Polynuclear Fen Complexes (n=1, 2, 4, 5) of Polytopic Hydrazone Ligands with Fe(II), Fe(III) and Mixed Oxidation State Combinations

被引:40
作者
Anwar, Muhammad U. [1 ]
Shuvaev, Konstantin V. [1 ]
Dawe, Louise N. [1 ]
Thompson, Laurence K. [1 ]
机构
[1] Mem Univ, Dept Chem, St Johns Newfoundland, NF A1B 3X7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
SPIN-TRANSITION; MOLECULAR MATERIALS; DIAZINE LIGANDS; SQUARE; GRIDS; CLUSTER; MN(II); CROSSOVER; IRON(II); DINUCLEAR;
D O I
10.1021/ic201891h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The iron coordination chemistry of some polytopic hydrazone based ligands is examined. The complexes derive from a general self-assembly strategy, where ligand design can be used to devise specific polymetallic [n X n] grid architectures. However, as part of any complex equilibrium process, oligomeric entities can also occur, particularly when ligand tautomeric flexibility is considered, and examples of mononuclear, dinuclear, tetranuclear, and pentanuclear complexes have been observed within a related class of ligands. In addition, ligand site donor composition can lead to coordination spheres that stabilize both high spin Fe(II) and Fe(III) sites, with evidence for Fe(II) spin crossover. Structural and magnetic properties are examined, which reveal the presence of antiferromagnetic exchange in the polynuclear systems.
引用
收藏
页码:12141 / 12154
页数:14
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