Calix[4]arene-Supported Mononuclear Lanthanide Single-Molecule Magnet

被引:56
|
作者
Gao, Feng [1 ,2 ]
Cui, Long [1 ]
Song, You [1 ]
Li, Yi-Zhi [1 ]
Zuo, Jing-Lin [1 ]
机构
[1] Nanjing Univ, State Key Lab Coordinat Chem, Sch Chem & Chem Engn, Nanjing Natl Lab Microstruct, Nanjing 210093, Jiangsu, Peoples R China
[2] Jiangsu Normal Univ, Sch Chem & Chem Engn, Jiangsu Key Lab Green Synthet Chem Funct Mat, Xuzhou 221116, Peoples R China
基金
中国国家自然科学基金;
关键词
ION MAGNETS; COMPLEXES; RELAXATION; ANISOTROPY; BEHAVIOR; LIGAND; FIELD; MAGNETIZATION; SERIES; METAL;
D O I
10.1021/ic4026624
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three new single paramagnetic lanthanide-based complexes, [Ln(L)(L-OEt)] (Ln(3+) = Dy3+, Tb3+, and Ho3+), are synthesized with the multidentate calix[4]arene ligand H2L (H2L = 5,11,17,23-tetrakis(1,1-dimethylethyl)-25,27-dihydroxy-26,28-dimethoxycalix[4]arene) and Klaui's tripodal ligand L-OEt(-) (L-OEt(-) = (eta(5)-cyclopentadienyl)tris(diethylphosphito-p)cobaltate(III)). All of the complexes have been characterized by single crystal X-ray diffraction analysis, thermal stability, absorption spectra, and magnetization measurements. The magnetic properties and magneto-structural correlation in this seven-coordinated system are investigated. The dysprosium complex 1 shows typical single-molecule magnetic behavior with characteristic magnetic hysteresis loops and the slow relaxation of magnetization.
引用
收藏
页码:562 / 567
页数:6
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