Ns. Hosmane et al., SANDWICHED METALLACARBORANES OF F-BLOCK ELEMENTS, Phosphorus, sulfur and silicon and the related elements, 93(1-4), 1994, pp. 253-256
The dilithium complexed ''carbons adjacent'' nido-carborane anions of
the type [2-(SiMe(3))-3-(R)-2,3-C2B4H4](2-) [R = SiMe(3), Me, H], as w
ell as the disodium and dilithium complexed ''carbons apart'' nido-car
borane anions [2-(SiMe(3))-4-(R)-2,4-C2B4H4](2-) [R = SiMe(3), Me] hav
e exhibited different reactivity patterns toward various lanthanide ha
lides, depending upon the solvents used in the reactions and the natur
e of the group 1 metal. Both the tetrahydofuran (THF) and N, N, N, N-t
etramethylethylenediamine (TMEDA)-solvated closo-dilithiacarboranes ha
ve been found to be important synthons in the production of novel meta
llacarboranes of f-block elements. Several unprecedented examples of l
anthanide-carborane complexes have been synthesized, their structures
determined and reactivity studied.