Importance of Axial Symmetry in Elucidating Lanthanide-Transition Metal Interactions

In this paper, we experimentally study and model the electron donating character of an axial diamagnetic Pd ion in four metalloligated lanthanide complexes of formula [PPh ][Ln{Pd(SAc) } ] (SAc = thioacetate, Ln = Tb, Dy, Ho, and Er). A global model encompassing inelastic neutron scattering, torque...

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Published in:Inorganic chemistry Vol. 59; no. 1; p. 235
Main Authors: Bonde, Niels A, Petersen, Jonatan B, Sørensen, Mikkel A, Nielsen, Ulla G, Fåk, Björn, Rols, Stéphane, Ollivier, Jacques, Weihe, Høgni, Bendix, Jesper, Perfetti, Mauro
Format: Journal Article
Language:English
Published: United States 06.01.2020
ISSN:1520-510X, 1520-510X
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Abstract In this paper, we experimentally study and model the electron donating character of an axial diamagnetic Pd ion in four metalloligated lanthanide complexes of formula [PPh ][Ln{Pd(SAc) } ] (SAc = thioacetate, Ln = Tb, Dy, Ho, and Er). A global model encompassing inelastic neutron scattering, torque magnetometry, and dc magnetometry allows to precisely determine the energy level structure of the complexes. Solid state nuclear magnetic resonance reveals a less donating character of Pd compared to the previously reported isostructural Pt -based complexes. Consequently, all complexes invariably show a lower crystal field strength compared to their Pt -analogues. The dynamic properties show an enhanced single molecule magnet behavior due to the suppression of quantum tunneling, in agreement with our model.
AbstractList In this paper, we experimentally study and model the electron donating character of an axial diamagnetic Pd ion in four metalloligated lanthanide complexes of formula [PPh ][Ln{Pd(SAc) } ] (SAc = thioacetate, Ln = Tb, Dy, Ho, and Er). A global model encompassing inelastic neutron scattering, torque magnetometry, and dc magnetometry allows to precisely determine the energy level structure of the complexes. Solid state nuclear magnetic resonance reveals a less donating character of Pd compared to the previously reported isostructural Pt -based complexes. Consequently, all complexes invariably show a lower crystal field strength compared to their Pt -analogues. The dynamic properties show an enhanced single molecule magnet behavior due to the suppression of quantum tunneling, in agreement with our model.
In this paper, we experimentally study and model the electron donating character of an axial diamagnetic Pd2+ ion in four metalloligated lanthanide complexes of formula [PPh4][Ln{Pd(SAc)4}2] (SAc- = thioacetate, Ln = Tb, Dy, Ho, and Er). A global model encompassing inelastic neutron scattering, torque magnetometry, and dc magnetometry allows to precisely determine the energy level structure of the complexes. Solid state nuclear magnetic resonance reveals a less donating character of Pd2+ compared to the previously reported isostructural Pt2+-based complexes. Consequently, all complexes invariably show a lower crystal field strength compared to their Pt2+-analogues. The dynamic properties show an enhanced single molecule magnet behavior due to the suppression of quantum tunneling, in agreement with our model.In this paper, we experimentally study and model the electron donating character of an axial diamagnetic Pd2+ ion in four metalloligated lanthanide complexes of formula [PPh4][Ln{Pd(SAc)4}2] (SAc- = thioacetate, Ln = Tb, Dy, Ho, and Er). A global model encompassing inelastic neutron scattering, torque magnetometry, and dc magnetometry allows to precisely determine the energy level structure of the complexes. Solid state nuclear magnetic resonance reveals a less donating character of Pd2+ compared to the previously reported isostructural Pt2+-based complexes. Consequently, all complexes invariably show a lower crystal field strength compared to their Pt2+-analogues. The dynamic properties show an enhanced single molecule magnet behavior due to the suppression of quantum tunneling, in agreement with our model.
Author Ollivier, Jacques
Bonde, Niels A
Weihe, Høgni
Bendix, Jesper
Fåk, Björn
Perfetti, Mauro
Sørensen, Mikkel A
Petersen, Jonatan B
Rols, Stéphane
Nielsen, Ulla G
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  givenname: Jonatan B
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  organization: Department of Chemistry , University of Copenhagen , Universitetsparken 5 , DK-2100 Copenhagen , Denmark
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  organization: Department of Chemistry , University of Copenhagen , Universitetsparken 5 , DK-2100 Copenhagen , Denmark
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  orcidid: 0000-0003-1255-2868
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  surname: Perfetti
  fullname: Perfetti, Mauro
  organization: Department of Chemistry , University of Copenhagen , Universitetsparken 5 , DK-2100 Copenhagen , Denmark
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Snippet In this paper, we experimentally study and model the electron donating character of an axial diamagnetic Pd ion in four metalloligated lanthanide complexes of...
In this paper, we experimentally study and model the electron donating character of an axial diamagnetic Pd2+ ion in four metalloligated lanthanide complexes...
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