Gold nanoparticles are separated
above a planar gold film by 1.1 nm thick self-assembled molecular
monolayers of different conductivities. Incremental replacement of
the nonconductive molecules with a chemically equivalent conductive
version differing by only one atom produces a strong 50 nm blue-shift
of the coupled plasmon. With modeling this gives a conductance of
0.17G0 per biphenyl-4,4′-dithiol
molecule and a total conductance across the plasmonic junction of
30G0. Our approach provides a reliable
tool quantifying the number of molecules in each plasmonic hotspot,
here <200.
Drop-casting [Fe(bpp)2][BF4]2 (bpp = 2,6-di[pyrazol-1-yl]pyridine) onto HOPG affords chain-of-beads nanostructures. SAMs of bpp derivatives with sulfur-containing tethers are also described.
We present an efficient solid phase synthesis methodology that provides easy access to a range of functionalised long-chain alkanethiol-oligoethyleneglycols that form well-defined self-assembled monolayers on gold and are compatible with pre- or post-assembly conjugation of (bio)molecules. We demonstrate the versatility of our synthetic route by synthesising LCAT-OEGs with a range of functional moieties, including peptides, electro-active redox groups, chemical handles for post-assembly conjugation of (bio)molecules, and demonstrate the application of our LCAT-OEG monolayers in immunosensing, where they show good biocompatibility with minimal biofouling.
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