Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Stephen R. Diegelmann"'
Autor:
Stephen R. Diegelmann, John D. Tovar
Publikováno v:
Macromolecular Rapid Communications. 34:1343-1350
Polydiacetylenes have received intense attention on account of their well-established chromic alterations that are detectable often by the naked eye, making them ideal for a variety of applications such as biosensory materials. These polymers have be
Publikováno v:
Journal of the American Chemical Society. 134:2028-2031
Oligopeptides bearing internal diacetylene units are shown to self-assemble in water into one-dimensional nanostructures and aligned macroscopic hydrogels. The diacetylene units can be photopolymerized into polydiacetylenes that run coincident to the
Autor:
William L. Wilson, Howard E. Katz, Shuming Zhang, John D. Tovar, Stephen R. Diegelmann, Hai-Quan Mao, Thomas J. Dawidczyk, Brian D. Wall
Publikováno v:
Advanced Materials. 23:5009-5014
Autor:
Stephen R. Diegelmann, Kaitlin E. Schrote, Billy Smith, Kevin A. Wepasnick, D. Howard Fairbrother, Hannah K. Wilson
Publikováno v:
Carbon. 49:24-36
Six commonly used wet chemical oxidants (HNO3, KMnO4, H2SO4/HNO3, (NH4)2S2O8, H2O2, and O3) were evaluated in terms of their effects on the surface chemistry and structure of MWCNTs using a combination of analytical techniques. X-ray photoelectron sp
Publikováno v:
Materials
Materials, Vol 3, Iss 2, Pp 1269-1280 (2010)
Materials, Vol 3, Iss 2, Pp 1269-1280 (2010)
This article will highlight our recent work using conjugated oligomers as precursors to electroactive polymer films and self-assembling nanomaterials. One area of investigation has focused on nonbenzenoid aromaticity in the context of charge delocali
Publikováno v:
Chemical communications (Cambridge, England). 46(22)
We report a convenient method to incorporate pi-electron units into peptides that assemble into amyloid-like supramolecular polymers, discussing the scope of the process and preliminary characterization of the resulting nanomaterials. Self-assembly m
Publikováno v:
Journal of the American Chemical Society. 130:13840-13841
The aqueous self-assembly of oligopeptide-flanked pi-conjugated molecules into discrete one-dimensional nanostructures is described. Unique to these molecules is the fact that the pi-conjugated unit has been directly embedded within the peptide backb