No abstract

Three new anilido-oxazolines, ortho-C(6)H(4)(NHAr')(4,4-dimethyl-2-oxazoline) [Ar'=2,4,6-trimethylphenyl, HNPh(TriMe)Oxa (1); 2,6-diisopropylphenyl, HNPh(DiiPr)Oxa (2); 2-methoxyphenyl, HNPh(OMe)Oxa (3)], have been prepared. Reactions of 1 or 2 with one molar equivalent of ZnEt(2) in tetrahydrofuran or hexane solution give the zinc ethyl complexes (NPh(TriMe)Oxa)ZnEt (4) and (NPh(DiiPr)Oxa)ZnEt (5). The dinuclear zinc benzyloxide complexes, [(NAr'Oxa)Zn(mu-OBn)](2), [Ar'=2,4,6-trimethylphenyl, (6); 2-methoxyphenyl, (7)], were synthesized by the reaction of 4 with one molar equivalent of benzyl alcohol in tetrahydrofuran solution (for 6) or by treatment of with 3 one molar equivalent of ZnEt(2) in tetrahydrofuran solution followed by the addition of one molar equivalent of benzyl alcohol (for 7). The molecular structures are reported for compounds 6 and 7. Their catalytic activities toward the ring opening polymerization reactions are under investigation.

Three novel indole-based ligand precursors [HIndPh(R), R = methoxy, HIndPh(OMe) (); thiomethoxy, HIndPh(SMe) (); and N,N'-dimethylamino, HIndPh(NMe2) ()] have been synthesized via Sonogashira and cyclization reactions with moderate to high yield. Reactions of these ligand precursors with 0.6 equivalent of Mg(n)Bu2 in THF afforded the magnesium bis-indolyl complexes , respectively. All the ligand precursors and related magnesium complexes have been characterized by NMR spectroscopy and elemental analyses. The molecular structures are reported for compounds and . Under optimized conditions, compound demonstrates efficient catalytic activities towards the ring opening polymerization of l-lactide and ε-caprolactone in the presence of BnOH.

A series of aluminium complexes containing anilido-pyrazolate ligands is described. Reactions of four anilido-pyrazolate ligand precursors, HNPhPz, HNPhTriMePz, HNPhOMePz, or HNPhSMePz [HNPhPz = ortho-C6H4(NH-phenyl)(1-pyrazole); HNPhTriMePz = ortho-C6H4(NH-2,4,6-trimethylphenyl)(1-pyrazole); HNPhOMePz = ortho-C6H4(NH-2-methoxyphenyl)(1-pyrazole); HNPhSMePz = ortho-C6H4(NH-2-methylthiophenyl)(1-pyrazole)], with one molar equivalent of AlMe3 in toluene give the aluminium dimethyl complexes, (NArPz)AlMe2 [Ar = phenyl, (NPhPz)AlMe2 (1); Ar = 2,4,6-trimethylphenyl, (NPhTriMePz)AlMe2 (2); Ar = 2-methoxyphenyl, (NPhOMePz)AlMe2 (3); Ar = 2-methylthiophenyl, (NPhSMePz)AlMe2 (4)], respectively. The molecular structures are reported for compounds 1 and 3. Their catalytic activities toward the ring opening polymerisation reaction of -caprolactone in the presence of BnOH are also under investigation.