Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1302516 | Inorganic Chemistry Communications | 2007 | 4 Pages |
2-Hydroxy-5-methylazobenzene (HO–C6H3-p-Me-o-NN–C6H5, 1) reacts with SiCl4 in the presence of triethylamine to yield the [4+4]-coordinate silicon complex 2 [Si(O–C6H3-p-Me-o-NN–C6H5)4]. Its molecular structure has been determined by X-ray crystallography, and 2 represents the first structurally characterized Si-complex bearing o-diazophenoxy ligands. 29Si NMR data suggest that the capped tetrahedral coordination sphere of the Si-atom is retained in solution. Even the difluorocompound 3 [F2Si(O–C6H3-p-Me-o-NN–C6H5)2] still exhibits a tetracoordinate Si-atom, whereas 4 [F2B(O–C6H3-p-Me-o-NN–C6H5)], the byproduct of the formation of 3 from 2, bears a bidentate chelating o-phenyldiazo-p-methylphenoxy ligand.
Graphical abstract2-Hydroxy-4-methylazobenzene (HO–C6H3-p-Me-o-NN–C6H5, 1) reacts with SiCl4 to yield the [4+4]-coordinate silicon complex 2 [Si(O–C6H3-p-Me-o-NN–C6H5)4]. Compound 2 represents the first structurally characterized Si-complex bearing o-diazophenoxy ligands. Its X-ray structure and 29Si NMR data indicate a capped tetrahedral coordination sphere of the Si-atom.Figure optionsDownload full-size imageDownload as PowerPoint slide