| Autor: |
Goodwin CA; School of Chemistry, The University of Manchester , Oxford Road, Manchester M13 9PL, U.K., Chilton NF; School of Chemistry, The University of Manchester , Oxford Road, Manchester M13 9PL, U.K., Vettese GF; School of Chemistry, The University of Manchester , Oxford Road, Manchester M13 9PL, U.K., Moreno Pineda E; School of Chemistry, The University of Manchester , Oxford Road, Manchester M13 9PL, U.K., Crowe IF; Photon Science Institute and School of Electrical and Electronic Engineering, The University of Manchester , Oxford Road, Manchester M13 9PL, U.K., Ziller JW; Department of Chemistry, University of California , Irvine, California 92697-2025, United States., Winpenny RE; School of Chemistry, The University of Manchester , Oxford Road, Manchester M13 9PL, U.K., Evans WJ; Department of Chemistry, University of California , Irvine, California 92697-2025, United States., Mills DP; School of Chemistry, The University of Manchester , Oxford Road, Manchester M13 9PL, U.K. |
| Abstrakt: |
Following our report of the first near-linear lanthanide (Ln) complex, [Sm(N †† ) 2 ] (1), herein we present the synthesis of [Ln(N †† ) 2 ] [N †† = {N(Si i Pr 3 ) 2 }; Ln = Eu (2), Tm (3), Yb (4)], thus achieving approximate uniaxial geometries for a series of "traditional" Ln II ions. Experimental evidence, together with calculations performed on a model of 4, indicates that dispersion forces are important for stabilization of the near-linear geometries of 1-4. The isolation of 3 under a dinitrogen atmosphere is noteworthy, given that "[Tm(N″)(μ-N″)] 2 " (N″ = {N(SiMe 3 ) 2 }) has not previously been structurally authenticated and reacts rapidly with N 2 (g) to give [{Tm(N″) 2 } 2 (μ-η 2 :η 2 -N 2 )]. Complexes 1-4 have been characterized as appropriate by single-crystal X-ray diffraction, magnetic measurements, electrochemistry, multinuclear NMR, electron paramagnetic resonance (EPR), and electronic spectroscopy, along with computational methods for 3 and 4. The remarkable geometries of monomeric 1-4 lead to interesting physical properties, which complement and contrast with comparatively well understood dimeric [Ln(N″)(μ-N″)] 2 complexes. EPR spectroscopy of 3 shows that the near-linear geometry stabilizes m J states with oblate spheroid electron density distributions, validating our previous suggestions. Cyclic voltammetry experiments carried out on 1-4 did not yield Ln II reduction potentials, so a reactivity study of 1 was performed with selected substrates in order to benchmark the Sm III → Sm II couple. The separate reactions of 1 with 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO), azobenzene, and benzophenone gave crystals of [Sm(N †† ) 2 (TEMPO)] (5), [Sm(N †† ) 2 (N 2 Ph 2 )] (6), and [Sm(N †† ){μ-OPhC(C 6 H 5 )CPh 2 O-κO,O'}] 2 (7), respectively. The isolation of 5-7 shows that the Sm II center in 1 is still accessible despite having two bulky N †† moieties and that the N-donor atoms are able to deviate further from linearity or ligand scrambling occurs in order to accommodate another ligand in the Sm III coordination spheres of the products. |
