022112 ↗
30. 10.1021/ja303173n10.1021/ja303173n ↗
31. 10.1038/s41557-018-0172-y10.1038/s41557-018-0172-y ↗
32. 10.1021/jacs.6b0571210.1021/jacs.6b05712 ↗
33. 10.1021/jacs.5b1293110.1021/jacs.5b12931 ↗
34. 10.1039/c2cc37497h10.1039/c2cc37497h ↗
35. 10.1016/j.jcat.2019.06.04010.1016/j.jcat.2019.06.040 ↗
36. 10.1021/acsami.8b0035010.1021/acsami.8b00350 ↗
37. 10.1021/acs.chemmater.7b0110910.1021/acs.chemmater.7b01109 ↗
38. 10.1021/acsami.7b1417910.1021/acsami.7b14179 ↗
39. 10.1039/c2ce06147c10.1039/c2ce06147c ↗
40. 10.1021/ja038926510.1021/ja0389265 ↗
41. 10.1021/jo950933r10.1021/jo950933r ↗
42. 10.1021/jacs.6b0969010.1021/jacs.6b09690 ↗
43. 10.1021/ja408073m10.1021/ja408073m ↗
44. 10.1021/acscatal.7b0335410.1021/acscatal.7b03354 ↗
45. 10.1070/rc1987v056n09abeh00330410.1070/rc1987v056n09abeh003304 ↗
46. 10.1007/s10118-018-2047-510.1007/s10118-018-2047-5 ↗
47. 10.1002/anie.20046044210.1002/anie.200460442 ↗
48. 10.1021/acs.cgd.8b0156410.1021/acs.cgd.8b01564 ↗
49. 10.1002/adsc.20039003510.1002/adsc.200390035 ↗
50. 10.1038/ncomms1000710.1038/ncomms10007 ↗
51. 10.1039/c5sc03694a10.1039/c5sc03694a ↗
52. 10.1021/acscatal.7b0340410.1021/acscatal.7b03404 ↗
53. 10.1021/ie504287910.1021/ie5042879 ↗
54. 10.1021/cm021269f10.1021/cm021269f ↗