The thorium bipyridyl
metallocene (Cp3tBu)2Th(bipy)
(1; Cp3tBu = η5-1,2,4-(Me3C)3C5H2) shows a rich reactivity toward a series
of small molecules. For example, complex 1 may act as
a synthon for the (Cp3tBu)2Th(II) fragment as illustrated by its reactivity toward to CuI, hydrazine
derivative (PhNH)2, Ph2
E
2 (E = S, Se), elemental sulfur (S8) and selenium (Se), organic azides, CS2, and isothiocyanates.
Moreover, in the presence of polar multiple bonds, such as those in
ketones Ph2CO and (CH2)5CO, aldehydes p-MePhCHO and p-ClPhCHO, seleno-ketone
(p-MeOPh)2CSe, nitriles PhCN, Ph2CHCN, C6H11CN, and p-(NC)2Ph, and benzoyl cyanide PhCOCN, C–C coupling occurs
to furnish (Cp3tBu)2Th[(bipy)(Ph2CO)] (10), (Cp3tBu)2Th[(bipy)((CH2)5CO)] (11), (Cp3tBu)2Th[(bipy)(p-MePhCHO)] (12), (Cp3tBu)2Th[(bipy)(p-ClPhCHO)] (13), (Cp3tBu)2Th[(bipy){(p-MeOPh)2CSe}] (14), (Cp3tBu)2Th[(bipy)(PhCN)] (16),
(Cp3tBu)2Th[(bipy)(Ph2CHCN)] (17), (Cp3tBu)2Th[(bipy)(C6H11CN)] (18), [(Cp3tBu)2Th]2{μ-(bipy)[p-Ph(CN)2](bipy)} (20), and (Cp3tBu)2Th{(bipy)[PhC(CN)O]}
(21), respectively. Nevertheless, ketazine (PhCHN)2 or benzyl nitrile PhCH2CN forms the dimeric complexes
[(Cp3tBu)Th]2[μ-NC(Ph)(bipy)]2 (15) and (Cp3tBu)2Th[(bipy){C(CHPh)NH}] (19), respectively.
In contrast, C–N bond cleavage and C–C coupling processes
occur upon addition of isonitriles Me3CNC and C6H11NC to 1 to yield the thorium isocyanido
amido complexes (Cp3tBu)2Th[4-(Me3C)bipy](NC) (22) and (Cp3tBu)2Th[4-(C6H11)bipy](NC)
(23), respectively. Furthermore, a single-electron transfer
(SET) process ensues when 1 equiv of CuI is added to 1 to yield the Th(VI) bipyridyl iodide complex (Cp3tBu)2Th(I)(bipy) (3).