Exchange coupling and single molecule magnetism in redox-active tetraoxolene-bridged dilanthanide complexes

被引:88
作者
Zhang, Peng [1 ]
Perfetti, Mauro [1 ,2 ]
Kern, Michal [1 ]
Hallmen, Philipp P. [1 ]
Ungur, Liviu [3 ]
Lenz, Samuel [1 ]
Ringenberg, Mark R. [4 ]
Frey, Wolfgang [5 ]
Stoll, Hermann [6 ]
Rauhut, Guntram [6 ]
van Slageren, Joris [1 ]
机构
[1] Univ Stuttgart, Inst Phys Chem, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
[2] Univ Copenhagen, Dept Chem, Univ Pk 5, DK-2100 Copenhagen, Denmark
[3] Katholieke Univ Leuven, INPAC Inst Nanoscale Phys & Chem, Theory Nanomat Grp, B-3001 Leuven, Belgium
[4] Univ Stuttgart, Inst Anorgan Chem, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
[5] Univ Stuttgart, Inst Organ Chem, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
[6] Univ Stuttgart, Inst Theoret Chem, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
关键词
RARE-EARTH COMPLEXES; HIGH-FIELD EPR; SEMIQUINONATO COMPLEX; URANIUM(III) COMPLEXES; ION MAGNET; RELAXATION; ANISOTROPY; BLOCKING; BEHAVIOR; MAGNETIZATION;
D O I
10.1039/c7sc04873d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tetraoxolene radical-bridged lanthanide SMM systems were prepared for the first time by reduction of the respective neutral compounds. Magnetic measurements reveal the profound influence of the radical center on magnetic behavior. Strong magnetic couplings are revealed in the radical species, which switch on SMM behavior under zero applied field for Dy-III and Tb-III compounds. HFEPR spectra unravel the contributions of the magnetic coupling and the magnetic anisotropy. For Gd-III this results in much more accurate magnetic coupling parameters with respect to bulk magnetic measurements.
引用
收藏
页码:1221 / 1230
页数:10
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