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Single-chain magnet behavior in a finite linear hexanuclear molecule.


ABSTRACT: The careful monitoring of crystallization conditions of a mixture made of a TbIII building block and a substituted nitronyl-nitroxide that typically provides infinite coordination polymers (chains), affords a remarkably stable linear hexanuclear molecule made of six TbIII ions and five NIT radicals. The hexanuclear units are double-bridged by water molecules but ab initio calculations demonstrate that this bridge is inefficient in mediating any magnetic interaction other than a small dipolar antiferromagnetic coupling. Surprisingly the hexanuclears, despite being finite molecules, show a single-chain magnet (SCM) behavior. This results in a magnetic hysteresis at low temperature whose coercive field is almost doubled when compared to the chains. We thus demonstrate that finite linear molecules can display SCM magnetic relaxation, which is a strong asset for molecular data storage purposes because 1D magnetic relaxation is more robust than the relaxation mechanisms observed in single-molecule magnets (SMMs) where under-barrier magnetic relaxation can operate.

SUBMITTER: Houard F 

PROVIDER: S-EPMC8356920 | biostudies-literature | 2021 Aug

REPOSITORIES: biostudies-literature

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The careful monitoring of crystallization conditions of a mixture made of a Tb<sup>III</sup> building block and a substituted nitronyl-nitroxide that typically provides infinite coordination polymers (<i>chains</i>), affords a remarkably stable linear hexanuclear molecule made of six Tb<sup>III</sup> ions and five NIT radicals. The <i>hexanuclear units</i> are double-bridged by water molecules but <i>ab initio</i> calculations demonstrate that this bridge is inefficient in mediating any magnetic  ...[more]

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