222527-16-4Relevant articles and documents
η6-coordination of arsenine to titanium, vanadium, and chromium
Elschenbroich, Christoph,Kroker, J?rg,Nowotny, Mathias,Behrendt, Andreas,Metz, Bernhard,Harms, Klaus
, p. 1495 - 1503 (2008/10/08)
By means of metal-ligand vapor co-condensation techniques the homoleptic arsenine sandwich complexes (η6-C5H5As)2Ti (2), (η6-C5H5As)2V (3), and (η6-C5H5As)2Cr (4) have been prepared. 2 is the first example of an unsubstituted group 15 heteroarene sandwich complex which yielded to full structural characterization by X-ray diffraction. The most remarkable feature of the structure of 2 in the crystal is the synperiplanar conformation and the short intramolecular interannular As?As distances which imply secondary bonding. The latter may also contribute to the packing since interannular As?As distances, which fall short of the sum of the van der Waals radii, are detected. The result of a competition experiment, in which benzene and arsenine are offered as ligands to chromium, illustrate the pronounced preference of chromium for arsenine as an η6 ligand. The mixed-ligand complexes (η6-C5H5As)(η6-C 6H6)Cr (6) and (η6-C5H5As)Cr(CO)3 (8) have also been prepared and studied spectroscopically in order to underpin the notion that arsenine, compared to benzene, is the superior η6 ligand. The study is rounded off by an investigation of the redox behavior of 2, 3, 4, and 6 (cyclic voltammetry) and by EPR measurements on 3? and 4?+. The latter confirm the pronounced π-acceptor character of η6-arsenine. This conclusion is based on the increase of the hyperfine coupling constant α(51V) upon going from bis(benzene)vanadium to the arsenine counterpart which is thought to reflect V(dz2) orbital contraction in 3?, caused by a slight increase of positive partial charge on vanadium.
