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Mauricio Lanznaster

Researcher at Federal Fluminense University

Publications -  46
Citations -  1181

Mauricio Lanznaster is an academic researcher from Federal Fluminense University. The author has contributed to research in topics: Ligand & Ascorbic acid. The author has an hindex of 18, co-authored 46 publications receiving 1022 citations. Previous affiliations of Mauricio Lanznaster include Wayne State University & Universidade Federal de Santa Catarina.

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Journal ArticleDOI

An unprecedented Fe(III)(mu-OH)Zn(II) complex that mimics the structural and functional properties of purple acid phosphatases.

TL;DR: It is demonstrated that the μ-hydroxo group in the {FeIII(μ-OH)(μ-ROPO3)ZnII} intermediate is unable to hydrolyze the monoester 2,4-dinitrophenylphosphate (DNPP), which suggests that theμ-hydroxyo group is a significantly poorer nucleophile than the terminally FeIII-bound OH- group.
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New FeIIIZnII Complex Containing a Single Terminal Fe−Ophenolate Bond as a Structural and Functional Model for the Active Site of Red Kidney Bean Purple Acid Phosphatase

TL;DR: Solution studies of 1 indicate that a pH-induced change of the bridging acetate occurs, and the formation of an active [(OH)Fe(III)Zn(II)(OH(2))] species as a highly efficient catalyst under weakly acidic conditions for phosphate diesters hydrolysis is proposed.
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Synthesis, Structure, Properties, and Phosphatase-Like Activity of the First Heterodinuclear FeIIIMnII Complex with the Unsymmetric Ligand H2BPBPMP as a Model for the PAP in Sweet Potato

TL;DR: The new heterodinuclear mixed valence complex [Fe(III)Mn(II)(BPBPMP)(OAc)(2)]ClO(4) (1) with the unsymmetrical N(5)O(2) donor ligand 2-bis[((2-pyridylmethyl)-aminomethyl)-6-(2-hydroxybenzyl)(2- pyrIDylmethyl))-aminometHyl]-4
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Influence of ligand rigidity and ring substitution on the structural and electronic behavior of trivalent iron and gallium complexes with asymmetric tridentate ligands.

TL;DR: Monometallic species with d5 high-spin iron and d10 gallium were synthesized and characterized to assess the influence of the ligand rigidity and the presence of tertiary butyl-substituted phenol rings on their steric, electronic, and redox behavior.