Abstract
Herein we describe the design and synthesis of a redox-dependent single-molecule switch. Appending a ferrocene unit to a diphenylacetylene scaffold gives a redox-sensitive handle, which undergoes reversible one-electron oxidation, as demonstrated by cyclic voltammetry analysis. 1H-NMR spectroscopy of the partially oxidized switch and control compounds suggests that oxidation to the ferrocenium cation induces a change in hydrogen bonding interactions that results in a conformational switch. © 2014 by the authors.
Author supplied keywords
Cite
CITATION STYLE
Jones, I. M., Knipe, P. C., Michaelos, T., Thompson, S., & Hamilton, A. D. (2014). Redox-dependent conformational switching of diphenylacetylenes. Molecules, 19(8), 11316–11332. https://doi.org/10.3390/molecules190811316
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.