Zero‐Valent Nickel Stabilized in Surface‐Supported Metal–Organic Chains

The stabilization of zero-valent nickel Ni(0) centers in extended coordination networks remains a major challenge due to their pronounced reactivity and susceptibility to oxidation. Here, we demonstrate that linear coordination confinement within a surface-supported metal-organic chain enables the stabilization of Ni(0) atoms on Ag(100). The symmetry of 9,10-dicyanoanthracene (DCA), combined with substrate templating effects, directs the formation of an ordered linear Ni-DCA coordination motif. Spectroscopic measurements provide unambiguous evidence for a formal Ni(0) oxidation state, representing a rare realization of a zero-valent transition metal center within an extended, atomically defined system. The electronic structure is governed by hybridization between Ni 3d orbitals and the π-system of DCA, resulting in an anisotropic electronic dispersion with predominantly one-dimensional character. These results establish linear coordination as a strategy to stabilize reactive, low-valent metal centers in surface-supported metal-organic architectures.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-07-24
DOI
https://doi.org/10.1002/anie.1508970
Primary Topic
Surface Chemistry and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Zero‐Valent Nickel Stabilized in Surface‐Supported Metal–Organic Chains

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Angewandte Chemie International Edition
Surface Chemistry and Catalysis
article

Zero‐Valent Nickel Stabilized in Surface‐Supported Metal–Organic Chains

Peter Puschnig, Giovanni Zamborlini, Daniel Baranowski, Dominik Brandstetter, Claus M. Schneider, Martin Sterrer, Vitaliy Feyer, Simone Mearini, Yan Yan Grisan Qiu, Olga Resel, Mira S. Arndt
article en

Abstract

The stabilization of zero-valent nickel Ni(0) centers in extended coordination networks remains a major challenge due to their pronounced reactivity and susceptibility to oxidation. Here, we demonstrate that linear coordination confinement within a surface-supported metal-organic chain enables the stabilization of Ni(0) atoms on Ag(100). The symmetry of 9,10-dicyanoanthracene (DCA), combined with substrate templating effects, directs the formation of an ordered linear Ni-DCA coordination motif. Spectroscopic measurements provide unambiguous evidence for a formal Ni(0) oxidation state, representing a rare realization of a zero-valent transition metal center within an extended, atomically defined system. The electronic structure is governed by hybridization between Ni 3d orbitals and the π-system of DCA, resulting in an anisotropic electronic dispersion with predominantly one-dimensional character. These results establish linear coordination as a strategy to stabilize reactive, low-valent metal centers in surface-supported metal-organic architectures.

Angewandte Chemie International Edition
Pacific Northwest National Laboratory (US), Forschungszentrum Jülich (DE), TU Dortmund University (DE), Ernst Ruska Centre (DE), Nawi Graz (AT), University of Duisburg-Essen (DE), University of California, Davis (US)
Deutsche Forschungsgemeinschaft, European Research Council
Openalex Percentile: Top 16%
Surface Chemistry and Catalysis
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