Titanium and zirconium complexes of the N,N'-bis(2,6-diisopropylphenyl)-1,4-diaza-butadiene ligand: syntheses, structures and uses in catalytic hydrosilylation reactions.

We report here a number of dianionic 1,4-diaza-1,3-butadiene complexes of titanium and zirconium synthesised by a salt metathesis reaction. The reaction of either CpTiCl3 or Cp2TiCl2 with the dilithium salt of N,N'-bis(2,6-diisopropylphenyl)-1,4-diaza-1,3-butadiene [; abbreviated (Dipp)2DADLi2] afforded the mono-cyclopentadienyl titanium complex [η(5)-CpTi((Dipp)2DAD)Cl] () bearing a dianionic ene-diamide ligand, while the analogous reaction of zirconocene dichloride (Cp2ZrCl2) with the dilithium salt gave the bis-cyclopentadienyl zirconium complex [Cp2Zr{(Dipp)2DAD}] (). The metal dichloride complexes [Ti((Dipp)2DAD)Cl2] () and [{(Dipp)2DADZrCl(μ-Cl)}2(κ(3)-Cl)(Li)(OEt2)2] () were obtained by the reaction of and anhydrous metal tetrachloride in a 1 : 1 molar ratio in diethyl ether at room temperature. Meanwhile, the homoleptic titanium complex [Ti{((Dipp)2DAD)}2] () was isolated in good yield by the treatment of with TiCl4 in a 1 : 2 molar ratio in diethyl ether. The complexes and were further reacted with neosilyl lithium to afford mono- and bis-alkyl complexes of titanium [η(5)-CpTi{(Dipp)2DAD}(CH2SiMe3)] () and zirconium [Zr{(Dipp)2DAD}(CH2SiMe3)2] () respectively. Molecular structures of the complexes , , and in the solid states were confirmed by single crystal X-ray diffraction analysis. The solid state structures of all the complexes reveal that the metal ions are chelated through the amido-nitrogen atoms and the olefinic carbons of the [(Dipp)2DAD](2-) moiety, satisfying the σ(2),π coordination mode. Compound was used as a catalyst for the intermolecular hydrosilylation reaction of a number of olefins, and moderate activity of catalyst was observed.