Journal Article FZJ-2021-04763

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

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2021
RSC London ˜[u.a.]œ

Journal of materials chemistry / C 9(37), 12559 - 12565 () [10.1039/D1TC02222A]

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Abstract: On-surface molecular functionalization paved the way for the stabilization of chelated ions in different oxidation and spin states, allowing for the fine control of catalytic and magnetic properties of metalorganic networks. Considering two model systems, a reduced Co(I) and an open-shell Co(II) metal-supported 2D molecular array, we investigate the interplay between the low valence oxidation and unpaired spin state in the molecular reactivity. We show that the redox reaction taking place at the cobalt tetraphenylporphyrin/Cu(100) interface, stabilizing the low-spin Co(I) state with no unpaired electrons in its valence shell, plays a pivotal role in changing the reactivity. This goes beyond the sole presence of unpaired electrons in the valence state of the Co(II) metal–organic species, often designated as being responsible for the reactivity towards small molecules like NO and NO2. The reversible Co–NO2 interaction, established with the Co(I) leads to the stabilization of the Co(III) oxidation state.

Classification:

Contributing Institute(s):
  1. Elektronische Eigenschaften (PGI-6)
Research Program(s):
  1. 5211 - Topological Matter (POF4-521) (POF4-521)

Appears in the scientific report 2021
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Medline ; Creative Commons Attribution-NonCommercial CC BY-NC 3.0 ; OpenAccess ; Allianz-Lizenz / DFG ; Clarivate Analytics Master Journal List ; Current Contents - Engineering, Computing and Technology ; Current Contents - Physical, Chemical and Earth Sciences ; Essential Science Indicators ; IF >= 5 ; JCR ; National-Konsortium ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Datensatz erzeugt am 2021-12-01, letzte Änderung am 2022-09-30


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