f-Block complexes of a m-terphenyl dithiocarboxylate ligand†
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.
- This article is part of the themed collection: Philip Power at 65: an icon of organometallic chemistry