Strong Exchange Coupling in a Trimetallic Radical-Bridged Cobalt(II)-Hexaazatrinaphthalene Complex

Research output: Research - peer-reviewArticle

  • Authors:
  • Jani O. Moilanen
  • Nicholas Chilton
  • Benjamin M. Day
  • Thomas Pugh
  • Richard A. Layfield


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.

Bibliographical metadata

Original languageEnglish
Pages (from-to)5521–5525
JournalAngewandte Chemie (International Edition)
Issue number18
Early online date21 Mar 2016
StatePublished - 10 Apr 2016

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