Hydrazones as analytical reagents: a review
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Cited by (184)
Preparation, investigation, DFT, pH-metric and cyclic voltammetry of Cr(III), Fe(III), Co(II), Ni(II) and Cu(II) complexes derived from 2-(2-((2Z,3Z)-3-(hydroxyimino) butan-2-ylidene) hydrazineyl)-2-oxo-N-(pyridin-2-yl) acetamide (H<inf>3</inf>BYPA) and evaluation of their biological activity
2023, Journal of Molecular StructureCitation Excerpt :They can be described by the following generic structure R2CNNR2. Because of their many uses in biological, pharmacological, analytical, catalytic, and industrial sectors, hydrazone ligands and their metal complexes were widely employed by many researchers [1–5]. They play significant roles in treatment of various disorders.
Synthesis, thermodynamic properties and Hirshfeld surface analysis of 2-[(4-methyl-benzoyl)-hydrazone]-propionic acid
2022, Journal of Molecular StructureAn insight into the coordination specificity of polyaromatic hydrocarbons (PAHs) grafted hydrazones towards rhodium(III)
2021, PolyhedronCitation Excerpt :Additionally, the >CN− moiety has the ability to exhibit configurational isomerism and the presence of an acidic amine NH proton is also instrumental for their aptitude to display a variety of metal-hydrazone bonding interactions [1,2]. The coordination diversity of hydrazones have been extensively explored and further deliberations are still in progress [3–6]. Current reports reveal that hydrazones, upon coordination to rhodium, have the propensity to exhibit promising biological activities [7–10] and they can also behave as a robust directing group (DG) to bring about CH bond activation as well as functionalization [11–20].
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Present address: Department of Chemistry, Massey University, Palmerston North, New Zealand.