Lehrstuhl für Physikalische Chemie II, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstr. 3, 91058 Erlangen, Germany.
Phys Chem Chem Phys. 2018 Oct 3;20(38):25062-25068. doi: 10.1039/c8cp05255g.
We investigated the metalation and coordination reactions of Co with 2H-5,15-bis(para-cyanophenyl)-10,20-bisphenylporphyrin (2HtransDCNPP) on a Ag(111) surface by scanning tunneling microscopy. At room temperature (RT), 2HtransDCNPPs self-assemble into a supramolecular structure stabilized by intermolecular hydrogen bonding. The metalation of 2HtransDCNPP is achieved either by depositing Co atoms onto the supramolecular structure at RT, or, alternatively, by depositing the molecules onto a submonolayer Co-precovered Ag(111) surface with a subsequent heating to 500 K. In addition, the molecules coordinate to Co atoms through the N atoms in the peripheral cyano groups with a preference of isolated 4-fold coordination motifs at RT.
我们通过扫描隧道显微镜研究了 Co 与 2H-5,15-双(对氰基苯基)-10,20-联苯基卟啉(2HtransDCNPP)在 Ag(111)表面上的金属化和配位反应。在室温下,2HtransDCNPPs 自组装成超分子结构,由分子间氢键稳定。2HtransDCNPP 的金属化可以通过在室温下将 Co 原子沉积到超分子结构上,或者通过将分子沉积到亚单层 Co 预覆盖的 Ag(111)表面上来实现,随后加热至 500 K。此外,分子通过外围氰基基团中的 N 原子与 Co 原子配位,在室温下优先采用孤立的四配位模式。