Poly-l-Lysine Templated Silicas: Using Polypeptide Secondary Structure to Control Oxide Pore Architectures
Abstract
Utilizing polypeptide secondary structure as a means for controlling oxide pore architectures is explored. Poly-l-lysine is used as a model polypeptide as its folding behavior is well understood and compatible with the sol−gel chemistry of silica. Here, we show that silicas synthesized with poly-l-lysine in a α-helix conformation possess cylindrical pores that are approximately 1.5 nm in size, whereas silicas synthesized with poly-l-lysine in a β-sheet conformation possess larger pores, the size of which are a function of the poly-l-lysine concentration, or in other words the size of the aggregate. In both cases, highly porous materials are obtained. In-situ circular dichroism measurements of the synthesis mixtures show that the poly-l-lysine secondary structure is not perturbed during synthesis. Infrared spectroscopy of the as-synthesized materials is consistent with the poly-l-lysine retaining its secondary structure. Grand canonical Monte Carlo simulations were also performed to validate the interpretation of the experimental adsorption results. The experimental isotherms are consistent with simulated isotherms of cylindrical pores 1.3−1.7 nm in size, in good agreement with expected values. Our results suggest a new avenue for synthesizing porous oxides with highly tuneable pore sizes and shapes under mild conditions.
Additional Information
© 2004 American Chemical Society. Received 5 January 2004. Published online 2 July 2004. Published in print 1 July 2004. K.M.H. acknowledges the Engineering Academic Programs Office at Texas A&M for a summer research fellowship. K. M. H. and D. F. S. also acknowledge the Texas Advanced Research Program for financial support. The SAXS instrument was purchased from funds obtained under NSF grant CTS-0215838. The authors acknowledge the Microscopy and Imaging Center (MIC) at Texas A&M for access to the FE-SEM and TEM instrumentation. The authors also thank T. Good and J. M. Scholtz for useful discussions, J. Schmittschmitt for discussions about the CD experiments, H. Cheng for acquiring SAXS data on the PLL solutions, and Texas A&M University for financial support.Attached Files
Supplemental Material - ja049936osi20040521_114208.pdf
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Additional details
- Eprint ID
- 76793
- Resolver ID
- CaltechAUTHORS:20170421-074322738
- Texas A&M University
- Texas Advanced Research Program
- CTS-0215838
- NSF
- Created
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2017-04-21Created from EPrint's datestamp field
- Updated
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2021-11-15Created from EPrint's last_modified field