Synthesis and Spectroscopic Characterisation of a Heterodinuclear Iron(III)-Copper(II) Complex Based on an Asymmetric Dinucleating Ligand System

被引:11
|
作者
Heims, Florian [1 ]
Mereacre, Valeriu [2 ]
Ciancetta, Antonella [3 ]
Mebs, Stefan [1 ]
Powell, Annie K. [2 ,4 ]
Greco, Claudio [1 ]
Ray, Kallol [1 ]
机构
[1] Humboldt Univ, Dept Chem, D-12489 Berlin, Germany
[2] KIT, Inst Anorgan Chem, D-76131 Karlsruhe, Germany
[3] Lund Univ, Dept Theoret Chem, Ctr Chem, S-22100 Lund, Sweden
[4] KIT, Inst Nanotechnol, D-76021 Karlsruhe, Germany
关键词
Bioinorganic chemistry; Unsymmetric ligands; Heterometallic complexes; Copper; Iron; PURPLE ACID-PHOSPHATASES; REDOX PROPERTIES; RELEVANCE; ENERGY; BOND; MODELS; CORE;
D O I
10.1002/ejic.201200156
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The site-directed generation of a heterodinuclear FeIIICuII complex by using a new asymmetric dinucleating ligand FloH is reported. The iron(III) ion is introduced first on the preferential metal-binding site of the ligand that leads to the formation of the thermodynamically favored five-membered chelate rings upon metal-binding. Copper(II) is introduced in the next step. The stepwise metalation strategy reported here may be extended to the preparation of other heterometallic complexes with the view of avoiding a statistical distribution. Such complexes can offer novel spectroscopic properties, electronic structures, and reactivities in comparison to their homometallic analogues.
引用
收藏
页码:4565 / 4569
页数:5
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