Department of Physics, The Hong Kong University of Science and Technology , Clear Water Bay, Hong Kong.
ACS Nano. 2014 Aug 26;8(8):8310-6. doi: 10.1021/nn502765g. Epub 2014 Aug 8.
We present an investigation of two-dimensional coordination networks formed by 5,10,15,20-tetra(4-pyridyl)porphyrin and iron atoms on a Au(111) surface. The coordination bonds are very robust as evidenced by STM manipulated lateral displacement of an entire network of islands consisting of hundreds of molecules and atoms. We also applied vertical manipulation to detach and attach single Fe atoms at the coordination sites. Moreover, low-temperature tunneling spectroscopy reveals a Kondo resonance at the Fe coordination center. These findings evidence that the network structure is stabilized by a coordination motif in which a pair of vertically aligned Fe atoms is ligated by four equatorial pyridyl groups. Such out-of-plane dinuclear coordination centers provide potential functions, such as catalytic, adsorption, and template for growing three-dimensional framework architectures.
我们研究了由 5,10,15,20-四(4-吡啶基)卟啉和铁原子在 Au(111)表面形成的二维配位网络。STM 操纵整个由数百个分子和原子组成的岛屿网络的横向位移证明了配位键非常稳定。我们还应用垂直操纵来在配位位置上分离和连接单个 Fe 原子。此外,低温隧道谱揭示了配位中心的 Kondo 共振。这些发现证明了网络结构是由配位模式稳定的,其中一对垂直排列的 Fe 原子通过四个赤道吡啶基团连接。这种面外双核配位中心提供了潜在的功能,例如催化、吸附和模板,用于生长三维框架结构。