Oxidative stretching of metal-metal bonds to their limits.
2014
Oxidation of quadruply bonded Cr2(dpa)4 ,M o 2(dpa)4, MoW(dpa)4, and W2(dpa)4 (dpa = 2,2'-dipyridylamido) with 2 equiv of silver(I) triflate or ferrocenium triflate results in the formation of the two- electron-oxidized products (Cr2(dpa)4) 2+ (1), (Mo2(dpa)4) 2+ (2), (MoW- (dpa)4) 2+ (3), and (W2(dpa)4) 2+ (4). Additional two-electron oxidation and oxygen atom transfer by m-chloroperoxybenzoic acid results in the formation of the corresponding metal−oxo compounds (Mo2O(dpa)4) 2+ (5), (WMoO(dpa)4) 2+ (6), and (W2O(dpa)4) 2+ (7), which feature an unusual linear M···MO structure. Crystallographic studies of the two- electron-oxidized products 2, 3, and 4, which have the appropriate number of orbitals and electrons to form metal−metal triple bonds, show bond distances much longer (by >0.5 A) than those in established triply bonded compounds, but these compounds are nonetheless diamagnetic. In contrast, the Cr−Cr bond is completely severed in 1, and the resulting two isolated Cr 3+ magnetic centers couple antiferromagnetically with J/kB= −108(3) K (−75(2) cm −1 ), as determined by modeling of the temperature dependence of the magnetic susceptibility. Density functional theory (DFT) and multiconfigurational methods (CASSCF/CASPT2) provide support for "stretched" and weak metal−metal triple bonds in 2, 3, and 4. The metal−metal distances in the metal−oxo compounds 5, 6, and 7 are elongated beyond the single-bond covalent radii of the metal atoms. DFT and CASSCF/CASPT2 calculations suggest that the metal atoms have minimal interaction; the electronic structure of these complexes is used to rationalize their multielectron redox reactivity.
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