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Antisymmetric Spin Exchange in a μ-1,2-Peroxodicopper(II) Complex with an Orthogonal Cu–O–O–Cu Arrangement and S = 1 Spin Ground State Characterized by THz-EPR
[Image: see text] A unique type of Cu(2)/O(2) adduct with orthogonal (close to 90°) Cu–O–O–Cu arrangement has been proposed for initial stages of O(2) binding at biological type III dicopper sites, and targeted ligand design has now allowed us to emulate such an adduct in a pyrazolate-based μ-η(1):η...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131480/ https://www.ncbi.nlm.nih.gov/pubmed/35647586 http://dx.doi.org/10.1021/jacsau.2c00139 |
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author | Lohmiller, Thomas Spyra, Can-Jerome Dechert, Sebastian Demeshko, Serhiy Bill, Eckhard Schnegg, Alexander Meyer, Franc |
author_facet | Lohmiller, Thomas Spyra, Can-Jerome Dechert, Sebastian Demeshko, Serhiy Bill, Eckhard Schnegg, Alexander Meyer, Franc |
author_sort | Lohmiller, Thomas |
collection | PubMed |
description | [Image: see text] A unique type of Cu(2)/O(2) adduct with orthogonal (close to 90°) Cu–O–O–Cu arrangement has been proposed for initial stages of O(2) binding at biological type III dicopper sites, and targeted ligand design has now allowed us to emulate such an adduct in a pyrazolate-based μ-η(1):η(1)-peroxodicopper(II) complex (2) with Cu–O–O–Cu torsion φ of 87°, coined (⊥)P intermediate. Full characterization of 2, including X-ray diffraction (d(O–O) = 1.452 Å) and Raman spectroscopy (ν̃(O–O) = 807 cm(–1)), completes a series of closely related Cu(2)/O(2) intermediates featuring μ-η(1):η(1)-peroxodicopper(II) cores with φ ranging from 55° (A, cis-peroxo (C)P; A. Brinkmeieret al., J. Am. Chem. Soc.2021, 143, 1036134191490) via 87° (2, (⊥)P type) up to 104° (B, approaching trans-peroxo (T)P; N. Kindermannet al., Angew. Chem., Int. Ed.2015, 54, 1738). SQUID magnetometry revealed ferromagnetic interaction of the Cu(II) ions and a triplet (S(t) = 1) ground state in 2. Frequency-domain THz-EPR has been employed to quantitatively investigate the spin systems of 2 and B. Magnetic transitions within the triplet ground states confirmed their substantial zero-field splittings (ZFS) suggested by magnetometry. Formally forbidden triplet-to-singlet transitions at 56 (2) and 157 cm(–1) (B), which are in agreement with the exchange coupling strengths J(iso) inferred from SQUID data, are reported for the first time for coupled dicopper(II) complexes. Rigorous analysis by spin-Hamiltonian-based simulations attributed the corresponding nonzero transition probabilities and the ZFS to substantial antisymmetric (Dzyaloshinskii–Moriya) exchange d and provided robust values and orientations for the d, J, and g tensors. These interactions can be correlated with the Cu–O–O–Cu geometries, revealing a linear increase of J(iso) with the Cu–O–O–Cu torsion and a strong linear decrease with the Cu–O–O angle. Relevance of the (⊥)P intermediate for O(2) activation at type III dicopper sites and a potential role of antisymmetric exchange in the concomitant intersystem crossing are proposed. |
format | Online Article Text |
id | pubmed-9131480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91314802022-05-26 Antisymmetric Spin Exchange in a μ-1,2-Peroxodicopper(II) Complex with an Orthogonal Cu–O–O–Cu Arrangement and S = 1 Spin Ground State Characterized by THz-EPR Lohmiller, Thomas Spyra, Can-Jerome Dechert, Sebastian Demeshko, Serhiy Bill, Eckhard Schnegg, Alexander Meyer, Franc JACS Au [Image: see text] A unique type of Cu(2)/O(2) adduct with orthogonal (close to 90°) Cu–O–O–Cu arrangement has been proposed for initial stages of O(2) binding at biological type III dicopper sites, and targeted ligand design has now allowed us to emulate such an adduct in a pyrazolate-based μ-η(1):η(1)-peroxodicopper(II) complex (2) with Cu–O–O–Cu torsion φ of 87°, coined (⊥)P intermediate. Full characterization of 2, including X-ray diffraction (d(O–O) = 1.452 Å) and Raman spectroscopy (ν̃(O–O) = 807 cm(–1)), completes a series of closely related Cu(2)/O(2) intermediates featuring μ-η(1):η(1)-peroxodicopper(II) cores with φ ranging from 55° (A, cis-peroxo (C)P; A. Brinkmeieret al., J. Am. Chem. Soc.2021, 143, 1036134191490) via 87° (2, (⊥)P type) up to 104° (B, approaching trans-peroxo (T)P; N. Kindermannet al., Angew. Chem., Int. Ed.2015, 54, 1738). SQUID magnetometry revealed ferromagnetic interaction of the Cu(II) ions and a triplet (S(t) = 1) ground state in 2. Frequency-domain THz-EPR has been employed to quantitatively investigate the spin systems of 2 and B. Magnetic transitions within the triplet ground states confirmed their substantial zero-field splittings (ZFS) suggested by magnetometry. Formally forbidden triplet-to-singlet transitions at 56 (2) and 157 cm(–1) (B), which are in agreement with the exchange coupling strengths J(iso) inferred from SQUID data, are reported for the first time for coupled dicopper(II) complexes. Rigorous analysis by spin-Hamiltonian-based simulations attributed the corresponding nonzero transition probabilities and the ZFS to substantial antisymmetric (Dzyaloshinskii–Moriya) exchange d and provided robust values and orientations for the d, J, and g tensors. These interactions can be correlated with the Cu–O–O–Cu geometries, revealing a linear increase of J(iso) with the Cu–O–O–Cu torsion and a strong linear decrease with the Cu–O–O angle. Relevance of the (⊥)P intermediate for O(2) activation at type III dicopper sites and a potential role of antisymmetric exchange in the concomitant intersystem crossing are proposed. American Chemical Society 2022-05-06 /pmc/articles/PMC9131480/ /pubmed/35647586 http://dx.doi.org/10.1021/jacsau.2c00139 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Lohmiller, Thomas Spyra, Can-Jerome Dechert, Sebastian Demeshko, Serhiy Bill, Eckhard Schnegg, Alexander Meyer, Franc Antisymmetric Spin Exchange in a μ-1,2-Peroxodicopper(II) Complex with an Orthogonal Cu–O–O–Cu Arrangement and S = 1 Spin Ground State Characterized by THz-EPR |
title | Antisymmetric Spin Exchange in a μ-1,2-Peroxodicopper(II)
Complex with an Orthogonal Cu–O–O–Cu Arrangement
and S = 1 Spin Ground State Characterized by THz-EPR |
title_full | Antisymmetric Spin Exchange in a μ-1,2-Peroxodicopper(II)
Complex with an Orthogonal Cu–O–O–Cu Arrangement
and S = 1 Spin Ground State Characterized by THz-EPR |
title_fullStr | Antisymmetric Spin Exchange in a μ-1,2-Peroxodicopper(II)
Complex with an Orthogonal Cu–O–O–Cu Arrangement
and S = 1 Spin Ground State Characterized by THz-EPR |
title_full_unstemmed | Antisymmetric Spin Exchange in a μ-1,2-Peroxodicopper(II)
Complex with an Orthogonal Cu–O–O–Cu Arrangement
and S = 1 Spin Ground State Characterized by THz-EPR |
title_short | Antisymmetric Spin Exchange in a μ-1,2-Peroxodicopper(II)
Complex with an Orthogonal Cu–O–O–Cu Arrangement
and S = 1 Spin Ground State Characterized by THz-EPR |
title_sort | antisymmetric spin exchange in a μ-1,2-peroxodicopper(ii)
complex with an orthogonal cu–o–o–cu arrangement
and s = 1 spin ground state characterized by thz-epr |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131480/ https://www.ncbi.nlm.nih.gov/pubmed/35647586 http://dx.doi.org/10.1021/jacsau.2c00139 |
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