0000000000207836
AUTHOR
Frank Auer
Odd-even chain length-dependent order in pH-switchable self-assembled layers.
The reversible self-assembly of a series of bipolar amphiphiles, alpha,omega-bis(3- or 4-amidinophenoxy)alkanes (chain length n = 5-12), on mercaptoalkanoic acid-functionalized gold surfaces (chain length n = 10, 11, 14, 15) has been studied by in-situ ellipsometry, IR reflection absorption spectroscopy (IRAS), and atomic force microscopy (AFM). The layer order, amphiphile orientation, and tendency to form bilayers depends on the position of the amidine substituent, the alkyl chain length of both the amidine amphiphile and the underlying acid self-assembled monolayer (SAM), and whether the amidine alkyl chain contained an even or odd number of methylene groups. Thus, para-substituted bisben…
Switchable assembly of stable, ordered molecular layers
Bisamidines can be assembled on self-assembled monolayers of mercaptoalkanoic acids on gold to form stable and ordered but pH-switchable layers (see diagram). At basic pH the layers are stable and charge selective towards charged surfactants and plasma proteins. The system can potentially be used to reversibly introduce new surface properties for given applications that use one single substrate.
Nanocomposites by Electrostatic Interactions: 1. Impact of Sublayer Quality on the Organization of Functionalized Nanoparticles on Charged Self-Assembled Layers
Bis-benzamidines were studied as linkers for the formation of gold nanoparticle assemblies on planar gold surfaces modified with ω-mercaptohexadecanoic acid. In situ ellipsometry, external reflecti...