Metal−organic coordination interactions are prime candidates for the formation of self-assembled, nanometer-scale periodic networks with room-temperature structural stability. We present X-ray photoelectron spectroscopy measurements of such networks at the Cu(100) surface which provide clear evidence for genuine metal−organic coordination. This is evident as binding energy shifts in the O 1s and Fe 3p photoelectron peaks, corresponding to O and Fe atoms involved in the coordination. Our results provide the first clear evidence for charge-transfer coordination in metal−organic networks at surfaces and demonstrate a well-defined oxidation state for the coordinated Fe ions
Rational design of highly stable and active metal catalysts requires a deep understanding of metal–s...
The adsorption of tetrahydroxyquinone (THQ) on the Cu(111) surface at different temperatures gives r...
We report the construction of complex metal-organic assemblies at surfaces using concepts from coord...
Metal-organic coordination interactions are prime candidates for the formation of self-assembled, na...
The high chemical reactivity of unsaturated metal sites is a key factor for the development of novel...
The high chemical reactivity of unsaturated metal sites is a key factor for the development of novel...
The high chemical reactivity of unsaturated metalsites is a key factor for the development of novel ...
Metal–ligand complexation at surfaces utilizing redox‐active ligands has been demonstrated to produc...
International audienceWe have investigated the role played by the atomic structure and reactivity of...
We describe the formation of lanthanide–organic coordination networks and complexes under ultra-high...
We report the formation of an Fe-DCNQI (DCNQI = dicyano-p-quinodiimine) coordination network on the ...
Resumen del trabajo presentado a la XXXVII Reunión Bienal de la Real Sociedad Española de Física cel...
The structure−electronic structure relationship of nonmetalated meso-tetraphenyl porphyrin (2H-TPP) ...
We study the formation of a coordination network consisting of the organic pyridine-based 2,4,6-tris...
A novel approach of identifying metal atoms within a metal–organic surface coordination network usin...
Rational design of highly stable and active metal catalysts requires a deep understanding of metal–s...
The adsorption of tetrahydroxyquinone (THQ) on the Cu(111) surface at different temperatures gives r...
We report the construction of complex metal-organic assemblies at surfaces using concepts from coord...
Metal-organic coordination interactions are prime candidates for the formation of self-assembled, na...
The high chemical reactivity of unsaturated metal sites is a key factor for the development of novel...
The high chemical reactivity of unsaturated metal sites is a key factor for the development of novel...
The high chemical reactivity of unsaturated metalsites is a key factor for the development of novel ...
Metal–ligand complexation at surfaces utilizing redox‐active ligands has been demonstrated to produc...
International audienceWe have investigated the role played by the atomic structure and reactivity of...
We describe the formation of lanthanide–organic coordination networks and complexes under ultra-high...
We report the formation of an Fe-DCNQI (DCNQI = dicyano-p-quinodiimine) coordination network on the ...
Resumen del trabajo presentado a la XXXVII Reunión Bienal de la Real Sociedad Española de Física cel...
The structure−electronic structure relationship of nonmetalated meso-tetraphenyl porphyrin (2H-TPP) ...
We study the formation of a coordination network consisting of the organic pyridine-based 2,4,6-tris...
A novel approach of identifying metal atoms within a metal–organic surface coordination network usin...
Rational design of highly stable and active metal catalysts requires a deep understanding of metal–s...
The adsorption of tetrahydroxyquinone (THQ) on the Cu(111) surface at different temperatures gives r...
We report the construction of complex metal-organic assemblies at surfaces using concepts from coord...