journal article·2012-05-22

Covalent Layer-by-Layer Assembly of Water-Permeable and Water-Impermeable Polymer Multilayers on Highly Water-Soluble and Water-Sensitive Substrates

Adam H. Broderick, Uttam Manna, David M. Lynn

Chemistry of Materials· Volume 24· Issue 10
Publisher page

Abstract

Aqueous methods for the layer-by-layer (LbL) assembly of polyelectrolyte multilayers (PEMs) are not, by their nature, well suited for the fabrication of thin films on substrates that are highly water-soluble or composed of water-sensitive materials. Here, we demonstrate that organic solvent-based processes for covalent (or “reactive”) LbL assembly can be used to fabricate multilayers directly on the surfaces of model water-soluble, water-reactive, and water-sensitive substrates that are either difficult or impossible to coat effectively using aqueous-based LbL methods. Our approach is based on methods for the reactive assembly of multilayers using poly(ethyleneimine) (PEI) and an amine-reactive polymer containing azlactone functionality (PVMDA) in polar-aprotic solvents. The amine-reactive nature of the resulting PEI/PVDMA films facilitated subsequent modification of film-coated surfaces by reaction with primary amine-based nucleophiles. Functionalization of films with the hydrophobic small-molecule amine n -decylamine resulted in the prolonged dissolution and release of underlying water-soluble substrates, and could be used to tune interfacial properties (e.g., to render these water-permeable films more hydrophobic). Fabrication of thicker PEI/PVDMA films resulted in coatings with superhydrophobic properties (e.g., water contact angles of ∼160°) that resisted the penetration of water and enhanced considerably the stabilities of water-sensitive substrates. This approach can, therefore, also be used, in various ways, and to varying extents, to design barriers that protect, enhance the stabilities of, or control/pattern the responses of water-soluble/reactive substrates when they are exposed to aqueous environments. Finally, our results demonstrate that the solubility of PEI and PVDMA in a range of different polar-aprotic solvents can provide flexibility with respect to coating water-soluble/sensitive materials that may also be soluble in some other polar organic solvents. The versatility of this approach could prove useful for modifying the interfacial properties of water-soluble and water-sensitive materials of interest in biotechnology, catalysis, and many other fundamental and applied contexts.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Polymer Surface Interaction Studies · Molecular Junctions and Nanostructures · Surface Modification and Superhydrophobicity

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

Affiliations

Department of Chemical and Biological Engineering, 1415 Engineering Drive, University of Wisconsin-Madison, Madison, Wisconsin 53706

References (50)

Show source-provided references
1. Decher G. · Science · 1997 · 277 · 123210.1126/science.277.5330.1232 ↗
2. Bertrand P. · Macromol. Rapid Commun. · 2000 · 21 · 31910.1002/(SICI)1521-3927(20000401)21:7<319::AID-MARC319>3.0.CO;2-7 ↗
3. Schonhoff M. · Curr. Opin. Colloid Interface Sci. · 2003 · 8 · 8610.1016/S1359-0294(03)00003-7 ↗
4. Decher G. · 2003
5. Ai H. · Cell Biochem. Biophys. · 2003 · 39 · 2310.1385/CBB:39:1:23 ↗
6. Hammond P. T. · Adv. Mater. · 2004 · 16 · 127110.1002/adma.200400760 ↗
7. Sukhishvili S. A. · Curr. Opin. Colloid Interface Sci. · 2005 · 10 · 3710.1016/j.cocis.2005.05.001 ↗
8. Tang Z. Y. · Adv. Mater. · 2006 · 18 · 320310.1002/adma.200600113 ↗
9. De Geest B. G. · Soft Matter · 2009 · 5 · 28210.1039/B808262F ↗
10. Boudou T. · Adv. Mater. · 2010 · 22 · 44110.1002/adma.200901327 ↗
11. Jewell C. M. · Adv. Drug Delivery Rev. · 2008 · 60 · 97910.1016/j.addr.2008.02.010 ↗
12. Tuo X. L. · Acta Polym. Sin. · 2006 · 15610.3724/SP.J.1105.2006.00156 ↗
13. Beyer S. · Langmuir · 2007 · 23 · 882710.1021/la7011777 ↗
14. Kamineni V. K. · Langmuir · 2007 · 23 · 742310.1021/la700465n ↗
15. Bai J. · Soft Matter · 2009 · 5 · 415210.1039/b909305b ↗
16. Mak W. C. · Langmuir · 2009 · 25 · 76910.1021/la8029962 ↗
17. Lin L. Y. · Angew Chem., Int. Ed. · 2010 · 49 · 977310.1002/anie.200907321 ↗
18. Borodina T. N. · ACS Appl. Mater. Interfaces · 2009 · 1 · 99610.1021/am8002236 ↗
19. Buck M. E. · Adv. Mater. · 2007 · 19 · 395110.1002/adma.200700822 ↗
20. Buck M. E. · Biomacromolecules · 2009 · 10 · 156410.1021/bm9001552 ↗
21. Buck M. E. · ACS Appl. Mater. Interfaces · 2010 · 2 · 142110.1021/am1000882 ↗
22. Buck M. E. · Chem. Mater. · 2010 · 22 · 631910.1021/cm102115e ↗
23. Broderick A. H. · Biomacromolecules · 2011 · 12 · 199810.1021/bm200296a ↗
24. Buck M. E. · Polym. Chem. · 2012 · 3 · 6610.1039/C1PY00314C ↗
25. Quinn J. F. · Chem. Soc. Rev. · 2007 · 36 · 70710.1039/b610778h ↗
26. Bergbreiter D. E. · Soft Matter · 2009 · 5 · 2310.1039/B810852H ↗
27. Serizawa T. · Macromolecules · 2002 · 35 · 218410.1021/ma011465s ↗
28. Tian Y. · Langmuir · 2006 · 22 · 36010.1021/la0524768 ↗
29. Feng Z. · Adv. Mater. · 2007 · 19 · 368710.1002/adma.200700541 ↗
30. Liu Y. · J. Am. Chem. Soc. · 1997 · 119 · 872010.1021/ja972075h ↗
31. Russell R. J. · Langmuir · 2000 · 16 · 405210.1021/la991388i ↗
32. Major J. S. · Chem. Mater. · 2002 · 14 · 257410.1021/cm011644o ↗
33. Zhang Y. · Macromolecules · 2003 · 36 · 423810.1021/ma0342729 ↗
34. Such G. K. · J. Am. Chem. Soc. · 2006 · 128 · 931810.1021/ja063043+ ↗
35. Bergbreiter D. E. · Macromolecules · 2007 · 40 · 533710.1021/ma0701134 ↗
36. Vestberg R. · J. Polym. Sci., Part A: Polym. Chem · 2007 · 45 · 283510.1002/pola.22178 ↗
37. Park H. J. · Langmuir · 2008 · 24 · 1046710.1021/la801341t ↗
38. Gill R. · Angew. Chem., Int. Ed. Engl. · 2010 · 49 · 611610.1002/anie.200907161 ↗
39. Seo J. · Langmuir · 2010 · 26 · 183010.1021/la902574z ↗
40. El Haitami A. E. · Langmuir · 2010 · 26 · 1235110.1021/la101670g ↗
41. Manna U. · Chem. Commun. · 2010 · 46 · 225010.1039/b924240f ↗
42. Huang C.-J. · Macromolecules · 2009 · 42 · 515510.1021/ma900478n ↗
43. Buck M. E. · Adv. Mater. · 2010 · 22 · 99410.1002/adma.200903054 ↗
44. Rard J. A. · J. Chem. Eng. Data · 1997 · 42 · 81910.1021/je9700582 ↗
45. Buck M. E. · Langmuir · 2010 · 26 · 1613410.1021/la103009a ↗
46. Tocce E. J. · J. Biomed. Mater. Res., Part A · 2012 · 100 · 8410.1002/jbm.a.33233 ↗
47. Beecken H. · Biotechnol. Histochem. · 2003 · 78 · 28910.1080/10520290410001671362 ↗
48. Roach P. · Soft Matter · 2008 · 4 · 22410.1039/B712575P ↗
49. Zhang X. · J. Mater. Chem. · 2008 · 18 · 62110.1039/B711226B ↗
50. Katzin L. I. · J. Am. Chem. Soc. · 1952 · 74 · 275210.1021/ja01131a016 ↗