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Rod-shaped [Mn6] complexes as single-molecule magnets
Authors:Katie J Heroux  Sonali J Shah  Motohiro Nakano  David N Hendrickson
Institution:a Department of Chemistry and Biochemistry, University of California at San Diego, La Jolla, CA 92093, USA
b Quantum Design, San Diego, CA 92121, USA
c Division of Applied Chemistry, Osaka University, Suita, Osaka 565-0871, Japan
Abstract:The preparation, X-ray crystal structures, and magnetic properties of four new rod-shaped hexanuclear Mn clusters Mn6(O2CCH3)6(EdeaH)2(tmp)2] (1), Mn6(O2CCH3)6(mdeaH)2(tmp)2] (2), Mn6(O2CCF3)6(teaH2)2(tmp)2]·2MeCN (3) and Mn6(O2CPh)6(EdeaH)2(tmp)2]·2Et2O (4), where teaH3 is triethanolamine and tmpH3 is the tris-hydroxymethyl propane ligand, are reported. DC magnetization data along with AC magnetic susceptibility studies show that these complexes have weak antiferromagnetic coupling, appreciable magnetoanisotropy, and ground states of up to S = 4. Though all four complexes show a frequency-dependent out-of-phase signal in the AC susceptibility, a characteristic of single-molecule magnets (SMMs), only complexes 1, 2, and 4 are likely to be SMMs with ground states ranging from S = 2 to S = 4. Complex 3 shows the weakest AC signal and the lowest spin ground state of S ≈ 1, likely due to small structural differences and intermolecular interactions.
Keywords:Single-molecule magnets  Magnetoanisotropy  X-ray crystal structure  Mixed-valent  Magnetic susceptibility
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