Reactions of Co2(CO)8 and of Co2(CO)6L (L=3-pentyn-1-ol, 1,4-butyn-diol or 2-methyl-3-buthyn-2-ol) with 2(diphenylphosphino)ethyl-trietoxysilane and tris(hydroxymethyl)phosphine for applications to new sol-gel materials

The complex Co2(CO)6[l-g2-(H3CC„CCH2CH2OH)] (1) with the ligand 3-pentyn-1-ol (pol) has been synthesized following established procedures. Its structure has been determined by X-ray analysis. The complex Co2(CO)6(mbo) (mbo = 2-methyl-3-butyn-2-ol, HC„CC(CH3)2OH), (3), along with the already known Co2(CO)6(bud) (bud = 1,4-butyn-diol, HOCH2C„CCH2OH) (2), and Co2(CO)8 were reacted with 2(diphenylphosphino) ethyl-triethoxysilane [Ph2PCH2CH2Si(OCH2CH3)3] (dpts) and tris(hydroxymethyl)phosphine [P(CH2OH)3] (thp). With dpts, mono- and di-substituted complexes were obtained: these were characterized by analytical and spectroscopic techniques. The structures of Co2(CO)6(dpts)2 (5) and of Co2(CO)4- (pol)(dpts)2 (8) have been determined by X-ray analysis. Complex (1) was reacted with 3-(triethoxysilyl)propyl isocyanate [(H3CCH2O)3Si(CH2)3NCO] (tsi): the new complex Co2(CO)6[H3CC„CCH2CH2OC(@O)NH(CH2)3Si(OCH2CH3)3] (9) was obtained and spectroscopically characterized. The complex has also been reacted with tetraethyl orthosilicate (teos); a new inorganic–organometallic material was obtained. Complex (5) has been grafted on the mesoporous material SBA-15. The hybrid inorganic–organometallic materials obtained have been characterized by inductively coupled plasma-mass spectrometry (ICP-MS), infrared spectroscopy (FT-IR) under vacuum conditions, X-ray diffraction (XRD) and scanning electron microscopy coupled to EDS probe (SEM–EDS).