The possibility of fabricating self-assembled monolayers (SAMs) from alkylphosphonic acids functionalized with trifluoromethyl derivatives of C-60 on a metal oxide surface has been demonstrated in this work. Using several trifluoromethylfullerenes (TMFs) of different compositions and isomeric structures, we explored their relative reactivities in the Bingel-Hirsch cycloaddition reactions with 11-(diethoxyphosphoryl)undecyl methyl malonate for the first time. Only two isomers of C-60(CF3)(10) showed fairly selective monoadduct formation, whereas compounds with lower CF3 content showed no selectivity. Converting the phosphoric ester into a phosphoric acid moiety enabled the successful formation of self-assembled monolayers of the TMF-alkylphosphonic acid on aluminum oxide surfaces. Comparison with analogous SAMs made with underivatized C-60 showed that TMFs form more hydrophobic surfaces. (C) The Author(s) 2017. Published by ECS.
CITATION STYLE
Clikeman, T. T., Schmaltz, T., Halik, M., Hirsch, A., Strauss, S. H., & Boltalina, O. V. (2017). Formation of Perfluoroalkyl Fullerene Alkylphosphonic Acid Self-Assembled Monolayers on Aluminum Oxide. ECS Journal of Solid State Science and Technology, 6(6), M3163–M3167. https://doi.org/10.1149/2.0281706jss
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