Investigation of the electrocatalytic reaction for the oxidation of alcohols through the formation of a metal organic framework (Mn-MIL-100)/polymer matrix on the surface of an Au electrode

An electrode composite containing a metal organic framework (Mn-MIL-100) was prepared by linkers including gold nanoparticles/polypyrrole and cysteine. The electrocatalytic application of this nanocomposite was evaluated via the oxidation of benzylic and aliphatic alcohols under open air conditions. Various active and inactive alcohol derivatives were successfully converted to the corresponding ketones with excellent yields. This advanced electrocatalyst proved to have remarkable stability over several recovery cycles from the reaction medium without significant change in its activity and selectivity and its regeneration potential. The active surface area of this electrocatalyst is very large due to its structural features, arising from the introduction of a metal organic framework (Mn-MIL-100) on a gold electrode, which provides more accessible surface sites, therefore boosting the electrocatalytic activity. The structure of the synthesized electrocatalyst has been characterized by FESEM, EDX, and AFM techniques. © 2023 The Royal Society of Chemistr

Topological insights in polynuclear Ni/Na coordination clusters derived from a schiff base ligand

This article presents the syntheses, crystal structures, topological features and magnetic properties of two NiII/NaI coordination clusters (CCs) formulated [NiII3Na(L1)3(HL1 (MeOH)2] (1) and [NiII6Na(L1)5(CO3)(MeO (MeOH)3(H2O)3]·4(MeOH) 2(H2O) [2 4(MeOH) 2(H2O)] where H2L1 is the semi rigid Schiff base ligand (E)-2-(2-hydroxy-3 methoxybenzylideneamino)-phenol). Compound 1 possesses a rare NiII3NaI cubane (3M4-1) topology and compound 2 is the first example in polynuclear Ni/Na chemistry that exhibits a 2,3,4M7-1 topology

Synthesis of Two Potentially Heptadentate (N4O3) Schiff-base Ligands Derived from Condensation of Tris(3-aminopropyl)-amine and Salicylaldehyde or 4-Hydroxysalicylaldehyde. Nickel(II) and Copper(II) Complexes of the Former Ligand

Two potentially heptadentate (N4O3) tripodal Schiff-base ligands: tris(3-(salicylideneimino)propyl)amine (H3L1) and tris(3-(4’-hydroxysalicylideneimino)-propyl)amine (H3L2) have been prepared and characterized by various spectroscopic methods (IR, FAB-MS, NMR). They are derived from the condensation reactions of tris(3-aminopropyl)amine (tpt), with 3 equivalents of either salicylaldehyde or the ringsubstituted salicylaldehyde, 4-hydroxysalicylaldehyde. The nickel(II) and copper(II) complexes of H3L1 were obtained from the its reactions Ni(II) and Cu(II) salts in absolute methanol. These complexes were studied by IR and FAB-Mass spectrometry

Analyzing Capacity Withholding in Oligopoly Electricity Markets Considering Forward Contracts and Demand Elasticity

In this paper capacity withholding in an oligopolistic electricity market that all Generation Companies (GenCos) bid in a Cournot model is analyzed and the capacity withheld index, the capacity distortion index and the price distortion index are obtained and formulated. Then a new index, Distortion-Withheld Index (DWI), is proposed in order to measure the potential ability of market for capacity withholding. In these indices the impact of demand elasticity on capacity withholding is considered and it is shown that demand elasticity plays an important role for capacity withholding and market power mitigation. Due to the significant role of forward contracts for market power mitigation and risk hedging in power markets, the impacts of these contracts on capacity withholding are considered. The effects of GenCos’ strategic forward contracts on capacity withholding are also discussed. Moreover, the relationship between capacity withholding of GenCos and market price distortion is acquired. A two-settlement market including a forward market and a spot market is used to describe GenCos’ strategic forward contracting and spot market competition

Synthesis and Crystal Structure Determination of a Nickel(II) Complex of an Acyclic Pentadentate (N5) Mono Schiff Base Ligand.

Abstract: The asymmetrical tripodal tetraamine ligand N[(CH2)3NH2]2[(CH2)2NH2] (ppe) was condensed with 2-acetylpyridine in the presence of nickel(II) ion. In ethanolwater solution the reaction stops after the first stage of condensation, and a new nickel(II) complex of an acyclic pentadentate (N5) mono Schiff base ligand was obtained. X-ray structure analysis of the resulting complex, [Ni(ppe-py)(H2O)](ClO4)2, indicates that condensation with 2-acetylpyridine is at the propylene chain of ppe. The geometry around the nickel ion is distorted octahedral in which the sixth co-ordination group is a solvent molecule