Abstract

A series of oxo-vanadium(IV) complexes: Tp ∗VO(pzH ∗)(CH 3COO) ( 1), Tp ∗VO(pzH ∗)(CCl 3COO) ( 2), Tp ∗VO(pzH ∗)(C 6H 5COO) ( 3), Tp ∗VO(pzH ∗)( m-NO 2–C 6H 4COO)·CH 3CN ( 4) and [Tp ∗VO(pzH ∗)(H 2O)] +[ m-NO 2–C 6H 4–SO 3] −·CH 3OH ( 5) (Tp ∗ = hydrotris(3,5-dimethylpyrazolyl)borate; pzH ∗ = 3,5-dimethylpyrazole) are synthesized in methanol solution under physiological conditions. They are characterized by elemental analysis, IR, UV–Vis and X-ray crystallography. Structural analyses show that the vanadium atoms in complexes 1– 5 are all in a distorted-octahedral environment with the N 4O 2 donor set, and intra- or inter-hydrogen bonding linkages have been also observed in each complex. Bromination reaction activity of the complexes has been evaluated by the method with phenol red as organic substrate in the presence of H 2O 2, Br − and phosphate buffer, indicating that they can be considered as potential functional model vanadium-dependent haloperoxidases. In addition, thermal analysis and quantum chemistry calculations were also performed and discussed in detail.

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