Sm. Stuczynski et al., THE USE OF PHOSPHINE CHALCOGENIDES IN THE PREPARATION OF COBALT CHALCOGENIDES, Journal of organometallic chemistry, 449(1-2), 1993, pp. 167-172
Dicobalt octacarbonyl reacts with TePnBu3, SePnBu3 or SPnBu3 to give s
olid state cobalt telluride, cobalt selenide and cobalt sulfide, respe
ctively. In each case a cluster compound of the form Co6E8 (PnBu3)6 ca
n be isolated from the reaction of the phosphine chalcogenide with cob
alt carbonyl, and subsequently carried on to the solid state product.
In this sense the Co6E8 clusters are intermediates in the molecules-to
-solids processes. In the case of Se, another Co/Se cluster can be iso
lated: Co4Se2(CO)6(PnBu3)4. This complex also fits into the molecules-
to-solids pathway inasmuch as it arises from Co2(CO)8 and SePnBU3, and
it is converted to the Co6Se8 cluster when treated with phosphine sel
enide. These results show that molecules-to-solids pathways originally
uncovered in studying reactions of TePEt3 can be extended to other tr
ialkylphosphines and other chalcogens.