Strong Exchange Coupling in a Trimetallic Radical‐Bridged Cobalt(II)‐Hexaazatrinaphthylene Complex |
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Authors: | Dr Jani O Moilanen Dr Nicholas F Chilton Dr Benjamin M Day Dr Thomas Pugh Prof Dr Richard A Layfield |
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Institution: | 1. School of Chemistry, The University of Manchester, Manchester, UK;2. Department of Chemistry, University of Jyvaskala, Jyvaskala, Finland |
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Abstract: | Reducing hexaazatrinaphthylene (HAN) with potassium in the presence of 18‐c‐6 produces {K(18‐c‐6)}HAN], which contains the S=1/2 radical HAN].?. The HAN].? radical can be transferred to the cobalt(II) amide Co{N(SiMe3)2}2], forming K(18‐c‐6)](HAN){Co(N′′)2}3]; magnetic measurements on this compound reveal an S=4 spin system with strong cobalt–ligand antiferromagnetic exchange and J≈?290 cm?1 (?2 J formalism). In contrast, the CoII centres in the unreduced analogue (HAN){Co(N′′)2}3] are weakly coupled (J≈?4.4 cm?1). The finding that HAN].? can be synthesized as a stable salt and transferred to cobalt introduces potential new routes to magnetic materials based on strongly coupled, triangular HAN building blocks. |
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Keywords: | cobalt hexaazatrinaphthylene magnetism non-innocent ligands radicals |
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