A series of Ta(V)
t
Bu-imido/N-alkoxy carboxamide
complexes, TaCl2(N
t
Bu)(pyridine)(edpa)
(1), TaCl(N
t
Bu)(edpa)2 (2), Ta(N
t
Bu)(edpa)3 (3), TaCl2(N
t
Bu)(pyridine)(mdpa) (4), and Ta(N
t
Bu)(mdpa)3 (5), were successfully
synthesized by metathesis reactions
between Ta(N
t
Bu)Cl3(py)2 and several equivalents of Na(edpa) (edpaH = N-ethoxy-2,2-dimethylpropanamide) and Na(mdpa) (mdpaH = N-methoxy-2,2-dimethylpropanamide). Furthermore, complexes 3 and 5 were simply transformed to new dimeric structures
[Ta(μ2–O)(edpa)3]2 (6) and [Ta(μ2–O)(mdpa)3]2 (7) with the elimination of the N
t
Bu imido group by air exposure. Compounds 1–7 were characterized by 1H and 13C nuclear magnetic resonance spectroscopy, Fourier
transform infrared spectroscopy, elemental analysis, thermogravimetric
analysis (TGA), and single-crystal X-ray diffraction. Single-crystal
X-ray diffraction analysis revealed that complexes 3 and 5 have a distorted pentagonal bipyramidal geometry around
the central Ta atom, with three monoanionic bidentate N-alkoxy carboxamide ligands and one
t
Bu imido ligand saturating the coordination of tantalum ions. TGA
revealed that complexes 3 and 5 had superior
thermal characteristics and stability. These complexes could potentially
be applied as precursors for tantalum oxide thin films.