The results of investigations about the polymerization of p-aminophenol in neutral-weak alkaline medium (pH = 7-8) in our lab showed that the produced polymer which was insoluble in water and soluble in methanol has high tendency to form selectively a blue complex with Ni(II). Investigations into the chemical structure of polymer showed that polymer has a special structure, similar to polyamine in which the aromatic rings are connected through O-bridges. Based on these data, it was decided to polymerize p-aminophenol in situ on graphene oxide (GO) and use as a new sorbent for selective separation and preconcentration of trace amount of Ni(II) from water samples. By this, the rate of sorption of Ni(II) will also be increased considerably with respect to GO alone. Resulting composite (GO-Pp-AP) was characterized by FT-IR, XRD, FE-SEM, and EDS. The obtained data confirmed the uniform growth of the polymer on the GO and the absence of granular particles. The composite shows high tendency and high rate of sorption of Ni(II) and consequently was utilized for solid phase extraction (SPE) of Ni(II) ions before its determination by flame atomic absorption (FAAS). The effects of important parameters on the recovery of Ni(II) were investigated. The presence of foreign ions has no meaningful effect on the recovery percentage of Ni(II). Under the optimum conditions, limit of detection and relative standard deviation were found to be 0.70 μg L and 1.8% (for n = 6; at 20 μg L of Ni(II)), respectively. Testing the standard reference material and analyzing the spiked real samples exhibit that the procedure can be successfully employed for determination of Ni(II) in natural water and wastewater samples. Graphical abstract ᅟ.
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http://dx.doi.org/10.1007/s10661-019-7282-x | DOI Listing |
J Am Chem Soc
January 2025
Dipartimento di Scienze Fisiche e Chimiche, Universita degli Studi dellAquila, Coppito, 67100 L'Aquila, Italy.
We present a comprehensive theoretical study, using state-of-the-art density functional theory simulations, of the structural and electrochemical properties of amorphous pristine and iron-doped nickel-(oxy)hydroxide catalyst films for water oxidation in alkaline solutions, referred to as NiCat and Fe:NiCat. Our simulations accurately capture the structural changes in locally ordered units, as reported by X-ray absorption spectroscopy, when the catalyst films are activated by exposure to a positive potential. We emphasize the critical role of proton-coupled electron transfer in the reversible oxidation of Ni(II) to Ni(III/IV) during this activation.
View Article and Find Full Text PDFCarbohydr Res
January 2025
Bioorganic Laboratory, Department of Chemistry, University of Delhi, Delhi, 110007, India; Department of Chemistry, Ramjas College, University of Delhi, Delhi, 110007, India. Electronic address:
Nickel, an essential transition metal, plays a vital role in biological systems and industries. However, exposure to nickel can cause severe health issues, such as asthma, dermatitis, pneumonitis, neurological disorders, and cancers of the nasal cavity and lungs. Due to nickel's toxicity and extensive industrial use, efficient sensors for detecting Ni ions in environmental and biological contexts are essential.
View Article and Find Full Text PDFInorg Chem
January 2025
University of Göttingen, Institute of Inorganic Chemistry, Tammannstrasse 4, D-37077 Göttingen, Germany.
Alkyl nickel intermediates relevant to catalytic processes often feature agostic stabilization, but relatively little is known about the situation in oligonickel systems. The dinickel(I) complex K[LNi], which is based on a compartmental pyrazolato-bridged ligand L with two β-diketiminato chelate arms, or its masked version, the dihydride complex [KL(Ni-H)] that readily releases H, oxidatively add methyl tosylate to give diamagnetic [LNi(CH)] () with (Ni···Ni) ≈ 3.7 Å.
View Article and Find Full Text PDFDalton Trans
January 2025
Departamento de Química Inorgánica, Universidad de Sevilla, 41012 Sevilla, Spain.
Preformed Ni(0) complexes are rarely used as precatalysts in cross-coupling reactions, although they can incorporate catalytically active nickel directly into the reaction. In this work, we focus on the preparation and the catalytic application of low-coordinate Ni(0) complexes supported by bulky monophosphine ligands in C-S cross-coupling reactions. We have prepared two families of Ni(0) complexes, bis-phosphine aducts of the type [Ni(PRAr')] (Ar' = -terphenyl group) and monophosphine derivatives of the type [Ni(PRAr')(DVDS)] (DVDS = divinyltetramethyldisiloxane).
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Chemistry, University College of Science, University of Calcutta, 92 A.P.C. Road, Kolkata 700009, India.
The well-known inhibitory strength of 3d metal Schiff base complexes against urease enzymes has long been acknowledged, but their untapped potential to act as ureolytic mimics of active metallobiosites remained unexplored. To break the new ground, we present pyrrolidine-based mononuclear Ni(II)-azide complex {[NiL(HL)(N)]·1.5(HO)} using the N,N,O donor ligand, namely ()-4-bromo-2-(((2-(pyrrolidin-1-yl)ethyl)imino)methyl)phenol.
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