Strong Exchange Couplings Drastically Slow Down Magnetization Relaxation in an Air‐Stable Cobalt(II)‐Radical Single‐Molecule Magnet (SMM)
The energy barrier leading to magnetic bistability in molecular clusters is determined by the magnetic anisotropy of the cluster constituents. By incorporating a highly anisotropic four‐coordinate cobalt(II) building block into a strongly coupled fully air‐ and moisture‐stable three‐spin system, it...
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| Veröffentlicht in: | Angewandte Chemie International Edition Jg. 58; H. 29; S. 9802 - 9806 |
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Wiley Subscription Services, Inc
15.07.2019
John Wiley and Sons Inc |
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| ISSN: | 1433-7851, 1521-3773, 1521-3773 |
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| Abstract | The energy barrier leading to magnetic bistability in molecular clusters is determined by the magnetic anisotropy of the cluster constituents. By incorporating a highly anisotropic four‐coordinate cobalt(II) building block into a strongly coupled fully air‐ and moisture‐stable three‐spin system, it proved possible to suppress under‐barrier Raman processes leading to 350‐fold increase of magnetization relaxation time and pronounced hysteresis. Relaxation times of up to 9 hours at low temperatures were found.
A Co production: The energy barrier leading to magnetic bistability in molecular clusters is determined by the magnetic anisotropy of the cluster constituents. By incorporating a highly anisotropic four‐coordinate cobalt(II) building block into a strongly coupled three‐spin system, it proved possible to increase the magnetization relaxation time by a factor of 350 to almost 9 hours at low temperatures. |
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| AbstractList | The energy barrier leading to magnetic bistability in molecular clusters is determined by the magnetic anisotropy of the cluster constituents. By incorporating a highly anisotropic four-coordinate cobalt(II) building block into a strongly coupled fully air- and moisture-stable three-spin system, it proved possible to suppress under-barrier Raman processes leading to 350-fold increase of magnetization relaxation time and pronounced hysteresis. Relaxation times of up to 9 hours at low temperatures were found.The energy barrier leading to magnetic bistability in molecular clusters is determined by the magnetic anisotropy of the cluster constituents. By incorporating a highly anisotropic four-coordinate cobalt(II) building block into a strongly coupled fully air- and moisture-stable three-spin system, it proved possible to suppress under-barrier Raman processes leading to 350-fold increase of magnetization relaxation time and pronounced hysteresis. Relaxation times of up to 9 hours at low temperatures were found. The energy barrier leading to magnetic bistability in molecular clusters is determined by the magnetic anisotropy of the cluster constituents. By incorporating a highly anisotropic four-coordinate cobalt(II) building block into a strongly coupled fully air- and moisture-stable three-spin system, it proved possible to suppress under-barrier Raman processes leading to 350-fold increase of magnetization relaxation time and pronounced hysteresis. Relaxation times of up to 9 hours at low temperatures were found. The energy barrier leading to magnetic bistability in molecular clusters is determined by the magnetic anisotropy of the cluster constituents. By incorporating a highly anisotropic four‐coordinate cobalt(II) building block into a strongly coupled fully air‐ and moisture‐stable three‐spin system, it proved possible to suppress under‐barrier Raman processes leading to 350‐fold increase of magnetization relaxation time and pronounced hysteresis. Relaxation times of up to 9 hours at low temperatures were found. A Co production: The energy barrier leading to magnetic bistability in molecular clusters is determined by the magnetic anisotropy of the cluster constituents. By incorporating a highly anisotropic four‐coordinate cobalt(II) building block into a strongly coupled three‐spin system, it proved possible to increase the magnetization relaxation time by a factor of 350 to almost 9 hours at low temperatures. |
| Author | Bamberger, Heiko Sarkar, Biprajit Hallmen, Philipp P. Albold, Uta van Slageren, Joris |
| AuthorAffiliation | 1 Institut für Chemie und Biochemie Freie Universität Berlin Fabeckstrasse 34–36 14195 Berlin Germany 2 Institut für Physikalische Chemie Universität Stuttgart Pfaffenwaldring 55 70569 Stuttgart Germany |
| AuthorAffiliation_xml | – name: 2 Institut für Physikalische Chemie Universität Stuttgart Pfaffenwaldring 55 70569 Stuttgart Germany – name: 1 Institut für Chemie und Biochemie Freie Universität Berlin Fabeckstrasse 34–36 14195 Berlin Germany |
| Author_xml | – sequence: 1 givenname: Uta surname: Albold fullname: Albold, Uta organization: Freie Universität Berlin – sequence: 2 givenname: Heiko surname: Bamberger fullname: Bamberger, Heiko organization: Universität Stuttgart – sequence: 3 givenname: Philipp P. surname: Hallmen fullname: Hallmen, Philipp P. organization: Universität Stuttgart – sequence: 4 givenname: Joris orcidid: 0000-0002-0855-8960 surname: van Slageren fullname: van Slageren, Joris email: slageren@ipc.uni-stuttgart.de organization: Universität Stuttgart – sequence: 5 givenname: Biprajit surname: Sarkar fullname: Sarkar, Biprajit email: Biprajit.Sarkar@fu-berlin.de organization: Freie Universität Berlin |
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| SubjectTerms | Anisotropy Bistability Cobalt Communication Communications Coupling (molecular) Couplings hysteresis Low temperature Magnetic anisotropy Magnetization Molecular clusters molecular magnetism Raman process Relaxation time single-molecule magnet |
| Title | Strong Exchange Couplings Drastically Slow Down Magnetization Relaxation in an Air‐Stable Cobalt(II)‐Radical Single‐Molecule Magnet (SMM) |
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