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- W2061442129 abstract "The tris-benzimidazolium cage LH(3)(3+), in MeCN solution, in the presence of OH(-), forms with Cu(I) and Ag(I) ions complexes of formula [M(I)(LH)](2+), in which each metal is linearly coordinated by two carbenes and one imidazolium N-H fragment remains intact. To achieve two-coordination, the two N-heterocyclic moieties of the cage make a saloon-door type motion, with a conformationally costless rotation of ca. 30° each. The two [M(I)(LH)](2+) complexes show high thermodynamic stability and are inert with respect to metal substitution, due to the mechanical constraints imposed by the ligating framework. Complexation with Cu(I) and Ag(I) with the reference unidentate carbene ligand Q, derived from the benzimidazolium precursor QH(+), was studied for comparison. Both metals in MeCN form 1:1 and 1:2 complexes with the carbene ligand Q according to two stepwise equilibria. Q complexes of both metals are labile with respect to metal substitution and those of Ag(I) are more stable than those of Cu(I). A significant cooperative effect has been observed with the formation of the [Ag(I)Q(2)](+) complex." @default.
- W2061442129 created "2016-06-24" @default.
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- W2061442129 date "2011-01-01" @default.
- W2061442129 modified "2023-10-14" @default.
- W2061442129 title "The solution stability of copper(i) and silver(i) complexes with N-heterocyclic carbenes" @default.
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- W2061442129 doi "https://doi.org/10.1039/c1dt10894h" @default.
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