journal article·2014-06-25Open access

Improved Catalytic Activity and Stability Using Mixed Sulfonic Acid- and Hydroxy-Bearing Polymer Brushes in Microreactors

Roberto Ricciardi, Rajesh Munirathinam, Jurriaan Huskens, Willem Verboom

Abstract

Sulfonic acid-bearing polymer brushes were grown on the inner walls of continuous flow glass microreactors and used in the acid-catalyzed hydrolysis of benzaldehyde dimethyl acetal as a test reaction. Randomly 1:1 mixed polymer brushes of poly-3-sulfopropyl methacrylate (PSPM) and poly-2-hydroxyethyl methacrylate (PHEMA) showed a 6-fold increase of the TOF value compared to the solely PSPM-containing microreactor. This remarkable improvement is attributed to the cooperative stabilizing effect of proximal OH groups on the active sulfonic acid moieties within the brush architecture. In fact, the rational mixing of SPM with methyl methacrylate (MMA) as an OH-free comonomer caused a drop in the activity of the resulting catalytic platform. A 5-fold increase of the TON of the 1:1 PSPM-PHEMA versus the PSPM homopolymer brush systems additionally demonstrates the substantial increase in the stability of the mixed brushes catalytic platform, which could be continuously run over 7 days without significant loss of activity. The 1:1 PSPM-PHEMA mixed brush catalytic system also showed a good activity in the deprotection of 2-benzyl tetrahydropyranyl ether.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Innovative Microfluidic and Catalytic Techniques Innovation · Microfluidic and Capillary Electrophoresis Applications · 3D Printing in Biomedical Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Laboratory of Molecular Nanofabrication, MESA+ Institute for Nanotechnology, University of Twente, P.O. Box 217, 7500 AE Enschede, The Netherlands

References (48)

Show source-provided references
1. Frost C. G. · Green Chem. · 2010 · 12 · 168710.1039/c0gc00133c ↗
2. Elvira K. S. · Nat. Chem. · 2013 · 5 · 90510.1038/nchem.1753 ↗
3. Whitesides G. M. · Nature · 2006 · 442 · 36810.1038/nature05058 ↗
4. Wiles C. · Chem. Commun. · 2011 · 47 · 651210.1039/c1cc00089f ↗
5. Brivio M. · Lab Chip · 2006 · 6 · 32910.1039/b510856j ↗
6. Hartman R. L. · Lab Chip · 2009 · 9 · 249510.1039/b906343a ↗
7. Wiles C. · Green Chem. · 2012 · 14 · 3810.1039/C1GC16022B ↗
8. Poliakoff M. · Science · 2002 · 297 · 80710.1126/science.297.5582.807 ↗
9. Mason B. P. · Chem. Rev. · 2007 · 107 · 230010.1021/cr050944c ↗
10. Xu B.-B. · ChemCatChem. · 2013 · 5 · 209110.1002/cctc.201200863 ↗
11. Wiles C. · ChemSusChem · 2012 · 5 · 33210.1002/cssc.201100370 ↗
12. de M. Muñoz J. · Adv. Synth. Catal. · 2012 · 354 · 345610.1002/adsc.201200678 ↗
13. Deverell J. A. · Sens. Actuators B · 2011 · 155 · 38810.1016/j.snb.2010.11.020 ↗
14. Lange P. P. · Chem. Commun. · 2011 · 47 · 362810.1039/c0cc05708h ↗
15. Klemm E. · Chem. Eng. Technol. · 2007 · 30 · 161510.1002/ceat.200700311 ↗
16. Stojkovič G. · Microfluid. Nanofluid. · 2011 · 10 · 62710.1007/s10404-010-0696-y ↗
17. Costantini F. · J. Am. Chem. Soc. · 2009 · 131 · 165010.1021/ja807616z ↗
18. Ftouni J. · Chem. Eng. J. · 2013 · 227 · 10310.1016/j.cej.2012.08.071 ↗
19. Orski S. V. · J. Mater. Chem. · 2011 · 21 · 1413510.1039/c1jm11039j ↗
20. Brittain W. J. · J. Polym. Sci., Part A: Polym. Chem. · 2007 · 45 · 350510.1002/pola.22180 ↗
21. Zeltner M. · J. Mater. Chem. · 2011 · 21 · 299110.1039/c0jm03338c ↗
22. Gill C. · Catal. Lett. · 2009 · 131 · 42510.1007/s10562-009-0099-4 ↗
23. Zhao B. · J. Polym. Sci., Part A: Polym. Chem. · 2008 · 46 · 343810.1002/pola.22681 ↗
24. Huang J. · Macromol. Biosci. · 2008 · 8 · 50810.1002/mabi.200700256 ↗
25. Costantini F. · Chem.—Eur. J. · 2010 · 16 · 1240610.1002/chem.201000948 ↗
26. Costantini F. · Lab Chip · 2010 · 10 · 340710.1039/c0lc00187b ↗
27. Munirathinam R. · Beilstein J. Org. Chem. · 2013 · 9 · 169810.3762/bjoc.9.194 ↗
28. Fernandes A. E. · Chem. – Eur. J. · 2012 · 18 · 1622610.1002/chem.201202531 ↗
29. Corma A. · Adv. Synth. Catal. · 2006 · 348 · 139110.1002/adsc.200606192 ↗
30. Harmer M. A. · Appl. Catal. A · 2001 · 221 · 4510.1016/S0926-860X(01)00794-3 ↗
31. Melero J. A. · Chem. Rev. · 2006 · 106 · 379010.1021/cr050994h ↗
32. Wang W. · J. Mater. Chem. · 2012 · 22 · 1587410.1039/c2jm32894a ↗
33. El Kadib A. · Chem. Commun. · 2013 · 49 · 907310.1039/c3cc45160g ↗
34. Nakajima K. · ACS Catal. · 2012 · 2 · 129610.1021/cs300103k ↗
35. Long W. · ACS Catal. · 2011 · 1 · 67410.1021/cs2001175 ↗
36. Liu F. · ACS Catal. · 2012 · 2 · 56510.1021/cs200613p ↗
37. Tian C. · Chem. Commun. · 2013 · 49 · 866810.1039/c3cc43127d ↗
38. Wiles C. · Lab Chip · 2007 · 7 · 32210.1039/B615069A ↗
39. El Kadib A. · Angew. Chem., Int. Ed. · 2009 · 48 · 496910.1002/anie.200805580 ↗
40. Ricciardi R. · J. Flow Chem. · 2013 · 3 · 12710.1556/JFC-D-13-00024 ↗
41. Husseman M. · Macromolecules · 1999 · 32 · 142410.1021/ma981290v ↗
42. Ramstedt M. · Langmuir · 2007 · 23 · 331410.1021/la062670+ ↗
43. Altıokka M. R. · Ind. Eng. Chem. Res. · 2007 · 46 · 105810.1021/ie060716o ↗
44. Gill C. S. · Chem.—Eur. J. · 2008 · 14 · 730610.1002/chem.200800532 ↗
45. Shokri A. · J. Am. Chem. Soc. · 2013 · 135 · 1791910.1021/ja408762r ↗
46. Guthrie J. P. · J. Am. Chem. Soc. · 1993 · 115 · 1156910.1021/ja00077a063 ↗
47. Stephens J. R. · Eur. J. Org. Chem. · 2003 · 382710.1002/ejoc.200300295 ↗
48. Bandgar B. P. · Monatsh. Chem. · 2003 · 134 · 42510.1007/s00706-002-0468-9 ↗