| Literature DB >> 24281814 |
Amélie Kochem1, Gisèle Gellon, Nicolas Leconte, Benoit Baptiste, Christian Philouze, Olivier Jarjayes, Maylis Orio, Fabrice Thomas.
Abstract
Two anilinosalen and a mixed phenol-anilinosalen ligands involving sterically hindered anilines moieties were synthesized. Their nickel(II) complexes 1, 2, and 3 were prepared and characterized. They could be readily one-electron oxidized (E(1/2)=-0.30, -0.26 and 0.10 V vs. Fc(+)/Fc, respectively) into anilinyl radicals species [1](+), [2](+), and [3](+), respectively. The radical complexes are extremely stable and were isolated as single crystals. X-ray crystallographic structures reveal that the changes in bond length resulting from oxidation do not exceed 0.02 Å within the ligand framework in the symmetrical [1](+) and [2](+). No quinoid bond pattern was present. In contrast, larger structural rearrangements were evidenced for the unsymmetrical [3](+), with shortening of one C(ortho)-C(meta) bond. Radical species [1](+) and [2](+) exhibit a strong absorption band at around 6000 cm(-1) (class III mixed valence compounds). This band is significantly less intense than [3](+), consistent with a rather localized anilinyl radical character, and thus a classification of this species as class II mixed-valence compound. Magnetic and electronic properties, as well as structural parameters, have been computed by DFT methods.Entities:
Keywords: X-ray diffraction; aminyl; aniline; ligands; nickel; radicals
Mesh:
Substances:
Year: 2013 PMID: 24281814 DOI: 10.1002/chem.201303228
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236