Exploring the structure and redox activity of hexacoordinate bis(bipyridyl)silicon(IV) complexes

• Published in: Polyhedron Vol. 94; pp. 52 - 58
• Main Authors: Maguylo, Christina, Chukwu, Chika, Aun, Mya, Blake Monroe, T., Ceccarelli, Christopher, Jones, Daniel S., Merkert, Jon W., Donovan-Merkert, Bernadette T., Schmedake, Thomas A.
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 07-07-2015
• Subjects: Bipyridine; Coordination chemistry; Crystallography; Electrochemistry; Hexacoordinate silicon; Hexacoordinate silicon; Electrochemistry; Crystallography; Bipyridine; Coordination chemistry
• ISSN: 0277-5387
• DOI: 10.1016/j.poly.2015.04.001

The structures of a series of hexacoordinate bis(bipyridyl)silicon(IV) complexes are reported. The hexafluorophosphate salts of each complex cation exhibit a reversible, first reduction wave around −1V (versus Fc+/Fc) in acetonitrile, nearly independent of the alkoxide or diolate substituent. The complexes with bidentate diolate ligands possess multiple, reversible reduction waves. [Display omitted]
A series of hexacoordinate bis(bipyridyl)silicon(IV) complexes was synthesized by allowing [Si(bpy)2I2]I2 to react with the alcohols or phenols: methanol, ethylene glycol, phenol, 2,2′-biphenol, or 1,2-benzendiol. Crystal structures were obtained for the corresponding complexes: [Si(bpy)2(OMe)2] (I)(I3) (1), [Si(bpy)2(-OCH2CH2O-)]I2 (2), [Si(bpy)2(OPh)2](I3)2 (3), [Si(bpy)2(bph)](PF6)2 (4), and [Si(bpy)2(cat)](PF6)2 (5), (bpy=2,2′-bipyridine, cat=1,2-benzenediolato, bph=2,2′-biphenolato ligand). All five complexes exist as distorted octahedral dications with readily exchangeable counterions. The hexafluorophosphate salts of each complex cation exhibit a reversible, first reduction wave around −1V (versus Fc+/Fc) in acetonitrile, nearly independent of the alkoxide or diolate substituent. This is consistent with DFT calculations indicating a LUMO localized on the bipyridyl ligands. The complexes with bidentate diolate ligands possess multiple reversible reduction waves.