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2,6‐Bis(pyrazol‐3‐yl)pyridine as Meridional Capping Ligand: Synthesis, Characterization, and Crystal Structure of the First Corresponding Hexanuclear Iron(III) Complex
Author(s) -
Plaul Daniel,
Spielberg Eike T.,
Plass Winfried
Publication year - 2010
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.201000075
Subject(s) - chemistry , pyridine , antiferromagnetism , crystallography , ligand (biochemistry) , zonal and meridional , crystal structure , stereochemistry , medicinal chemistry , biochemistry , physics , receptor , atmospheric sciences , geology , condensed matter physics
Based on the 2,6‐bis(pyrazol‐3‐yl)pyridine ligand (H 2 bpp) the hexanuclear iron(III) complex [Fe 6 (bpp) 4 ( μ 3 ‐O) 2 ( μ ‐OMe) 3 ( μ ‐OH)Cl 2 ] ( 1 ) was synthesized. The reaction with iron(II) chloride and additional pyridine leads to the exclusive formation of the complex through self‐assembly process. Six octahedrally coordinated iron atoms are linked through the pyrazolido groups of four H 2 bpp ligands. These are further linked through bridging hydroxido, methoxido, and oxido groups. The complex has been characterized by IR spectroscopy, ESI mass spectrometry, elemental analysis and X‐ray crystallography. Temperature‐dependent magnetic measurements indicate strong antiferromagnetic exchange interaction between the high‐spin iron(III) ions within the complex, which leads to an S = 0 spin ground state. As a result of the two Fe3( μ 3 ‐O) fragments two frustrated exchange pathways are present. In addition the properties of H 2 bpp as a potential capping ligand for the synthesis of heteroleptic trinuclear complexes based on the triaminoguanidine core is investigated.
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