Synthesis of Hollow Silica Nanotubes from Linear Metallosupramolecular Polyelectrolytes and Their Application as Catalyst Supports for Hydrogenation
Source abstract
Abstract
In this study, we report a facile templating method to construct hollow silica nanotubes. In particular, bis-terpyridine is used to coordinate metal ions to form polymeric bis-terpyridine–metal complexes that further self-assemble into tubular organogels in the presence of cetyltrimethylammonium bromide. The following silica deposition on organogels and subsequent calcination give metal oxide-doped hollow silica nanotubes (MxOy-HSNs). Facilitated by the high coordination stability constants of bis-terpyridine with metal ions, a series of metal ions, such as Fe, Ni, Cu, and Zn, could be used to form polymeric bis-terpyridine–metal complexes. The supported Pt/FexOy-HSNs exhibit good catalytic performance for hydrogenation of a series of substituted nitrobenzenes, showing that the obtained MxOy-HSNs could be used as catalyst supports due to their good textural properties.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Mesoporous Materials and Catalysis · Nanomaterials for catalytic reactions · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Shanghai Key Laboratory of Multiphase Materials Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China
Funding
National Natural Science Foundation of China
References (46)
Show source-provided references
1. 10.1002/pen.2532810.1002/pen.25328 ↗
2. 10.1021/ja077272n10.1021/ja077272n ↗
3. 10.1021/ma102859210.1021/ma1028592 ↗
4. 10.1021/jp106685q10.1021/jp106685q ↗
5. 10.1021/acs.molpharmaceut.7b0010610.1021/acs.molpharmaceut.7b00106 ↗
6. 10.3390/pharmaceutics1111057110.3390/pharmaceutics11110571 ↗
7. 10.1002/advs.20200149210.1002/advs.202001492 ↗
8. 10.1021/nl902058c10.1021/nl902058c ↗
9. 10.1021/am101051v10.1021/am101051v ↗
10. 10.1021/jp711754h10.1021/jp711754h ↗
11. 10.1039/c3cc41913d10.1039/c3cc41913d ↗
12. 10.1021/acsami.5b0570510.1021/acsami.5b05705 ↗
13. 10.1021/nl015613410.1021/nl0156134 ↗
14. 10.1021/nl015622c10.1021/nl015622c ↗
15. 10.1002/(SICI)1521-4095(200006)12:11<839::AID-ADMA839>3.0.CO;2-910.1002/(SICI)1521-4095(200006)12:11<839::AID-ADMA839>3.0.CO;2-9 ↗
16. 10.1021/cm703698p10.1021/cm703698p ↗
17. 10.1039/b010189n10.1039/b010189n ↗
18. 10.1021/cm703304r10.1021/cm703304r ↗
19. 10.1021/am300469r10.1021/am300469r ↗
20. 10.1016/j.jcis.2009.03.09110.1016/j.jcis.2009.03.091 ↗
21. 10.1016/j.jcrysgro.2005.04.08210.1016/j.jcrysgro.2005.04.082 ↗
22. 10.1021/ja049494g10.1021/ja049494g ↗
23. 10.1021/ja108720w10.1021/ja108720w ↗
24. 10.1021/cm062512410.1021/cm0625124 ↗
25. 10.1021/am201024w10.1021/am201024w ↗
26. 10.1021/cm034356w10.1021/cm034356w ↗
27. 10.1002/adfm.20070059310.1002/adfm.200700593 ↗
28. 10.1021/cm703674d10.1021/cm703674d ↗
29. 10.1021/la203196a10.1021/la203196a ↗
30. 10.1021/jp066644w10.1021/jp066644w ↗
31. 10.1021/cm300312g10.1021/cm300312g ↗
32. 10.1021/jp200515s10.1021/jp200515s ↗
33. 10.1021/jp106690q10.1021/jp106690q ↗
34. 10.1002/adma.20030651810.1002/adma.200306518 ↗
35. 10.1021/acs.inorgchem.5b0293110.1021/acs.inorgchem.5b02931 ↗
36. 10.1021/acsami.0c1826710.1021/acsami.0c18267 ↗
37. 10.1021/acscatal.0c0059110.1021/acscatal.0c00591 ↗
38. 10.1021/acssensors.1c0137410.1021/acssensors.1c01374 ↗
39. 10.1021/j100839a01410.1021/j100839a014 ↗
40. 10.1039/C2RA21918B10.1039/C2RA21918B ↗
41. 10.1021/ja808278s10.1021/ja808278s ↗
42. 10.1021/acs.inorgchem.5b0293110.1021/acs.inorgchem.5b02931 ↗
43. 10.1016/0021-9517(88)90195-910.1016/0021-9517(88)90195-9 ↗
44. 10.1021/ac60353a05010.1021/ac60353a050 ↗
45. 10.1016/0039-6028(95)00336-310.1016/0039-6028(95)00336-3 ↗
46. 10.1088/0022-3719/3/2/01010.1088/0022-3719/3/2/010 ↗