Haensch Claudia, Chiper Manuela, Ulbricht Christoph, Winter Andreas, Hoeppener Stephanie, Schubert Ulrich S
Laboratory of Macromolecular Chemistry and Nanoscience, Eindhoven University of Technology, Eindhoven, The Netherlands.
Langmuir. 2008 Nov 18;24(22):12981-5. doi: 10.1021/la8026682. Epub 2008 Oct 17.
We report on the reversible and selective functionalization of surfaces by utilizing supramolecular building blocks. The reversible formation of terpyridine bis-complexes, based on a terpyridine ligand-functionalized monolayer, is used as a versatile supramolecular binding motif. Thereby, click chemistry was applied to covalently bind an acetylene functionalized Fe(II) bis-complex onto azide-terminated self-assembled monolayers. By decomplexation of the formed supramolecular complex, the ligand modified monolayer could be obtained. These monolayers were subsequently used for additional complexation reactions, resulting in the reversible functionalization of the substrates. The proper choice of the coordinating transition metal ions allows the tuning of the binding strength, as well as the physicochemical properties of the formed complexes and thus an engineering of the surface properties.
我们报道了利用超分子构建块对表面进行可逆和选择性功能化。基于三联吡啶配体功能化单分子层的三联吡啶双配合物的可逆形成,被用作通用的超分子结合基序。由此,应用点击化学将乙炔功能化的Fe(II)双配合物共价结合到叠氮基封端的自组装单分子层上。通过形成的超分子配合物的解络合,可以得到配体修饰的单分子层。这些单分子层随后用于额外的络合反应,从而实现底物的可逆功能化。配位过渡金属离子的适当选择能够调节结合强度以及所形成配合物的物理化学性质,进而对表面性质进行工程设计。