The exceptionally rich coordination chemistry generated by Schiff-base ligands derived from o-vanillin

被引:194
|
作者
Andruh, Marius [1 ]
机构
[1] Univ Bucharest, Fac Chem, Inorgan Chem Lab, Bucharest 020464, Romania
关键词
SINGLE-MOLECULE-MAGNET; CRYSTAL-STRUCTURES; GD-III; DY-III; TB-III; STRUCTURAL DETERMINATION; SLOW-RELAXATION; SYNTHETIC ROUTE; 3D-4F COMPLEXES; TETRA-DECKER;
D O I
10.1039/c5dt02661j
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Ortho-vanillin became very popular in coordination chemistry because of its Schiff bases, which generate a rich variety of complexes, ranging from oligonuclear species to coordination polymers. Some of these organic molecules are particularly useful in metallosupramolecular chemistry for assembling homo-and heterometallic helicates. The Schiff bases obtained using aminoalcohols open the door to the synthesis of homo- and heterometallic clusters with various nuclearities and surprising topologies of the metal centers. Several relevant structural types are reviewed. The heterobinuclear 3d-3d' and 3d-4f complexes are valuable building-blocks for the synthesis of heterotrimetallic systems. Beyond the richness of this chemistry, the complexes obtained from o-vanillin-based Schiff ligands show interesting properties: magnetism, luminescence, chirality, catalysis, cytotoxicity, and ferroelectricity. This paper reviews recent data that illustrate a very fertile and dynamic research field in coordination chemistry and materials science.
引用
收藏
页码:16633 / 16653
页数:21
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