A self-assembled nanotube for the direct aldol reaction in water

Nanotubes formed by the aqueous assembly of a proline-lysine dipeptide (1) were used to create the hydrophobic microenvironments required to catalyze the aldol reaction in water. The self-assembly process occurred most efficiently in the presence of the substrates, producing an array of homogeneous...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2015-01, Vol.51 (86), p.15653-15656
Hauptverfasser: Lee, Kwang Soo, Parquette, Jon R
Format: Artikel
Sprache:eng
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Zusammenfassung:Nanotubes formed by the aqueous assembly of a proline-lysine dipeptide (1) were used to create the hydrophobic microenvironments required to catalyze the aldol reaction in water. The self-assembly process occurred most efficiently in the presence of the substrates, producing an array of homogeneous nanotubes under the reaction conditions. The nanotubes formed by dipeptide 1 served as an efficient catalyst for the aldol reaction that functioned at low loading levels and provided good to excellent conversions. The catalytic activity of 1 was minimal under conditions that dissociated the nanotube into soluble monomers.
ISSN:1359-7345
1364-548X
DOI:10.1039/c5cc06142c