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- W2034642810 abstract "Reduction of the tetravalent complex [{2,5-[(C4H3N)CPh2]2[C4H2N(Me)]}ThCl2 (THF)]·THF (2) of the tripyrrolide dianion 2,5-[(C4H3N)CPh2]2C4H2N(Me) afforded different products depending on the reaction conditions. In every case, the reaction proceeded via the initial formation of a reduced species, as indicated by the very rapid formation of a dark red color followed by slow and complete discoloration. In the case of the reduction in toluene, the complexes ({2,5-[(C4H3N)CPh2]2[C4H2N]}2Th[K(toluene)]2)·1.5(toluene) (3a) and {2,5-[(C4H3N)CPh2]2[C4H2N]}2Th[K(DME)]2 (3b) were obtained, depending on the crystallization solvent (toluene versus DME). In both cases, the products arose from a loss of the methyl group attached to the central pyrrole ring N atom. When the reduction was carried out in DME as a solvent, the complex {[{2,5-[(C4H3N)CPh2]2[C4H2N(Me)]}Th(OMe)]2(m-OC2H4OMe)2}· 0.75(hexane) (5) was isolated. This species is derived from two different pathways of C−O cleavage of the DME solvent. Reduction of {2,5-[(C4H3N)CPh2]2[C4H2N(Me)]}ThCl{(C4H3N)CPh2[C4H3N(Me)]} (6), containing both the monoalkylated tripyrrolide and dipyrrolide ligands, afforded instead pyrrolide ring opening and formation of [({2,5-[(C4H3N)CPh2]2[C4H2N(Me)]}Th[(C4H3N)CPh2(CCHCHCHNMe)])2(m-K)][K(DME)4]·2(hexane) (7)." @default.
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- W2034642810 date "2006-07-01" @default.
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- W2034642810 title "Ring Opening and C−O and C−N Bond Cleavage by Transient Reduced Thorium Species" @default.
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- W2034642810 doi "https://doi.org/10.1021/om060454q" @default.
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