MoIV3⋯[O 8 Mo 4 ] 3 Lewis acid–base cluster pairs: highly efficient and stable Lewis catalysis fields frustrated in crystalline nanoclusters
Source abstract
Abstract
By using metal compounds or oxide/organic acid and enhanced reaction temperatures in the controlled solvothermal oxidation of [Mo3O2(MeCO2)6(H2O)3]2+, more interstitial metal atoms were introduced to produce the largest nanoscale MoIV-polyoxomolybdates, [M2@(MoIV3py3)4Mo18Ox]q- (M = Al, V, Mo). Each [H4V2@(MoIV3py3)4Mo18O84]12- (2a) nanocluster is surrounded by 12 [V3Mo12O42] to build a Lewis catalysis field (LCF) composed of MoIV3[O8Mo4]3 Lewis acid-base cluster pairs in the crystalline 2, accounting for the excellent and stable catalysis performance in the hydrazine reduction of nitroarenes to arylamines in varied solvents. The proposed new concept LCF provides a new way of thinking for designed synthesis and real applications of highly efficient LCF catalysts.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Polyoxometalates: Synthesis and Applications · Metal-Organic Frameworks: Synthesis and Applications · Nanocluster Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Structural Chemistry
Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences
Fuzhou
P. R. China
University of Chinese Academy of Sciences
Funding
National Natural Science Foundation of China · Chinese Academy of Sciences
References (50)
Show source-provided references
1. Stephan · Science · 2016 · 354 · aaf722910.1126/science.aaf7229 ↗
2. Lam · Chem. Soc. Rev. · 2018 · 48 · 359210.1039/C8CS00277K ↗
3. Tutusaus · J. Am. Chem. Soc. · 2013 · 135 · 340310.1021/ja400962h ↗
4. Flynn · ACS Catal. · 2013 · 3 · 257410.1021/cs400754w ↗
5. Ma · Chem. Soc. Rev. · 2018 · 47 · 554110.1039/C7CS00691H ↗
6. Yu · Dalton Trans. · 2019 · 48 · 1744510.1039/C9DT04138A ↗
7. Miras · Chem. Soc. Rev. · 2012 · 41 · 740310.1039/c2cs35190k ↗
8. Müller · Chem. Soc. Rev. · 2012 · 41 · 743110.1039/c2cs35169b ↗
9. Nishimoto · J. Am. Chem. Soc. · 2014 · 136 · 904210.1021/ja5032369 ↗
10. Wang · J. Am. Chem. Soc. · 2012 · 134 · 491810.1021/ja2117206 ↗
11. Chen · Nat. Chem. · 2018 · 10 · 104210.1038/s41557-018-0109-5 ↗
12. Wang · Nat. Commun. · 2018 · 9 · 110.1038/s41467-017-02088-w ↗
13. Zheng · J. Am. Chem. Soc. · 2018 · 140 · 259510.1021/jacs.7b11982 ↗
14. Zheng · J. Am. Chem. Soc. · 2019 · 141 · 1347910.1021/jacs.9b04533 ↗
15. Xu · Angew. Chem., Int. Ed. · 2019 · 58 · 110.1002/anie.201813481 ↗
16. Ochoa · Chem. Commun. · 2011 · 47 · 879910.1039/c1cc12782a ↗
17. Chen · Chem. Soc. Rev. · 2019 · 48 · 26010.1039/C8CS00559A ↗
18. Daniel · J. Am. Chem. Soc. · 2009 · 131 · 510110.1021/ja8073648 ↗
19. Spandl · Angew. Chem., Int. Ed. · 2003 · 42 · 116310.1002/anie.200390306 ↗
20. Wang · Chem. Rev. · 2015 · 115 · 489310.1021/cr500390v ↗
21. Li · Nanoscale · 2020 · 12 · 1609110.1039/D0NR04051G ↗
22. Liu · Nanoscale · 2020 · 12 · 1658610.1039/D0NR03951A ↗
23. Song · Chem. Soc. Rev. · 2012 · 41 · 738410.1039/c2cs35143a ↗
24. Liu · Angew. Chem., Int. Ed. · 2018 · 57 · 841610.1002/anie.201803649 ↗
25. Wang · Nanoscale · 2020 · 12 · 570510.1039/C9NR10573E ↗
26. Zhang · Nanoscale · 2020 · 12 · 1084210.1039/D0NR01901A ↗
27. Benaissa · J. Catal. · 2008 · 253 · 24410.1016/j.jcat.2007.11.011 ↗
28. Benaissa · Appl. Catal., A · 2008 · 351 · 8810.1016/j.apcata.2008.09.003 ↗
29. Lin · J. Catal. · 2016 · 341 · 13610.1016/j.jcat.2016.06.008 ↗
30. MacDonald · Chem. Commun. · 2018 · 54 · 109310.1039/C7CC09036F ↗
31. Gumerova · Nat. Rev. Chem. · 2018 · 2 · 011210.1038/s41570-018-0112 ↗
32. Petel · Chem. Commun. · 2020 · 56 · 55510.1039/C9CC08230A ↗
33. Schreiber · J. Am. Chem. Soc. · 2020 · 142 · 991510.1021/jacs.0c03864 ↗
34. Petel · Chem. Sci. · 2019 · 10 · 803510.1039/C9SC02882J ↗
35. Piepgrass · J. Am. Chem. Soc. · 1987 · 109 · 158710.1021/ja00239a058 ↗
36. Smith · Electrochim. Acta · 2008 · 53 · 299410.1016/j.electacta.2007.11.027 ↗
37. D. T. Richens , The Chemistry of Aqua Ions , John Wiley & Sons , Chichester , 1997
38. Cotton · Inorg. Chem. · 1984 · 23 · 367110.1021/ic00190a052 ↗
39. Chen · Chem. Commun. · 2013 · 49 · 588310.1039/c3cc41954a ↗
40. Bino · J. Am. Chem. Soc. · 1978 · 100 · 525210.1021/ja00484a080 ↗
41. Xu · Dalton Trans. · 2018 · 47 · 321810.1039/C7DT04309K ↗
42. Luo · Catal. Sci. Technol. · 2019 · 9 · 6510.1039/C8CY01771A ↗
43. Luo · Dalton Trans. · 2019 · 48 · 689210.1039/C9DT00983C ↗
44. Xu · J. Chem. Soc., Chem. Commun. · 1993 · 1507
45. Xu · Chem. – Eur. J. · 1997 · 3 · 22610.1002/chem.19970030210 ↗
46. Xu · J. Chem. Soc., Dalton Trans. · 1994 · 209910.1039/DT9940002099 ↗
47. Xu · Inorg. Chem. · 1996 · 35 · 509710.1021/ic951542y ↗
48. H. J. Arpe , Industrial Organic Chemistry , Wiley-VCH , Weinheim , 5th edn, 2010
49. Modern Reduction Methods , ed. P. G. Andersson and I. J. Munslow , Wiley-VCH Verlag GmbH & Co. KGaA , Weinheim , 2008
50. Catalytic Hydrogenation , ed. L. Cerveny , Elsevier , Amsterdam , 1986