Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1326039 | Journal of Organometallic Chemistry | 2008 | 8 Pages |
The cyclopalladation of 3,5-bis(diphenylphosphinothioyl)pyridine afforded new κ3S,C,S-pincer palladium complexes with a σ-bond between Pd and 4C of the centered 3,5-pyridinediyl unit. By utilizing the quaternization and complexation ability of the pyridine imine nitrogen (Npy) atom, various new pincer-type complexes, including hetero-binuclear complexes, have been synthesized.
Graphical abstractThe cyclopalladation of 3,5-bis(diphenylphosphinothioyl)pyridine afforded new κ3S,C,S-pincer palladium complexes with a σ-bond between Pd and 4C of the centered 3,5-pyridinediyl unit. By utilizing the quaternization and complexation ability of the pyridine imine nitrogen (Npy) atom, various new pincer-type complexes, including hetero-binuclear complexes, have been synthesized.Figure optionsDownload full-size imageDownload as PowerPoint slide