Heterogeneous Catalysis of a Copper-Coated Atomic Force Microscopy Tip for Direct-Write Click Chemistry

Walter F. Paxton, Jason M. Spruell and J. Fraser Stoddart*
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208
J. Am. Chem. Soc., 2009, 131 (19), pp 6692–6694
DOI: 10.1021/ja9015974
Publication Date (Web): April 23, 2009
Copyright © 2009 American Chemical Society

Abstract

Abstract Image

We report a constructive scanning probe lithography method that uses heterogeneous copper-coated atomic force microscopy tips to catalyze azide−alkyne cycloadditions (CuAAC) between solvated terminal alkyne molecules and azide-terminated self-assembled monolayers on silicon surfaces. Spatially controlled surface functionalization was carried out successfully with 50 mM ethanolic solutions of small molecules bearing terminal alkyne groups - propargylamine, 4-pentynoic acid, and an alkynyl-oligoethyleneoxide. We observed that reaction occurs only where the copper tip is in contact with an azide-terminated surface resulting in features with linewidths on the order of 50 nm. The extent of surface functionalization, as measured by changes in surface topography and lateral force microscopy, depends on the scanning force (31−350 nN) and scanning speed, with significant surface patterning observed even at speeds as high as 64 μm/s. In contrast with related SPL techniques, this approach affords a direct-write lithographic approach to constructively modifying and patterning surfaces at the nanoscale without the need for auxiliary reagents. All that is required is (1) an azide surface, (2) a solution of a terminal alkyne, and (3) a copper-coated AFM tip. These advantages allow the direct attachment of a potentially limitless library of molecules that bear terminal alkyne functionalities, including biomolecules, under relatively mild conditions, with sub-100 nm spatial resolution.

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History

  • Published In Issue May 20, 2009
  • Article ASAPApril 23, 2009
  • Received: March 2, 2009

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