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Spin-Phonon Coupling and Slow-Magnetic Relaxation in Pristine Ferrocenium.


ABSTRACT: We report the spin dynamic properties of non-substituted ferrocenium complexes. Ferrocenium shows a field-induced single-molecule magnet behaviour in DMF solution while cobaltocene lacks slow spin relaxation neither in powder nor in solution. Multireference quantum mechanical calculations give a non-Aufbau orbital occupation for ferrocenium with small first excitation energy that agrees with the relatively large measured magnetic anisotropy for a transition metal S=1/2 system. The analysis of the spin relaxation shows an important participation of quantum tunnelling, Raman, direct and local-mode mechanisms which depend on temperature and the external field conditions. The calculation of spin-phonon coupling constants for the vibrational modes shows that the first vibrational mode, despite having a low spin-phonon constant, is the most efficient process for the spin relaxation at low temperatures. In such conditions, vibrational modes with higher spin-phonon coupling constants are not populated. Additionally, the vibrational energy of this first mode is in excellent agreement with the experimental fitted value obtained from the local-mode mechanism.

SUBMITTER: Amoza M 

PROVIDER: S-EPMC9298439 | biostudies-literature | 2021 Nov

REPOSITORIES: biostudies-literature

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Spin-Phonon Coupling and Slow-Magnetic Relaxation in Pristine Ferrocenium.

Amoza Martín M   Maxwell Lindley L   Aliaga-Alcalde Núria N   Gómez-Coca Silvia S   Ruiz Eliseo E  

Chemistry (Weinheim an der Bergstrasse, Germany) 20211027 66


We report the spin dynamic properties of non-substituted ferrocenium complexes. Ferrocenium shows a field-induced single-molecule magnet behaviour in DMF solution while cobaltocene lacks slow spin relaxation neither in powder nor in solution. Multireference quantum mechanical calculations give a non-Aufbau orbital occupation for ferrocenium with small first excitation energy that agrees with the relatively large measured magnetic anisotropy for a transition metal S=1/2 system. The analysis of th  ...[more]

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