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. Author manuscript; available in PMC: 2012 Jan 12.
Published in final edited form as: Chemistry. 2011 Jan 24;17(9):2656–2665. doi: 10.1002/chem.201001533

Scheme 1.

Scheme 1

Surface hydrosilylation using a mixture of the TMG-protected alkenyne TMG-EG10 and the alkene EG7 on H-terminated Si(111) surfaces, followed by attachment of IG-25 with an azido tag (N3-IG-25). The mole fraction of TMG-EG10 was 1.0, 0.4, 0.2, 0.1, 0.05 or 0, to afford the corresponding surface 1a–f, respectively. The corresponding peptide-presenting surfaces 2ae are formed upon CuAAC reaction of N3-IG-25 with the TMG-alkyne surfaces 1ae.