A new family of sterically demanding N2N' heteroscorpionate pro-ligands (HC(tBu2pz)2SiMe2N(H)R (R = iPr, tBu, Ph, Xyl)) has been prepared via a straightforward modular synthetic route. An extensive study into the synthesis and characterisation of lithium, magnesium, calcium and zinc complexes supported by both 3,5-tBu and 3,5-Me substituted N2N' ligand families has been conducted. Attempted deprotonation of the pro-ligands with nBuLi afforded the corresponding lithium salts Li{HC(tBu2pz)2SiMe2NR} (R = iPr (1), tBu (2), Ph (3) and Xyl (4)) but air- and thermal-sensitivity limited the yields of these potentially useful precursors; only the sterically encumbered ligand system allowed clean reactivity.
View Article and Find Full Text PDFThe reaction of bis(3,5-dimethylpyrazolyl)methylphenol N(2)O(Ar)H (1) with NaH in THF formed dimeric [Na(kappa(2)-N(2)O(Ar))(THF)](2) (2), which contains a kappa(2)(N,O)-bound bidentate N(2)O(Ar) ligand. The reaction of 1 with Mg(n)Bu(2) gave the four-coordinate monomeric butyl compound Mg(N(2)O(Ar))(n)Bu (3), whereas with (n)BuMgCl, a mixture of products was formed, including the six-coordinate homoleptic species Mg(N(2)O(Ar))(2) (4). The reaction of [Na(kappa(2)-N(2)O(Ar))(THF)](2) with (n)BuMgCl also gave 3, as did the redistribution reaction of Mg(n)Bu(2) with 4.
View Article and Find Full Text PDF