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Abstract: Pyridinecarbonitriles (pyCN), also referred to as cyanopyridines, are promising ligands for the formation of pyridine-based coordination compounds due to their two different N-donor atoms, which enable versatile coordination modes. Copper(II) complexes containing pyCN derivatives are of particular interest for their potential applications in medicinal chemistry and materials science. In this study, the synthesis, structural characterization, and thermal and magnetic properties of three new copper(II) complexes with 3-pyCN, 4-pyCN, and ethyl picolinimidate, obtained in situ by means of alcoholysis of 2-pyCN, are reported: [Cu2(μ-Ac)4(3-pyCN)2] (1), [Cu(H2O)2(Etpic)2]NO3 (2), and [Cu(NO3)2(CH3CN)(4-pyCN)2]·CH3CN (3). Single-crystal X-ray diffraction confirmed that complex 1 features a dinuclear paddle-wheel structure with bridging acetato ligands and monodentate 3-pyCN molecules, coordinated through the ring nitrogen, while complexes 2 and 3 are mononuclear. Thermal analysis showed an intense and highly exothermic decomposition of complex 3, containing nitrate ligands. Magnetic measurements revealed strong antiferromagnetic coupling in the dinuclear complex 1, whereas complexes 2 and 3 displayed paramagnetic behavior with effective magnetic moments ranging from 1.8 μB to 2.0 μB, consistent with isolated Cu(II) centers.
Keywords: copper(II) coordination compounds, cyanopyridines, crystal structure, magnetic properties, thermogravimetric analysis
Published in DKUM: 29.08.2025; Views: 0; Downloads: 4
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Abstract: As electrochemical CO2 reduction (ECR) nears industrialisation levels, addressing the uncontrolled stability, restructuring, and deactivation of copper (Cu) catalysts during operation becomes as crucial as achieving high activity and selectivity for a single product. This study used a high-surface area Cu catalyst that exhibited changes in ECR product selectivity over prolonged operation. The detection of dissolved Cu species during electrolysis confirmed an intermediates-mediated Cu dissolution mechanism at ECR potentials (−0.8 to −1.1 V vs. reversible hydrogen electrode). The findings suggest that the electrodeposition of dissolved Cu species is biased towards Cu catalyst sites with lower reaction intermediates coverage, e.g. adsorbed CO (*CO). A dynamic equilibrium between dissolution and subsequent selective redeposition gradually led to morphological restructuring, resulting in a shift in selectivity away from ECR and towards hydrogen production. With the obtained extensive experimental results, theoretical modelling, and literature data, four interconnected parameters governing restructuring and selectivity shifts were recognised: (i) size and (ii) crystallographic orientation of facets rsc.li/materials-a Introduction of the nanoparticles, (iii) *CO coverage and (iv) CObridge vs. COatop ratio.
Keywords: elektrokemija, katalizatorji, baker, proizvodnja vodika, electrochemistry, catalysts, copper, hydrogen production
Published in DKUM: 20.03.2025; Views: 0; Downloads: 4
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Abstract: Herein, a comparative analysis of two case example catalysts for electrocatalytic hydrogenation (ECH) of furfural under acidic conditions, namely a copper polycrystalline disc and copper nanoparticles dispersed on carbon support, is performed. To gain a detailed insight on ECH trends, a task-specific methodology is employed based on electrochemistry–mass spectrometry coupling, which enabled time- and potential-resolved detection of volatile ECH products, i.e., 2-methylfurane (2-MF) and H2. In this way, the ability to elucidate potential-dependent product distribution for the two catalysts, namely faradaic efficiency, is achieved. Accordingly, the nanoparticulate analog is significantly more active toward competitive hydrogen evolution reaction and 2-MF production, whereas the polycrystalline sample is more selective toward furfuryl alcohol. The observed differences in ECH are ascribed to alterations in surface domains, which is supported by surface-sensitive lead underpotential deposition characterization.
Keywords: baker, nanodelci, elektrokataliza, copper, nanoparticles, electrocatalytic hydrogeneration
Published in DKUM: 19.04.2024; Views: 161; Downloads: 11
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Abstract: The long-term use of copper (Cu) fungicides in viticulture in Europe has led to Cu accumulation in vineyard top soils. However, less is known about the accumulation of Cu in grapevine grafts after the callusing process/before planting in the nursery. This paper presents the capacity of 5BB and SO4 rootstocks to accumulate Cu, as well as the patterns of translocation in the grafts. After heat forcing (callusing), the grapevine grafts of Sauvignon Blanc on 5BB and SO4 rootstocks were grown in pots for six months in a glasshouse and exposed to various Cu formulations (Cu-oxychloride, Cu-gluconate) and concentrations in peat (50, 150, 500, and 1000 mg Cu of dry weight (DW)). In addition to monitoring the shoot growth dynamics and analyzing the copper content in graft organs, bioaccumulation (BAFs) and translocation factors (TFs) of Cu were calculated. The mean Cu concentrations were ranked as follows: roots (15–164) > rootstock trunks (8–38) > canes (5–21) mg kg−1 DW. The Cu concentrations depended on the Cu formulation and concentration in the substrate. Higher Cu content was found in the roots of both rootstocks (5BB and SO4, 23–155 and 15–164 mg kg−1 DW, respectively) and the lowest in the canes (less than 10 mg kg−1 DW) of grafts grown in Cu-oxychloride-treated peat. Based on the BAFs and TFs, both rootstocks could be considered as Cu exclusive. A higher translocation rate was determined in systemic Cu-gluconate and SO4 rootstock. With shoot length measurements, the significant inhibitory effects of Cu on grapevine grafts growth could not be confirmed, despite the inhibitory effects that were clearly expressed in the first two months of growth. Soils containing more than 500 mg Cu/kg−1 are less suitable for growing vine grafts.
Keywords: grapevine grafts, copper accumulation, Cu-oxychloride, Cu-gluconate, 5BB and SO4 rootstocks
Published in DKUM: 08.12.2023; Views: 457; Downloads: 32
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Abstract: In the manufacturing industry of electrical contacts, the prohibition of the use of toxic metals (Cd, Be), and desire to avoid the alloying with precious metals (Ag) has created a need for new alloys with good electrical conductivity and high mechanical properties at elevated temperatures. As a potentially useful material for this purpose, we have analyzed the continuously cast Cu-Fe-Ni-P alloy in various heat treatment conditions. Sequence of phase transformations during heat treatment was followed by 4 point D.C. electrical resistivity measuring method, and analyzed by scanning (SEM) and transmission (TEM) electron microscopy. Measurements of Vickers hardness and electrical conductivity after various heat treatment procedures indicate on high potential of Cu-Fe-Ni-P alloys as a material for electrical contacts.
Keywords: copper alloys, precipitation hardening, electrical contacts, electrical conductivity
Published in DKUM: 03.07.2017; Views: 2320; Downloads: 101
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