Folkertsma Emma, van der Lit Joost, Di Cicco Francesca, Lutz Martin, Klein Gebbink Robertus J M, Swart Ingmar, Moret Marc-Etienne
Organic Chemistry & Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.
Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science, Utrecht University, P.O. Box 80000, 3508 TA Utrecht, The Netherlands.
ACS Omega. 2017 Apr 30;2(4):1372-1379. doi: 10.1021/acsomega.6b00510. Epub 2017 Apr 10.
Here, we report the bulk synthesis of [Fe(BMBIK)Cl] bearing the redox noninnocent bis(methylbenzimidazolyl)ketone (BMBIK) ligand and the synthesis of the similar complex [Fe(BMBIK)] on a Au(111) surface using lateral manipulation at the atomic level. Cyclic voltammetry and scanning tunneling spectroscopy are shown to be useful techniques to compare the coordination compound in solution with the one on the surface. The total charge, as well as the oxidation and spin state of [Fe(BMBIK)], are investigated by comparison of the shape of the lowest unoccupied molecular orbital (LUMO), visualized by tunneling through the LUMO, with theoretical models. The similar reduction potentials found for the solution and surface compounds indicate that the major effect of lowering the LUMO upon coordination of BMBIK to the iron center is conserved on the surface. The synthesis and analysis of [Fe(BMBIK)] using scanning tunneling microscopy, scanning tunneling spectroscopy, and atomic force microscopy are the first steps toward mechanistic studies of homogeneous catalysts with redox noninnocent ligands at the single molecule level.
在此,我们报告了带有氧化还原非惰性双(甲基苯并咪唑基)酮(BMBIK)配体的[Fe(BMBIK)Cl]的批量合成,以及在Au(111)表面通过原子水平的横向操纵合成类似配合物[Fe(BMBIK)]。循环伏安法和扫描隧道光谱法被证明是比较溶液中的配位化合物与表面上的配位化合物的有用技术。通过将通过最低未占据分子轨道(LUMO)隧穿可视化的LUMO形状与理论模型进行比较,研究了[Fe(BMBIK)]的总电荷以及氧化态和自旋态。溶液和表面化合物发现的类似还原电位表明,BMBIK与铁中心配位时降低LUMO的主要作用在表面上得以保留。使用扫描隧道显微镜、扫描隧道光谱法和原子力显微镜对[Fe(BMBIK)]进行合成和分析,是在单分子水平上对具有氧化还原非惰性配体的均相催化剂进行机理研究的第一步。