3D Open-Framework Vanadoborate as a Highly Effective Heterogeneous Pre-catalyst for the Oxidation of Alkylbenzenes
Source abstract
Abstract
Three three-dimensional (3D) open-framework vanadoborates, denoted as SUT-6-Zn, SUT-6-Mn, and SUT-6-Ni, were synthesized using diethylenetriamine as a template. SUT-6-Zn, SUT-6-Mn, and SUT-6-Ni are isostructural and built from (VO) 12 O 6 B 18 O 36 (OH) 6 clusters bridged by ZnO 5, MnO 6, and NiO 6 polyhedra, respectively, to form the 3D frameworks. SUT-6 is the first vanadoborate with a 3D framework. The framework follows a semiregular hxg net topology with a 2-fold interpenetrated diamond-like channel system. The amount of template used in the synthesis played an important role in the dimensionality of the resulting vanadoborate structures. A small amount of diethylenetriamine led to the formation of this first 3D vanadoborate framework, while an increased amount of diethylenetriamine resulted in vanadoborates with zero-dimensional (0D) and one-dimensional (1D) structures. SUT-6-Zn was proved to be an efficient heterogeneous precatalyst for the oxidation of alkylbenzenes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Polyoxometalates: Synthesis and Applications · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials and Environmental Chemistry, Stockholm University, SE-106 91 Stockholm, Sweden
Faculty of Material Science and Chemistry, China University of Geosciences, 430074 Wuhan, China
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, SE-106 91 Stockholm, Sweden
College of Chemistry and Molecular Engineering, Peking University, 100871 Beijing, China
References (51)
Show source-provided references
1. Maspoch D. · Chem. Soc. Rev. · 2007 · 36 · 77010.1039/b501600m ↗
2. Wilson S. T. · J. Am. Chem. Soc. · 1982 · 104 · 114610.1021/ja00368a062 ↗
3. Lok B. M. · J. Am. Chem. Soc. · 1984 · 106 · 609310.1021/ja00332a064 ↗
4. Cheetham A. K. · Angew. Chem., Int. Ed. · 1999 · 38 · 326810.1002/(SICI)1521-3773(19991115)38:22<3268::AID-ANIE3268>3.0.CO;2-U ↗
5. Christensen K. E. · Cryst. Rev. · 2010 · 16 · 9110.1080/08893110903428043 ↗
6. Natarajan S. · Angew. Chem., Int. Ed. · 2008 · 47 · 479810.1002/anie.200701404 ↗
7. Huang S. L. · Inorg. Chem. · 2011 · 50 · 992110.1021/ic2013478 ↗
8. Zhou J. · Chem.—Eur. J. · 2010 · 16 · 1325310.1002/chem.201001434 ↗
9. Wang X. Q. · J. Am. Chem. Soc. · 2002 · 124 · 781210.1021/ja020354l ↗
10. Tripathi A. · J. Am. Chem. Soc. · 2003 · 125 · 1052810.1021/ja0365173 ↗
11. Soghomonian V. · Angew. Chem., Int. Ed. · 1993 · 32 · 61010.1002/anie.199306101 ↗
12. Leithall R. M. · J. Am. Chem. Soc. · 2013 · 135 · 291510.1021/ja3119064 ↗
13. Rijssenbeek J. T. · Angew. Chem., Int. Ed. · 1997 · 36 · 100810.1002/anie.199710081 ↗
14. Cai Q. H. · J. Chem. Crystallogr. · 2008 · 38 · 32110.1007/s10870-008-9325-y ↗
15. Liu X. · J. Solid State Chem. · 2013 · 201 · 7910.1016/j.jssc.2013.02.021 ↗
16. Wu M. M. · Chem. Commun. · 2005 · 14 · 1827
17. Warren C. J. · Inorg. Chem. Acta · 1998 · 282 · 12310.1016/S0020-1693(98)00187-X ↗
18. Yamase T. · J. Chem. Soc., Dalton Trans. · 1997 · 246310.1039/a700916j ↗
19. Warren C. J. · Inorg. Chem. · 1998 · 37 · 114010.1021/ic971452o ↗
20. Kareen B. · Inorg. Chim. Acta · 2011 · 367 · 2110.1016/j.ica.2010.11.045 ↗
21. Hermosilla-Ibanez P. · CrystEngComm · 2012 · 14 · 560410.1039/c2ce25436k ↗
22. Sun Y. Q. · Dalton Trans. · 2012 · 41 · 577410.1039/c2dt00018k ↗
23. Williams I. D. · Contemp. Boron Chem. · 2000 · 10410.1039/9781847550644-00104 ↗
24. Zhou J. · RSC Adv. · 2012 · 2 · 1093710.1039/c2ra21635c ↗
25. Crysalis Sofware System, version 171.35.19; Xcalibur CCD System;Oxford Diffraction Ltd.:Yarnton, U.K., 2011.
26. aSheldrick, G. M.SHELXS-97, Program for Solution of Crystal Structures;University of Göttingen:Germany, 1997;
27. Sheldrick G. M. · Acta Crystallogr., Sect. A · 2008 · 64 · 11210.1107/S0108767307043930 ↗
28. Blatov V. · IUCr CompComm Newsletter · 2006 · 7 · 4
29. Ewald B. · Z. Anorg. Allg. Chem. · 2007 · 633 · 151710.1002/zaac.200700232 ↗
30. Liu X. · J. Clust. Sci. · 2011 · 22 · 6510.1007/s10876-011-0359-5 ↗
31. Friedrichs O. D. · Acta Crystallogr., Sect. A · 2003 · 59 · 51510.1107/S0108767303017100 ↗
32. Liu C. S. · Chem. Commun. · 2012 · 48 · 745910.1039/c2cc31905e ↗
33. Yuan N. · CrystEngComm · 2011 · 13 · 595110.1039/c1ce05154g ↗
34. Zhou J. · Inorg. Chem. Commun. · 2012 · 25 · 5110.1016/j.inoche.2012.07.050 ↗
35. Duan W. J. · J. Solid State Chem. · 2007 · 180 · 187510.1016/j.jssc.2007.04.016 ↗
36. Zhang L. R. · J. Solid State Chem. · 1999 · 148 · 45010.1006/jssc.1999.8478 ↗
37. Liu X. · Z. Naturforsch., B: Chem. Sci. · 2011 · 66
38. Xia J.-B. · Chem. Sci. · 2012 · 3 · 224010.1039/c2sc20178j ↗
39. Yang X.-L. · J. Am. Chem. Soc. · 2012 · 134 · 1063810.1021/ja303728c ↗
40. Zou C. · J. Am. Chem. Soc. · 2012 · 134 · 8710.1021/ja209196t ↗
41. Aguadero A. · Angew. Chem., Int. Ed. · 2011 · 50 · 655710.1002/anie.201007941 ↗
42. Dhakshinamoorthy A. · Chem.—Eur. J. · 2011 · 17 · 625610.1002/chem.201002664 ↗
43. Ghiaci M. · Catal. Commun. · 2010 · 11 · 69410.1016/j.catcom.2010.01.023 ↗
44. Yu F. · Dalton Trans. · 2010 · 39 · 758810.1039/c0dt00322k ↗
45. Singh A. P. · Catal. Lett. · 2009 · 132 · 49210.1007/s10562-009-0121-x ↗
46. Mohapatra S. K. · J. Catal. · 2007 · 249 · 39410.1016/j.jcat.2007.04.017 ↗
47. Radhika T. · Catal. Commun. · 2007 · 8 · 15010.1016/j.catcom.2006.05.033 ↗
48. Zhang J.-L. · Chem.—Eur. J. · 2006 · 12 · 302010.1002/chem.200501510 ↗
49. Bhoware S. S. · J. Mol. Catal. A: Chem. · 2006 · 255 · 12310.1016/j.molcata.2006.03.072 ↗
50. Burri E. · Chem.—Eur. J. · 2005 · 11 · 505510.1002/chem.200500375 ↗
51. Khenkin A. M. · J. Am. Chem. Soc. · 2004 · 126 · 635610.1021/ja031710i ↗