Synthesis, Structure and Magnetic Properties of an Unusual Oligonuclear Iron(III)-Cobalt(III) Compound with Oxido-, Sulfato- and Cyanido-Bridging Ligands

Author

F. Setifi
Z. Setifi
P. Konieczny
C. Glidewell
S. Benmansour
C. J. Gomez-Garcia
Fernande Grandjean, Missouri University of Science and TechnologyFollow
Gary J. Long, Missouri University of Science and TechnologyFollow
R. Pelka
J. Reedijk

Abstract

The synthesis, characterization, structure and magnetic properties of a hexametallic mixed-metal iron(III)-cobalt(III) compound are described. The compound has been characterized by standard spectroscopic and analytical methods to determine its composition. Single-crystal X-ray diffraction has shown that the asymmetric unit consists of discrete dinuclear dicationic units of {(µ-oxido-µ-[sulfato-O1,O₂])bis[tris(2-pyridyl-methyl)amineiron(III)]}²⁺, herein designated as Fe12, and two half-dinuclear dianionic units of {(µ-oxido)bis[(µ-cyanido-κN-pentacyanidocobaltato(III))(tris(2-pyridyl-methyl)-amine)iron(III)]}^2- units, herein designated as Fe33a and Fe44b, generating the overall composition Co₂Fe₄O₂(CN)₁₂(tpa)₄, 1, where tpa is tris(2-pyridyl-methyl)amine. X-ray structural results and thermogravimetric and differential scanning calorimetry measurements also indicate that the compound, depending upon its history, may contain up to nine interstitial waters of hydration, herein designated as 1(H₂O)₉. In the dinuclear dicationic unit, the bridging Fe-O-Fe bond in Fe12 is bent and there is also an Fe-O-S-O-Fe sulfato-based bridge with an angle of 132.8°. In contrast, in the two dinuclear dianionic units, Fe33a and Fe44b, the Fe-O-Fe bond angle is crystallographically constrained to be 180°. The Co-CN-Fe bonds are almost co-linear, with Co-C-N angles of 176° and C-N-Fe angles of 169°. In each species the tpa ligand is tripodal tetradentate with the tertiary amine trans to the sulfato ligand or to the cyanide ligand in the dianions or the bridged oxido ligand in the dications. Bond lengths and angles are all in the typical range for Fe(III) and Co(III) compounds. The magnetic behavior of 1(H₂O)₉, obtained upon cooling from 300 to 2 K, reveals a strong antiferromagnetic interaction between the Fe(III) ions in each dinuclear unit. Attempts to discriminate between the two Fe(III) dinuclear units in 1(H₂O)₉ have in all cases led to two very different Heisenberg isotropic exchange coupling constants, namely J = −220(2) and -716(32) cm^-1 for 1(H₂O)₉; i.e. one of the dinuclear units, probably the Fe12 unit, is so strongly antiferromagnetically coupled that it is close to diamagnetic between 2 and ca. 250 K and has a Heisenberg S = 0 ground state.

Recommended Citation

F. Setifi and Z. Setifi and P. Konieczny and C. Glidewell and S. Benmansour and C. J. Gomez-Garcia and F. Grandjean and G. J. Long and R. Pelka and J. Reedijk, "Synthesis, Structure and Magnetic Properties of an Unusual Oligonuclear Iron(III)-Cobalt(III) Compound with Oxido-, Sulfato- and Cyanido-Bridging Ligands," Polyhedron, vol. 157, pp. 558 - 566, Elsevier Ltd, Jan 2019.

The definitive version is available at https://doi.org/10.1016/j.poly.2018.10.021

Department(s)

Chemistry

Research Center/Lab(s)

Center for High Performance Computing Research

Keywords and Phrases

Antiferromagnetism; Cobalt(III); Cyanide; Iron(III); Oxido-bridges

International Standard Serial Number (ISSN)

0277-5387

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 2019 Elsevier Ltd, All rights reserved.

Publication Date

01 Jan 2019