Reduction of hexaazatrinaphthylenes by divalent lanthanocenes leads to ligand-based multiconfigurational properties
Siobhan R Temple1, Jinkui Tang2, Graham J Tizzard3
1Department of Chemistry, School of Life Sciences, University of Sussex, Brighton BN1 9QG, UK. r.layfield@sussex.ac.uk.
Abstract:
Reduction of hexaazatrinaphthylene (HAN) and its hexamethyl derivative with [Cp*2Sm(THF)2] or [Cp*2Yb(OEt2)] produces [(Cp*2Ln)3(R6HAN)] (Ln = Sm, Yb; R = H, Me), where the heterocyclic ligand forms as a trianion. The magnetism and electronic structure of these compounds reflect unusual multiconfigurational character within the reduced ligand but not the lanthanide ions.
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