| Literature DB >> 15984878 |
Alfonso Ortiz-Acevedo1, Hui Xie, Vasiliki Zorbas, William M Sampson, Alan B Dalton, Ray H Baughman, Rockford K Draper, Inga H Musselman, Gregg R Dieckmann.
Abstract
We have utilized reversible cyclic peptides (RCPs)-peptides containing alternating l- and d-amino acids with N- and C-termini derivatized with thiol-containing groups allowing reversible peptide cyclization-to solubilize and noncovalently functionalize carbon single-walled nanotubes (SWNTs) in aqueous solution. Solubilization occurs through wrapping of RCPs around the circumference of a SWNT, followed by the formation of head-to-tail covalent bonds, yielding closed rings on the nanotubes. By controlling the length of the RCPs, we have demonstrated limited diameter-selective solubilization of the SWNTs as revealed by UV/vis/NIR and Raman spectroscopies, as well as atomic force microscopy.Entities:
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Year: 2005 PMID: 15984878 DOI: 10.1021/ja050507f
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419