10.1021/la0362977.s001
James P. Collman
James P.
Collman
Neal K. Devaraj
Neal K.
Devaraj
Christopher E. D. Chidsey
Christopher
E. D. Chidsey
“Clicking” Functionality onto Electrode Surfaces
American Chemical Society
2004
Electrode Surfaces
electrode surface
metal surfaces
reaction proceeds
triazole group
Ferrocene immobilization
monolayer
room temperature
functionalizing surfaces
2004-02-17 00:00:00
Journal contribution
https://acs.figshare.com/articles/journal_contribution/_Clicking_Functionality_onto_Electrode_Surfaces/3349936
We demonstrate the applicability of Sharpless “click” chemistry, specifically Huisgen 1,3-dipolar
cycloadditions, as a general methodology for functionalizing surfaces coated with self-assembled monolayers.
Ferrocene immobilization was used as our model, and the resulting monolayers were analyzed using
traditional surface analytical techniques. Our preliminary results indicate that this reaction proceeds to
completion at room temperature in aqueous solvent. The triazole group is a thermally and hydrolytically
stable, conjugated linkage. The reactants, acetylenes and azides, are independently stable; they do not
react with common organic reagents or with themselves. Thus the potential for this reaction to immobilize
a wide range of functionally complex substances on metal surfaces is significant. To our knowledge this
is the first report of the use of “click” chemistry to modify a well-defined electrode surface.