Dinuclear nickel(II) and zinc(II) complexes of 2,6-[N,N'-bis(2-hydroxyphenylmethyl)-N,N'-bis (2-pyridylmethyl)aminomethyl]-4-methylphenol

被引:12
作者
Adams, H [1 ]
Bradshaw, D [1 ]
Fenton, DE [1 ]
机构
[1] Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England
关键词
crystal structure; di-zinc(II) complex; di-nickel(II) complex; heptadentate ligand;
D O I
10.1080/10610270108028297
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The symmetric 'end-off' compartmental proligand 2,6-[N,N'-bis(2-hydroxy-phenylmethyl)-N,N'-bis(2-pyridylmethyl)aminomethyl]-4-methylphenol (H3L) has been used to generate homodinuclear nickel(II) and zinc(II) complexes. The crystal structures of the complexes reveal that the di-nickel(II) complex is donor asymmetric and the di-zinc(II) complex is coordination number asymmetric. In both complexes non-coordinated acetic acid molecules are tightly hydrogen-bonded to the pendant phenols of the ligand generating a double acid salt of the type [CH3COO . . .H . . .L . . .H . . . OOCCH3](3-) in the dinickel complex and a single acid salt of the type [CH3COO . . .H . . .L](3-) in the dizinc complex. In both cases the ligand periphery has been extended to provide a supraligand in which the donor potential of the original ligand has been enhanced.
引用
收藏
页码:513 / 519
页数:7
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