کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1334387 1500245 2015 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Exploring the structure and redox activity of hexacoordinate bis(bipyridyl)silicon(IV) complexes
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Exploring the structure and redox activity of hexacoordinate bis(bipyridyl)silicon(IV) complexes
چکیده انگلیسی

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 −1 V (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.

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 −1 V (versus Fc+/Fc) in acetonitrile, nearly independent of the alkoxide or diolate substituent. The complexes with bidentate diolate ligands possess multiple, reversible reduction waves.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Polyhedron - Volume 94, 7 July 2015, Pages 52–58
نویسندگان
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