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O: Fachverband Oberflächenphysik
O 64: Metal Substrates: Adsorption of Organic/Bio Molecules IV
O 64.4: Vortrag
Donnerstag, 28. Februar 2008, 12:00–12:15, HE 101
Formation, electronic structure, and reactivity of adsorbed metalloporphyrin complexes — •J. Michael Gottfried, Ken Flechtner, Yun Bai, Andreas Kretschmann, Marie-Madeleine Walz, Andreas Bayer, and Hans-Peter Steinrück — Universität Erlangen-Nürnberg, Lehrstuhl für Physikalische Chemie II
Supported metal complexes are promising candidates for novel, regularly nanostructured catalysts. The coordinated metal centers represent well-defined active sites, which are immobilized by anchoring the ligands to a solid surface. Thus, these systems combine the advantages of homogeneous and heterogeneous catalysts. To develop a fundamental understanding of their functional principles, we have studied the formation, the electronic structure, and the reactivity of various porphyrin-based metal complexes on Ag(111) using photoelectron spectroscopy and complementary techniques. Specifically, we will discuss the axial coordination of NO on adsorbed Co(II)-tetraphenylporphyrin (CoTPP) and the influence of this ligand on the electronic interaction between the Co ion and the underlying Ag surface.1 In addition, the formation of the complex H3N-ZnTPP (by reaction between tetraphenylporphyrin, Zn, and NH3 on an Ag(111) surface) will be used to illustrate a novel two-step route for the in-situ synthesis of adsorbed metalloporphyrin complexes.2 — Supported by the DFG through SFB 583. — [1] K. Flechtner, A. Kretschmann, H.-P. Steinrück, J.M. Gottfried, J. Am. Chem. Soc. 129 (2007) 12110. — [2] K. Flechtner, A. Kretschmann, L.R. Bradshaw, M.M. Walz, H.-P. Steinrück, J.M. Gottfried, J. Phys. Chem. C 111 (2007) 5821.