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Squish and CuAAC: additive-free covalent monolayers of discrete molecules in seconds
Matthew A Pellow1, T Daniel P Stack, Christopher E D Chidsey
1Department of Chemistry, Stanford University, Stanford, California 94305-5080, United States.
Abstract:
A terminal alkyne is immobilized rapidly into a full monolayer by squishing a small volume of a solution of the alkyne between an azide-modified surface and a copper plate. The monolayer is covalently attached to the surface through a copper-catalyzed alkyne-azide cycloaddition (CuAAC) reaction, and the coverages of the immobilized electroactive alkyne species are quantified by cyclic voltammetry. A reaction time of less than 20 s is possible with no other reagents required. The procedure is effective under aerobic conditions using either an aqueous or aprotic organic solution of the alkyne (1-100 mM).

