Journalartikel
Autorenliste: Garnweitner, G; Smarsly, B; Assink, R; Ruland, W; Bond, E; Brinker, CJ
Jahr der Veröffentlichung: 2003
Seiten: 5626-5627
Zeitschrift: Journal of the American Chemical Society
Bandnummer: 125
Heftnummer: 19
ISSN: 0002-7863
DOI Link: https://doi.org/10.1021/ja0342648
Verlag: American Chemical Society
Abstract:
Thermoresponsive nanocomposite thin films composed of alternating layers of silica and polymerized N-isopropylacrylamide (NIPAM) or NIPAM plus dodecyl methacrylate (DM) hydrogels were prepared by surfactant-directed evaporation-induced self-assembly (EISA). During EISA, the organic monomers partition within the hydrophobic domains of a lamellar mesophase. In-situ polymerization via a free radical process results in a 1-2 nm thick hydrogel phase sandwiched between layers of silica oriented parallel to the substrate surface. The thermoresponsiveness of PNIPAM is preserved in this confined environment, and the polymeric layers reversibly swell and deswell by a factor of 2 in water upon temperature changes around the transition temperature of PNIPAM (32 degrees C). The composition, mesostructure, and environmental response were studied by detailed NMR, TGA, and SAXS analyses.
Zitierstile
Harvard-Zitierstil: Garnweitner, G., Smarsly, B., Assink, R., Ruland, W., Bond, E. and Brinker, C. (2003) Self-assembly of an environmentally responsive polymer/silica nanocomposite, Journal of the American Chemical Society, 125(19), pp. 5626-5627. https://doi.org/10.1021/ja0342648
APA-Zitierstil: Garnweitner, G., Smarsly, B., Assink, R., Ruland, W., Bond, E., & Brinker, C. (2003). Self-assembly of an environmentally responsive polymer/silica nanocomposite. Journal of the American Chemical Society. 125(19), 5626-5627. https://doi.org/10.1021/ja0342648