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- W1985224946 abstract "New titanium(IV) complexes of the chelating ligand N,N‘-bis(3,5-dimethylphenyl)-phenanthrene-9,10-diamide (pada2-) are described. Metalation of padaH2 with TiCl4 in the presence of base afforded the six-coordinate pyridine adduct (pada)TiCl2(py)2 (1), which was used as a starting point for all further complexes presented in this work. Metathesis of 1 with LiN(SiMe3)2 afforded the four-coordinate complex (pada)TiCl[N(SiMe3)2] (2), free of coordinating pyridine. Further elaboration of 2 with MeLi, PhLi, and PhCH2MgCl provided the mixed alkyl−amido species (pada)TiR[N(SiMe3)2] (3a, R = Me; 3b, R = CH2Ph; 3c, R = Ph), which are all stable in the solid state and in solution. Dichloride 1 reacts directly with 2 equiv of PhCH2MgCl to give the five-coordinate complex (pada)Ti(CH2Ph)2(py) (4). The corresponding dimethyl- and diphenyltitanium complexes could not be isolated; however, generation of these species followed by in situ reaction with tBuNH2 afforded the new titanium imido complex (pada)Ti(NtBu)(py)2 (6). The aryl imido derivative (pada)Ti[N(2,6-C6H3Me2)](py)2 (7) was prepared by transimination of 6 with 2,6-dimethylaniline. Imido complex 6 also reacted with benzaldehyde to give the organic metathesis product benzadimine; however, more crowded ketone and imine substrates were unreactive. Prolonged heating of 6 in the absence of reactive substrates led to irreversible dimerization, forming [(pada)Ti(py)(μ-NtBu)]2 (8)." @default.
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- W1985224946 date "2007-09-28" @default.
- W1985224946 modified "2023-10-16" @default.
- W1985224946 title "Imido and Organometallic-Amido Titanium(IV) Complexes of a Chelating Phenanthrenediamide Ligand" @default.
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- W1985224946 doi "https://doi.org/10.1021/om0701219" @default.
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