Template-Free Synthesis of a Porous Organic–inorganic Hybrid Tin(IV) Phosphonate and Its High Catalytic Activity for Esterification of Free Fatty Acids
Source abstract
Abstract
Here we have synthesized an organic-inorganic hybrid mesoporous tin phosphonate monolith (MLSnP-1) with crystalline pore walls by a template-free sol-gel route. N2 sorption analysis shows Brunauer-Emmett-Teller (BET) surface area of 347 m2 g(-1). Wide-angle powder X-ray diffraction (PXRD) pattern shows few broad diffraction peaks indicating crystalline pore wall of the material. High-resolution transmission electron microscopic (HR TEM) image further reveals the crystal fringes on the pore wall. Framework bonding and local environment around phosphorus and carbon were examined by Fourier transform infrared (FT IR) spectroscopy and solid-state MAS NMR spectroscopy. The material exhibits remarkable catalytic activity for esterification of long chain fatty acids under mild reaction conditions at room temperature.
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Research context
OpenAlex topics: Chemical Synthesis and Reactions · Polyoxometalates: Synthesis and Applications · Metal-Organic Frameworks: Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, India
Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan
References (42)
Show source-provided references
1. Horike S. · J. Am. Chem. Soc. · 2008 · 130 · 585410.1021/ja800669j ↗
2. Mal N. K. · Nature · 2003 · 421 · 35010.1038/nature01362 ↗
3. Ren S. · Nano Lett. · 2011 · 11 · 399810.1021/nl202435t ↗
4. Chang C.-C. · Chem. Mater. · 2002 · 14 · 424210.1021/cm0202310 ↗
5. Dutta A. · ChemPhysChem · 2012 · 13 · 321810.1002/cphc.201200096 ↗
6. Dutta A. · Chem.—Eur. J. · 2012 · 18 · 1337210.1002/chem.201201350 ↗
7. Dutta A. · Chem. Commun. · 2012 · 48 · 673810.1039/c2cc32298f ↗
8. Dutta A. · Microporous Mesoporous Mater. · 2012 · 155 · 20810.1016/j.micromeso.2012.01.017 ↗
9. Cabrera K. · J. Sep. Sci. · 2004 · 27 · 84310.1002/jssc.200401827 ↗
10. Legido-Quigley C. · Electrophoresis · 2003 · 24 · 91710.1002/elps.200390136 ↗
11. Drisko G. L. · ACS Appl. Mater. Interfaces · 2012 · 4 · 412310.1021/am300880q ↗
12. Kanamori K. · Chem. Soc. Rev. · 2011 · 40 · 75410.1039/C0CS00068J ↗
13. Peters E. C. · Adv. Mater. · 1999 · 11 · 116910.1002/(SICI)1521-4095(199910)11:14<1169::AID-ADMA1169>3.0.CO;2-6 ↗
14. Haughton L. · J. Chem. Soc., Perkin Trans. 1 · 1999 · 264510.1039/a808299e ↗
15. Zhang H. · Chem. Mater. · 2004 · 16 · 424510.1021/cm0492944 ↗
16. Kido Y. · Chem. Mater. · 2012 · 24 · 207110.1021/cm300495j ↗
17. Ma T.-Y. · Chem. Commun. · 2010 · 46 · 232510.1039/b920964f ↗
18. Ohtani B. · J. Phys. Chem. B · 1997 · 101 · 374610.1021/jp962702+ ↗
19. Smatt J.-H. · Chem. Commun. · 2004 · 218810.1039/B405208K ↗
20. Kirumakki S. · J. Mater. Chem. · 2009 · 19 · 259310.1039/b818618a ↗
21. Kirumakki S. · Chem. Commun. · 2008 · 555610.1039/b807938b ↗
22. Subbiah A. · J. Am. Chem. Soc. · 2005 · 127 · 1082610.1021/ja052472p ↗
23. Cardoso A. L. · Energy Fuels · 2009 · 23 · 171810.1021/ef800639h ↗
24. Pramanik M. · Catal. Sci. Technol. · 2012 · 2 · 61310.1039/c2cy00352j ↗
25. Hudson M. J. · J. Mater. Chem. · 1991 · 1 · 37510.1039/jm9910100375 ↗
26. Norris, C. E.; Quideau, S. A.; Landhausser, S. M.; Bernard, G. M.; Wasylishen, R. E.,Sci. Rep. 2012, 2.10.1038/srep00719 ↗
27. Smått J.-H. · Chem. Mater. · 2003 · 15 · 235410.1021/cm0213422 ↗
28. Inagaki S. · Nature · 2002 · 416 · 30410.1038/416304a ↗
29. Schmidt R. · Microporous Mater. · 1995 · 3 · 44310.1016/0927-6513(94)00055-Z ↗
30. Patra A. K. · ACS Appl. Mater. Interfaces · 2012 · 4 · 502210.1021/am301394u ↗
31. Kaneko K. · Carbon · 1992 · 30 · 107510.1016/0008-6223(92)90139-N ↗
32. Vasudevan P. T. · J. Ind. Microbiol. Biotechnol. · 2008 · 35 · 42110.1007/s10295-008-0312-2 ↗
33. Stöveken T. · Angew. Chem., Int. Ed. · 2008 · 47 · 368810.1002/anie.200705265 ↗
34. Gang L. · New J. Chem. · 2007 · 31 · 34810.1039/b615448d ↗
35. Das S. K. · ACS Catal. · 2011 · 1 · 49310.1021/cs200005z ↗
36. Pirez C. · ACS Catal. · 2012 · 2 · 160710.1021/cs300161a ↗
37. Dhainaut J. · Green Chem. · 2010 · 12 · 29610.1039/B919341C ↗
38. Zabeti M. · Fuel Process. Technol. · 2009 · 90 · 77010.1016/j.fuproc.2009.03.010 ↗
39. Chintareddy V. R. · Tetrahedron Lett. · 2011 · 52 · 652310.1016/j.tetlet.2011.09.102 ↗
40. Pramanik M. · Green Chem. · 2012 · 14 · 227310.1039/c2gc35225g ↗
41. Moreno J. I. · Catal. Today · 2011 · 172 · 3410.1016/j.cattod.2011.03.052 ↗
42. Sarkar A. · J. Mol. Catal. A: Chem. · 2010 · 327 · 7310.1016/j.molcata.2010.05.015 ↗