Spatially controlled Suzuki and Heck catalytic molecular coupling

The initiation and control of chemical coupling has the potential to offer much within the context of bottom up nanofabrication. We report herein the use of a palladium-modified, catalytically active, AFM probe to initiate and spatially control surface-confined Suzuki and Heck carbon-carbon coupling reactions. These chemically written reactions, detectable by lateral force and chemically specific optical and topographic labeling, were patterned with line widths down to 15 nm or similar to 20 molecules. Catalyzed organometallic coupling was, in this way, carried out at subzeptomolar levels. By varying the catalyst-substrate interaction times, turnover numbers of (0.6-1.2) x 10(4) and (3.0-5.0) x 10(4) molecules s(-1) were resolved for Suzuki and Heck reactions, respectively.