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Seyed Amir Zarei

Researcher at Islamic Azad University

Publications -  31
Citations -  406

Seyed Amir Zarei is an academic researcher from Islamic Azad University. The author has contributed to research in topics: Schiff base & Crystal structure. The author has an hindex of 11, co-authored 31 publications receiving 349 citations. Previous affiliations of Seyed Amir Zarei include University of Tabriz.

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Synthesis, characterization and X-ray crystal structures of copper(II) and nickel(II) complexes with potentially hexadentate Schiff base ligands

TL;DR: In this article, the single-crystal X-ray diffraction of copper(II) and nickel (II) complexes of potentially N2O4 Schiff base ligands 2-({[2-(2-{2]-(1-{ 2-hydroxy-5-[2-phenyl-1-diazenyl]phenyl}methylidene)amino] phenoxy}ethoxy) phenyl]imino}methyl)4-[2phenyl]-methyl)
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The role of structural CH compared with phenolic OH sites on the antioxidant activity of oleuropein and its derivatives as a great non-flavonoid family of the olive components: A DFT study

TL;DR: The experimental results of the previous publications of oleuropein for NO and OH scavenging confirmed the presence of this unique active site in its molecular structure, but 2,2-diphenylpicrylhydrazyl (DPPH) cannot find this non-marginal active site and may not be a determinant assay for all antioxidant comparisons.
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A density functional theory study of the reactivity descriptors and antioxidant behavior of Crocin

TL;DR: In this article, the molecular characteristics of Crocin (digentiobiosyl-8,8′-diapocarotene-8-8′)-8, 8′-oate; C44H64O24), naturally occurring carotenoid pigment compound, such as: the ionization potential (I), electron affinity (A), electronegativity (χ), electrophicility (ω), and hardness have been calculated using Density Functional Theory (DFT) approach with B3LYP/6-31G(d
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Nickel(II) and copper(II) complexes of Schiff base ligands containing N4O2 and N4S2 donors with pyrrole terminal binding groups: Synthesis, characterization, X-ray structures, DFT and electrochemical studies

TL;DR: A series of hexadentate ligands, H2Lm (m = 1−4), [1H-pyrrol-2-ylmethylene]{2]-2-(2-{[1H pyrrol 2-yl methylene]amino}phenoxy)ethoxy]phenyl}amine (H2L1), [ 1H-polycyclic voltammetry indicates that all copper complexes are electrochemically inactive but the nickel complexes with softer thioethers are more easily oxidized than their oxygen analogs as discussed by the authors.
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Synthesis, characterization and structure of nickel(II) complexes of a 16-membered mixed-donor macrocyclic Schiff base ligand, potentially hexadentate, bearing two pendant alcohol functions

TL;DR: In this paper, a template condensation of 2-[3-(2-formylphenoxy)-2-hydroxypropoxy]benzaldehyde and 1,3-diamino-2-propanol has been carried out and IR and UV-Vis spectroscopy, conductance measurements and X-ray determination have been employed to probe the nature of the respective complexes in both solid and solution states.