Abstract
We report the synthesis of N-isopropylacrylamide-based hydrogels containing either an anionic (acrylic acid) or cationic ([2-(acryloyloxy)ethyl]trimethylammonium chloride) co-monomer. These hydrogels were cross-linked with a cleaveable (N,N′-cystaminebisacrylamide) and/or inert (N,N′-methylenebisacrylamide) molecule in four combinations. Gold nanostructures were then synthesized within these hydrogel matrices by in situ reduction of a metal ion precursor. The resulting eight nanocomposites and their non-gold-containing (native) analogs were characterized with several analytical methods. UV–visible and infrared spectroscopy revealed differences among the samples based largely on the concentration and identity of cross-linking agent. Equilibrium swelling masses and phase transition behavior point to differences among samples on charge of the hydrogel backbone, cross-linker type, and presence or absence of gold nanostructures. A molecular level explanation for these observations is described.
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Acknowledgments
The authors thank Ms. Katherine E. Wagner and Ms. Jessica R. Bell for some methods development with the p(NIPAm-co-ATAC) and p(NIPAm-co-AAc) systems and Ms. Munzarin F. Qayyum for feedback on the manuscript. This work was partially supported by donors of The American Chemical Society Petroleum Research Fund through Grant PRF42899-GB10, by the National Science Foundation (grant CHE-0353813), and by the Department of Chemistry and Brachman Hoffman Program, Wellesley College.
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Guiney, L.M., Agnello, A.D., Thomas, J.C. et al. Thermoresponsive behavior of charged N-isopropylacrylamide-based hydrogels containing gold nanostructures. Colloid Polym Sci 287, 601–608 (2009). https://doi.org/10.1007/s00396-009-2010-7
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DOI: https://doi.org/10.1007/s00396-009-2010-7