The first divalent ytterbium complex supported by a diaminobis(phenolate) ligand, YbL(THF)
2·0.5C
7H
8 (
1; THF =tetrahydrofuran), was synthesized in good yield by the amine elimination reaction of Yb[N(SiMe
3)
2]
2(THF)
2 with H
2L(L = [Me
2NCH
2CH
2N(CH
2-2-OC
6H
2-3,5-Bu
t2)
2]) in a 1:1 molar ratio. X-ray structural determination shows complex
1 to be a THF-solvated monomer, which adopts a distorted octahedral coordination geometry around the Yb atom.Complex
1 can react with PhNCO and PhC
CH, as a single electron-transfer reagent, to give the correspondingreduction coupling product [(YbLOCNPh)(THF)]
2·4THF (
2) and the alkynide complex YbLC
CPh(DME) (
3; DME= 1,2-dimethoxyethane). Complexes
2 and
3 have been characterized by X-ray crystal structural analysis. Incomplex
2, the dianionic oxamide ligand resulting from the reductive coupling of two phenyl isocyanate moleculescoordinates to two Yb atoms in a
,
4 fashion. Complex
3 has a monomeric structure with a Yb-C(terminalphenylacetynide) bond length of 2.374(3) Å. Complex
1 is also a highly efficient catalyst for ring-opening polymerizationof
-caprolactone.