Highly Efficient Synthesis of p-Benzoquinones Catalyzed by Robust Two-Dimensional POM-Based Coordination Polymers
Source abstract
Abstract
Selective oxidation of alkyl-substituted phenols offers efficient access to p-benzoquinones (BQs) that serve as key components for synthesizing biologically active compounds, but rational manufacture of efficient recyclable catalysts for such a reaction remains a severe challenge. Herein, two crystalline 2D polyoxometalate-based coordination polymers (POMCPs), formulated as H3[CuI3(L)3]2[PM12O40]·xH2O (M = Mo, x = 4 for 1; M = W, x = 6 for 2; and HL = 4-(1H-tetazol-5-yl)pyridine), are prepared by a mineralizer-assisted one-step synthesis strategy and explored as heterogeneous catalysts for p-BQs synthesis. Both compounds have been characterized through elemental analysis, EDS analysis, infrared spectroscopy, UV–vis diffuse reflectance spectrum, EPR, XPS, BET, single-crystal, and powder X-ray diffraction. Single-crystal X-ray diffraction analysis indicates that both 1 and 2 exhibit an interesting 2D sheet structure composed of 2-connected Keggin type anions [PM12O40]3– and hexa-nuclear {CuI6(HL)6} cluster-based metal–organic chains via Cu···O interactions. When used as catalysts, POMCPs 1 and 2 have excellent catalytic activities in the selective oxidation of substituted phenols to p-BQs with H2O2. Notedly, in the model reaction from 2,3,6-trimethylphenol (TMP) to the vitamin E key intermediate trimethyl-p-benzoquinone (TMBQ), the catalytic activities expressed by turnover frequency (TOF) of 1 and 2 can reach an unprecedented 2400 and 2000 h–1, respectively, at close to 100% TMBQ yield. The truly heterogeneous nature, stability, and structural integrity of both catalysts were ascertained by FTIR, PXRD techniques, and the following cycles. Mechanism studies reveal that both catalysts can involve a dual reaction pathway through a heterolytic oxygen atom transfer mechanism and homolytic radical mechanism. Moreover, the 2D POMCPs with highly accessible bilateral active sites and efficient mass transfer efficiency possess superior catalytic performance to their analogous 3D species.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Polyoxometalates: Synthesis and Applications · Advanced Nanomaterials in Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Engineering, Dalian University of Technology, Dalian 116023, People’s Republic of China
Funding
Ministry of Education of the People's Republic of China · Natural Science Foundation of Liaoning Province · National Natural Science Foundation of China
References (70)
Show source-provided references
1. Skancke A. · 1988 · 1
2. 10.1016/j.apcata.2004.08.02810.1016/j.apcata.2004.08.028 ↗
3. 10.1002/anie.20120588610.1002/anie.201205886 ↗
4. 10.1038/nature0737110.1038/nature07371 ↗
5. 10.1038/368321a010.1038/368321a0 ↗
6. Isshiki, T.; Yui, T.; Uno, H.; Abe, M. Process for the Production of 2,3,5-Trimethylbenzoquinone. European Patent EP 0127888 B1, 1987.
7. Bernhard, B.; Ulrich, H.; Harald, L.; Barbara, J.; Paul, G. Process for the Preparation of 2,3,5-Trimethyl-p-Benzoquinone. European Patent EP 0475272 A2, 1992.
8. 10.1021/ja039196410.1021/ja0391964 ↗
9. 10.1021/acscatal.9b0172310.1021/acscatal.9b01723 ↗
10. 10.1021/acs.inorgchem.9b0242210.1021/acs.inorgchem.9b02422 ↗
11. 10.1021/acs.chemrev.8b0036810.1021/acs.chemrev.8b00368 ↗
12. 10.1016/j.ccr.2015.07.01910.1016/j.ccr.2015.07.019 ↗
13. 10.1016/j.jhazmat.2019.03.00110.1016/j.jhazmat.2019.03.001 ↗
14. 10.1002/cctc.20130106910.1002/cctc.201301069 ↗
15. 10.1002/ejic.20130109810.1002/ejic.201301098 ↗
16. 10.1021/acsami.5b0966310.1021/acsami.5b09663 ↗
17. 10.1021/acscatal.5b0122210.1021/acscatal.5b01222 ↗
18. 10.1021/acsnano.9b0585610.1021/acsnano.9b05856 ↗
19. 10.1021/cr960395y10.1021/cr960395y ↗
20. 10.1002/advs.20190351110.1002/advs.201903511 ↗
21. 10.1021/acsami.9b1669410.1021/acsami.9b16694 ↗
22. 10.1002/anie.20200805410.1002/anie.202008054 ↗
23. 10.1021/acsami.0c1897010.1021/acsami.0c18970 ↗
24. 10.1016/S0040-4039(00)95231-610.1016/S0040-4039(00)95231-6 ↗
25. 10.1016/S1381-1169(99)00328-310.1016/S1381-1169(99)00328-3 ↗
26. 10.1016/j.catcom.2007.04.02610.1016/j.catcom.2007.04.026 ↗
27. 10.1021/cs500738e10.1021/cs500738e ↗
28. 10.1016/j.apcata.2007.10.02510.1016/j.apcata.2007.10.025 ↗
29. 10.1021/acscatal.7b0393310.1021/acscatal.7b03933 ↗
30. 10.1007/s10971-020-05239-610.1007/s10971-020-05239-6 ↗
31. 10.1039/C3CS60404G10.1039/C3CS60404G ↗
32. 10.1039/c0dt00426j10.1039/c0dt00426j ↗
33. 10.1021/acs.inorgchem.7b0156410.1021/acs.inorgchem.7b01564 ↗
34. 10.1016/j.apsusc.2020.14830610.1016/j.apsusc.2020.148306 ↗
35. 10.1038/s41467-018-06938-z10.1038/s41467-018-06938-z ↗
36. 10.1021/acsami.8b1077710.1021/acsami.8b10777 ↗
37. 10.1021/acsami.9b1492810.1021/acsami.9b14928 ↗
38. 10.1039/D0TA04993J10.1039/D0TA04993J ↗
39. 10.1021/acsami.9b1978510.1021/acsami.9b19785 ↗
40. 10.1021/acs.chemmater.0c0044010.1021/acs.chemmater.0c00440 ↗
41. 10.1002/anie.20120850110.1002/anie.201208501 ↗
42. 10.1021/acssuschemeng.9b0269910.1021/acssuschemeng.9b02699 ↗
43. 10.1016/j.mtchem.2018.12.00210.1016/j.mtchem.2018.12.002 ↗
44. 10.1021/acsami.8b2099010.1021/acsami.8b20990 ↗
45. 10.1002/anie.20200712210.1002/anie.202007122 ↗
46. 10.1002/adma.20180340110.1002/adma.201803401 ↗
47. 10.1016/j.ccr.2019.04.00810.1016/j.ccr.2019.04.008 ↗
48. 10.1021/acs.inorgchem.0c0279810.1021/acs.inorgchem.0c02798 ↗
49. 10.1021/cm011725k10.1021/cm011725k ↗
50. 10.1002/asia.20130137810.1002/asia.201301378 ↗
51. 10.1021/acsami.9b0087210.1021/acsami.9b00872 ↗
52. 10.1016/j.jcat.2010.07.01710.1016/j.jcat.2010.07.017 ↗
53. 10.1002/anie.20190560010.1002/anie.201905600 ↗
54. 10.1107/S010876818500206310.1107/S0108768185002063 ↗
55. Byrappa K. · 2013
56. 10.1039/c2cc31667f10.1039/c2cc31667f ↗
57. 10.1021/acsami.7b1730610.1021/acsami.7b17306 ↗
58. 10.1039/c3dt50732g10.1039/c3dt50732g ↗
59. 10.1038/s41929-019-0405-510.1038/s41929-019-0405-5 ↗
60. 10.1002/anie.20170723810.1002/anie.201707238 ↗
61. 10.1039/C8DT01936C10.1039/C8DT01936C ↗
62. 10.1038/s41929-020-00507-810.1038/s41929-020-00507-8 ↗
63. 10.1039/b617162a10.1039/b617162a ↗
64. 10.1002/adsc.20090010910.1002/adsc.200900109 ↗
65. 10.1039/c4cy00313f10.1039/c4cy00313f ↗
66. 10.1039/C3CY00615H10.1039/C3CY00615H ↗
67. 10.1002/adsc.20150084610.1002/adsc.201500846 ↗
68. 10.1002/anie.20170015910.1002/anie.201700159 ↗
69. 10.1021/acscatal.8b0097210.1021/acscatal.8b00972 ↗
70. 10.1021/cr500390v10.1021/cr500390v ↗