Synthesis of complexes with the polydentate ligand N,N′-bis(2-hydroxyphenyl)-pyridine-2,6-dicarboxamide

被引:12
|
作者
Perez, Yolanda [2 ]
Johnson, Andrew L. [1 ]
Raithby, Paul R. [1 ]
机构
[1] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
[2] Univ Rey Juan Carlos, Dept Quim Inorgan & Analit, ESCET, Madrid 28933, Spain
基金
英国工程与自然科学研究理事会;
关键词
Dicarboxamide; Zinc; Nickel; Palladium; Coordination; Crystal structures; BIS-AMIDE LIGAND; CRYSTAL-STRUCTURES; NICKEL(II); COPPER(II); COORDINATION; CHEMISTRY; DINUCLEAR; IRON(III); BEHAVIOR; IONS;
D O I
10.1016/j.poly.2010.10.012
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The pentadentate ligand N,N'-bis(2-hydroxyphenyl)-pyridine-2,6-dicarboxamide (POPYH4) has been used to prepare a variety of new complexes [HNEt3][Zn4Cl(POPYH)(3)] (2), [HNEt3][PdCl(POPYH2)] (3), [HNEt3][Ni(POPYH)] (4) and K[Ni(POPYH)] (5) which show the versatility of this multidentate ligand. The complexes have been characterised spectroscopically and their molecular and crystal structures have been determined by single crystal X-ray diffraction techniques. In these complexes the ligand exhibits different modes of coordination towards different transition metal ions. The structure of triethylammonium salt of the Zn(II) dianion 2 consists of an unusual tetra-zinc core supported by three POPYH ligands each one of which links two adjacent zinc centres through two oxygen and two nitrogen donor atoms. The salt of the square planar Pd(II) anion 3 contains one POPYH2 ligand which coordinates in a tridentate fashion through the two deprotonated amido groups and by the central pyridine nitrogen donor. The two Ni(II) salts 4 and 5 contain the same [Ni(POPYH)] anion in which the square planar Ni(II) centre is chelated by a POPYH ligand through the two deprotonated amido nitrogen atoms, the pyridine nitrogen and a deprotonated hydroxyl group. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:284 / 292
页数:9
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