The construction of a donor–acceptor
Stenhouse adduct molecular
layer on a gold surface is presented. To avoid the incompatibility
of the thiol surface-binding group with the donor–acceptor
polyene structure of the switch, an interfacial reaction approach
was followed. Poly(dopamine)-supported gold nanoparticles on quartz
slides were chosen as substrates, which was expected to facilitate
both the interfacial reaction and the switching process by providing
favorable steric conditions due to the curved particle surface. The
reaction between the surface-bound donor half and the CF
3
-isoxazolone-based acceptor half was proved to be successful by X-ray
photoelectron spectroscopy (XPS). However, UV–vis measurements
suggested that a closed, cyclopentenone-containing structure of the
switch formed on the surface irreversibly. Analysis of the wetting
behavior of the surface revealed spontaneous water spreading that
could be associated with conformational changes of the closed isomer.