Here we have explored the ability of Schiff bases to act as electron reservoirs and to enable the multielectron reduction of small molecules by lanthanide complexes.We report the reductive chemistry of the Ln_((III))c...Here we have explored the ability of Schiff bases to act as electron reservoirs and to enable the multielectron reduction of small molecules by lanthanide complexes.We report the reductive chemistry of the Ln_((III))complexes of the tripodal heptadentate Schiff base H_(3)trensal(2,2’,2’’-tris(salicylideneimino)triethylamine),[Ln_(III)(trensal)],1-Ln(Ln=Sm,Nd,Eu).We show that the reduction of the[Eu^(III)(trensal)]complex leads to the first example of a Eu^((II))Schiff base complex[{K(μ-THF)(THF)_(2)}_(2){EuII(trensal)}_(2)],3-Eu.In contrast the one-and two-electron reduction of the[NdIII(trensal)]and[SmIII(trensal)]leads to the intermolecular reductive coupling of the imino groups of the trensal ligand and to the formation of one and two C-C bonds leaving the metal center in the+3 oxidation state.The resulting one-and two electron reduced complexes[{K(THF)_(3)}_(2)Ln_(2)(bis-trensal)],2-Ln,and[{K(THF)_(3)}_(2){K(THF)}_(2)Ln_(2)(cyclo-trensal)],4-Ln(Ln=Sm,Nd)are able to effect the reductive disproportionation of carbon dioxide by transferring the electrons stored in the C-C bonds to CO_(2)to selectively afford carbonate and CO.The selectivity of the reaction contrasts with the formation of multiple CO_(2)reduction products previously reported for a U_((IV))-trensal system.展开更多
基金support from the Swiss National Science Foundation grant number 178793the Ecole Polytechnique Fédérale de Lausanne(EPFL).
文摘Here we have explored the ability of Schiff bases to act as electron reservoirs and to enable the multielectron reduction of small molecules by lanthanide complexes.We report the reductive chemistry of the Ln_((III))complexes of the tripodal heptadentate Schiff base H_(3)trensal(2,2’,2’’-tris(salicylideneimino)triethylamine),[Ln_(III)(trensal)],1-Ln(Ln=Sm,Nd,Eu).We show that the reduction of the[Eu^(III)(trensal)]complex leads to the first example of a Eu^((II))Schiff base complex[{K(μ-THF)(THF)_(2)}_(2){EuII(trensal)}_(2)],3-Eu.In contrast the one-and two-electron reduction of the[NdIII(trensal)]and[SmIII(trensal)]leads to the intermolecular reductive coupling of the imino groups of the trensal ligand and to the formation of one and two C-C bonds leaving the metal center in the+3 oxidation state.The resulting one-and two electron reduced complexes[{K(THF)_(3)}_(2)Ln_(2)(bis-trensal)],2-Ln,and[{K(THF)_(3)}_(2){K(THF)}_(2)Ln_(2)(cyclo-trensal)],4-Ln(Ln=Sm,Nd)are able to effect the reductive disproportionation of carbon dioxide by transferring the electrons stored in the C-C bonds to CO_(2)to selectively afford carbonate and CO.The selectivity of the reaction contrasts with the formation of multiple CO_(2)reduction products previously reported for a U_((IV))-trensal system.
