Solvent Responsive Magnetic Dynamics of a Dinuclear Dysprosium Single‐Molecule Magnet
Identifieur interne : 000936 ( Main/Exploration ); précédent : 000935; suivant : 000937Solvent Responsive Magnetic Dynamics of a Dinuclear Dysprosium Single‐Molecule Magnet
Auteurs : Min Ren [République populaire de Chine] ; Song-Song Bao [République populaire de Chine] ; Norihisa Hoshino [Japon] ; Tomoyuki Akutagawa [Japon] ; Bingwu Wang [République populaire de Chine] ; Yu-Chen Ding [République populaire de Chine] ; Shiqiang Wei [République populaire de Chine] ; Li-Min Zheng [République populaire de Chine]Source :
- Chemistry – A European Journal [ 0947-6539 ] ; 2013-07-15.
Abstract
A new dysprosium(III) phosphonate dimer {Dy(notpH4)(NO3)(H2O)}2⋅8 H2O (1) [notpH6=1,4,7‐triazacyclononane‐1,4,7‐triyl‐tris(methylenephosphonic acid)] that contains two equivalent DyIII ions with a three‐capped trigonal prism environment is reported. Complex 1 can be transformed into {Dy(notpH4)(NO3)(H2O)}2 (2) in a reversible manner by desorption and absorption of solvent water at ambient temperature. This process is accompanied by a large dielectric response. Magnetic studies reveal that both 1 and 2 show thermally activated magnetization relaxation as expected for single‐molecule magnets. Moreover, the magnetic dynamics of the two compounds can be manipulated by controlling the number of solvent molecules at room temperature.
Under control! The magnetic dynamics of a dinuclear single‐molecule magnet {Dy(notpH4)(NO3)(H2O)}2⋅ 8 H2O (see figure; notpH6=1,4,7‐triazacyclononane‐1,4,7‐triyltris(methylenephosphonic acid)) can be manipulated by controlling the number of solvent molecules at room temperature.
Url:
DOI: 10.1002/chem.201300497
Affiliations:
- Japon, République populaire de Chine
- Pékin, Région de Tōhoku
- Pékin, Sendai
- Université de Pékin, Université du Tōhoku
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<front><div type="abstract" xml:lang="en">A new dysprosium(III) phosphonate dimer {Dy(notpH4)(NO3)(H2O)}2⋅8 H2O (1) [notpH6=1,4,7‐triazacyclononane‐1,4,7‐triyl‐tris(methylenephosphonic acid)] that contains two equivalent DyIII ions with a three‐capped trigonal prism environment is reported. Complex 1 can be transformed into {Dy(notpH4)(NO3)(H2O)}2 (2) in a reversible manner by desorption and absorption of solvent water at ambient temperature. This process is accompanied by a large dielectric response. Magnetic studies reveal that both 1 and 2 show thermally activated magnetization relaxation as expected for single‐molecule magnets. Moreover, the magnetic dynamics of the two compounds can be manipulated by controlling the number of solvent molecules at room temperature.</div>
<div type="abstract" xml:lang="en">Under control! The magnetic dynamics of a dinuclear single‐molecule magnet {Dy(notpH4)(NO3)(H2O)}2⋅ 8 H2O (see figure; notpH6=1,4,7‐triazacyclononane‐1,4,7‐triyltris(methylenephosphonic acid)) can be manipulated by controlling the number of solvent molecules at room temperature.</div>
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