Acid properties of organosiliceous hybrid materials based on pendant (fluoro)aryl-sulfonic groups through a spectroscopic study with probe molecules. Issue 22 (17th October 2019)
- Record Type:
- Journal Article
- Title:
- Acid properties of organosiliceous hybrid materials based on pendant (fluoro)aryl-sulfonic groups through a spectroscopic study with probe molecules. Issue 22 (17th October 2019)
- Main Title:
- Acid properties of organosiliceous hybrid materials based on pendant (fluoro)aryl-sulfonic groups through a spectroscopic study with probe molecules
- Authors:
- Erigoni, Andrea
Paul, Geo
Meazza, Marta
Hernández-Soto, María Consuelo
Miletto, Ivana
Rios, Ramon
Segarra, Candela
Marchese, Leonardo
Raja, Robert
Rey, Fernando
Gianotti, Enrica
Díaz, Urbano - Abstract:
- Abstract : Hybrid heterogeneous catalysts containing (fluoro)aryl-sulfonic groups were characterized through combined spectroscopic techniques and adsorption of probe molecules, with their reactivity being modulated for acetal formation. Abstract : Two different heterogeneous catalysts carrying aryl-sulfonic moieties, in which the aromatic ring was either fluorinated or not, were successfully synthesized. The multi-step synthetic approaches implemented involved the synthesis of the silyl-derivative, template-free one-pot co-condensation (at low temperature and neutral pH) and tethering reaction. A multi-technique approach was implemented to characterize the hybrid organic–inorganic catalysts involving TGA, N2 physisorption analysis, FTIR spectroscopy, and ss MAS NMR ( 1 H, 13 C, 29 Si) spectroscopy. Specifically, the acidity of the organosiliceous hybrid materials was studied through the adsorption of probe molecules ( i.e. CO at 77 K and NH3 and TMPO at room temperature) and a combination of FTIR and ss MAS NMR spectroscopy. The catalytic activity of the two hybrids was tested in the acetal formation reaction between benzaldehyde and ethylene glycol. Preliminary results indicated superior performances for the fluoro-aryl-sulfonic acid, compared to the non-fluorinated sample. The findings hereby reported open new avenues for the design of heterogeneous sulfonic acids with superior reactivity in acid-catalyzed reactions. Moreover, through the implementation of spectroscopicAbstract : Hybrid heterogeneous catalysts containing (fluoro)aryl-sulfonic groups were characterized through combined spectroscopic techniques and adsorption of probe molecules, with their reactivity being modulated for acetal formation. Abstract : Two different heterogeneous catalysts carrying aryl-sulfonic moieties, in which the aromatic ring was either fluorinated or not, were successfully synthesized. The multi-step synthetic approaches implemented involved the synthesis of the silyl-derivative, template-free one-pot co-condensation (at low temperature and neutral pH) and tethering reaction. A multi-technique approach was implemented to characterize the hybrid organic–inorganic catalysts involving TGA, N2 physisorption analysis, FTIR spectroscopy, and ss MAS NMR ( 1 H, 13 C, 29 Si) spectroscopy. Specifically, the acidity of the organosiliceous hybrid materials was studied through the adsorption of probe molecules ( i.e. CO at 77 K and NH3 and TMPO at room temperature) and a combination of FTIR and ss MAS NMR spectroscopy. The catalytic activity of the two hybrids was tested in the acetal formation reaction between benzaldehyde and ethylene glycol. Preliminary results indicated superior performances for the fluoro-aryl-sulfonic acid, compared to the non-fluorinated sample. The findings hereby reported open new avenues for the design of heterogeneous sulfonic acids with superior reactivity in acid-catalyzed reactions. Moreover, through the implementation of spectroscopic studies, using probe molecules, it was possible to investigate in detail the acidic properties of hybrid organosiliceous materials. … (more)
- Is Part Of:
- Catalysis science & technology. Volume 9:Issue 22(2019)
- Journal:
- Catalysis science & technology
- Issue:
- Volume 9:Issue 22(2019)
- Issue Display:
- Volume 9, Issue 22 (2019)
- Year:
- 2019
- Volume:
- 9
- Issue:
- 22
- Issue Sort Value:
- 2019-0009-0022-0000
- Page Start:
- 6308
- Page End:
- 6317
- Publication Date:
- 2019-10-17
- Subjects:
- Catalysis -- Periodicals
541.395 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/CY ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9cy01609k ↗
- Languages:
- English
- ISSNs:
- 2044-4753
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3090.943100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12099.xml