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Updated: Feb 18, 2026

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyltroponeiron
Published on: August 12, 2019
f-Block complexes of a m-terphenyl dithiocarboxylate ligand
Michael A Boreen1, Bernard F Parker2, Stephan Hohloch2
1Department of Chemistry, University of California, Berkeley, California 94720, USA. arnold@berkeley.edu.
Abstract:
Straightforward syntheses are provided for the m-terphenyl dithiocarboxylic acid 2,6-(C6H4-4-tBu)2C6H3CS2H (TerphCS2H, 2) and its lithium and potassium salts, TerphCS2Li(Et2O)2 and TerphCS2K (1·Et2O and 4, respectively). These compounds can be isolated in good yields on multi-gram scales starting from Terph-I without isolating intermediates. Salt metathesis and protonolysis reactions provided access to the homoleptic actinide(iv) complexes (TerphCS2)4An (An = Th (5) and U (6)). Electrochemical and reactivity studies revealed that the dithiocarboxylate ligand is incompatible with U(iii). The homoleptic lanthanum(iii) complex (TerphCS2)3La and its η6-toluene adduct (7 and 7·tol, respectively) were also structurally characterized. Binding of toluene to 7 was shown to displace intramolecular La-Carene close contacts that are facilitated by a distortion from the usual geometry of bound dithiocarboxylate ligands.
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