Laboratoire Hétéroéléments et Coordination, CNRS, École Polytechnique, Route de Saclay, 91128 Palaiseau (France) http://www.dcph.polytechnique.fr.
Angew Chem Int Ed Engl. 2014 Jan 27;53(5):1368-72. doi: 10.1002/anie.201309222. Epub 2013 Dec 16.
The oxidation of a Ni(II) complex bearing a tetradentate phosphasalen ligand, which differs from salen by the presence of an iminophosphorane (PN) in place of an imine unit, was easily achieved by addition of a silver salt. The site of this oxidation was investigated with a combination of techniques (NMR, EPR, UV/Vis spectroscopy, X-ray diffraction, magnetic measurements) as well as DFT calculations. All data are in agreement with a high-valent Ni(III) center concentrating the spin density. This markedly differs from precedents in the salen series for which oxidation on the metal was only observed at low temperature or in the presence of additional ligands or anions. Therefore, thanks to the good electron-donating properties of the phosphasalen ligand, Ni(Psalen) represents a rare example of a tetracoordinated high-valent nickel complex in presence of a phenoxide ligand.
一个含有四齿膦亚胺配体的 Ni(II) 配合物的氧化很容易通过添加银盐来实现,该配体与 salen 的不同之处在于亚胺单元被亚磷酰胺(PN)取代。通过结合使用各种技术(NMR、EPR、UV/Vis 光谱、X 射线衍射、磁测量)和 DFT 计算,研究了该氧化的位置。所有数据均与高价 Ni(III) 中心集中自旋密度的结果一致。这与 salen 系列中的先例明显不同,在 salen 系列中,只有在低温下或存在额外配体或阴离子时,金属上的氧化才会发生。因此,由于膦亚胺配体的良好供电子性质,[Ni(Psalen)]+在酚氧配体存在的情况下代表了一个罕见的四配位高价镍配合物的例子。