Reversible redox reactions in metal-supported porphyrin: the role of spin and oxidation state

Author:

Cojocariu Iulia1ORCID,Carlotto Silvia23ORCID,Zamborlini Giovanni1ORCID,Jugovac Matteo1ORCID,Schio Luca4ORCID,Floreano Luca4ORCID,Casarin Maurizio2ORCID,Feyer Vitaliy15ORCID,Schneider Claus Michael15

Affiliation:

1. Peter Grünberg Institute (PGI-6), Forschungszentrum Jülich GmbH, 52428 Jülich, Germany

2. Dipartimento di Scienze Chimiche, Università degli Studi di Padova, via F. Marzolo 1, 35131 Padova, Italy

3. Institute of Condensed Matter Chemistry and Technologies for Energy (ICMATE), National Research Council (CNR), c/o Department of Chemistry, University of Padova, via F. Marzolo 1, 35131 Padova, Italy

4. CNR-IOM, Lab. TASC, s.s. 14 km 163,5, 34149 Trieste, Italy

5. Fakultät f Physik and Center for Nanointegration Duisburg-Essen (CENIDE), Universität Duisburg-Essen, D-47048 Duisburg, Germany

Abstract

The reduced Co(i) metal ion in the molecular array facilitates the formation of the cobalt–ligand chemical bond already at RT. We demonstrate that molecular reactivity goes beyond the sole presence of unpaired electrons in the valence shell.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry

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