Thiacalix[4]arene-Supported Planar Ln4 (Ln = TbIII, DyIII) Clusters: Toward Luminescent and Magnetic Bifunctional Materials

被引:151
作者
Bi, Yanfeng [1 ,3 ]
Wang, Xiu-Teng [2 ]
Liao, Wuping [1 ]
Wang, Xinwu [1 ]
Deng, Ruiping [1 ]
Zhang, Hongjie [1 ]
Gao, Song [2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
[2] Peking Univ, Natl Lab Mol Sci, State Key Lab Rare Earth Mat Chem & Applicat, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[3] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
SINGLE-MOLECULE-MAGNET; COORDINATION POLYMERS; MULTIFUNCTIONAL MATERIALS; DYSPROSIUM TRIANGLES; TRANSITION-METAL; COMPLEXES; BEHAVIOR; IONS; PHOTOLUMINESCENCE; RELAXATION;
D O I
10.1021/ic9017807
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This paper reports the syntheses, crystal structures, and luminescent and magnetic properties of four tetranuclear Tb-III (1 and 3) and Dy-III (2 and 4) complexes supported by p-phenylthiacalix[4]arene (H(4)PTC4A) and p-tert-butylthiacalix-[4]arene (H(4)TC4A). All four frameworks can be formulated as [Ln(4)(III)(PTC4A/TC4A)(2)(mu(4)-OH)Cl-3(CH3OH)(2)(H2O)(3)], and some methanol and water solvent molecules are occupied in the interstices. The compounds are featured with a sandwichlike unit constructed by two tail-to-tail calixarene molecules and a planar tetragonal (mu(4)-OH)Ln(4) cluster. The photoluminescent analyses suggest that there is an efficient ligand-to-Ln(III) energy transfer for compounds 1-3 and H(4)PTC4A is a more efficient "antenna" than H(4)TC4A. The Dy-III compounds exhibit slow magnetic relaxation behavior of single-molecule magnet nature. The substitution of the t-Bu group with a phenyl group at the up-rim of thiacalix[4]arene leads to different extended structures and physical properties of as-synthesized compounds.
引用
收藏
页码:11743 / 11747
页数:5
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