16 research outputs found

    Analyzing Related Strategic Behavior Through Strictly Alternating Interactions with Two-Memory Length

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    Reciprocal altruism can often be modeled through the iterated Prisoner’s Dilemma game in which players take turns in the roles of donor and recipient. Several late studies were based on memory alteration in the repeated Prisoner’s Dilemma game. This prompted us to study this alteration in a strictly alternating iterated Prisoner’s Dilemma game. In our work, we represented the repeated games played by finite states of automata. Also, we supposed that there is relatedness between the players in this game. A relatedness average degree r considered between players, where 0 ≤ r ≤ 1. The effect of noise on the relatedness degree among players can be examined with regard to the behavior of the strategies in their competitions

    Thiosemicarbazone copper complexes as competent catalysts for olefin cyclopropanations

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    New copper complexes of several thiosemicarbazones have been prepared and characterized. All complexes have been prepared by employing Cu (II) acetate hydrate, but analytical and spectroscopical data for the isolated complexes revealed that in most cases a reduction to copper (I) occurred. Cyclopropanation reactions of several olefins by ethyldiazoacetate (EDA) in the presence of catalytic amounts of the complexes were examined. The reported results showed that all complexes are competent catalysts for the cyclopropanation reaction of unactivated olefins. Cyclopropanes were obtained in high yields (up to 97%, TON up to 18,400) with moderate to excellent diastereoselectivities (up to >99%)

    Lightweight alkali-activated materials and ordinary Portland cement composites using recycled polyvinyl chloride and waste glass aggregates to fully replace natural sand

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    Data availability: Data will be made available on request.Copyright © 2023 The Authors. Polyvinyl chloride plastic (PVC) and glass waste have proven to be significant environmental concerns considering their restricted reuse and complicated recycling procedures. Glass and PVC waste materials form a substantial portion of total solid wastes that negatively influence the environment. This study aims to fully replace natural sand with recycled PVC and waste glass aggregates in alkali-activated materials (AAMs). A comprehensive testing programme was employed to investigate the effect of 100 % aggregate replacement on the composites’ mechanical performance, water absorption, impact resistance, thermal conductivity, resistance to harsh environments, and microstructural changes. Results revealed that AAMs containing recycled PVC and glass aggregates outperformed their ordinary Portland cement (OPC)-based composite counterparts in terms of mechanical properties, energy absorption, thermal conductivity, and carbon footprint estimation. Although mixtures containing recycled aggregates cannot be deemed for load-bearing applications, these composites exhibited a promising capacity to be used in insulating applications. AAMs containing 100 vol-% PVC aggregates with flexural and compressive strengths of 9 and 11 MPa, respectively, registered the highest energy absorption of about 6 J, three times higher than the AAM control sample, and the lowest thermal conductivity of about 0.5 W/mK, with about 80 % reduction of thermal conductivity compared to the AAM control sample. With the full replacement of PVC and glass aggregates, the most significant decrease in the carbon footprint is achieved for AAM (−352.25 kg CO2-eq) and OPC (−353.94 kg CO2-eq), respectively.DigiMat project, which has received funding from the European Union's Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement ID: 101029471

    On soft b* - continuous functions in soft topological spaces

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    In this paper, we study some of new types of continuous functions called soft b*−continuous functions and define soft b*−irresolute and discussed their relations with existing soft continuous and other weaker forms of soft continuous functions and some related properties are discussed. Also, we study soft b*−irresolute and soft b*−openmap and b*−closedmap and the relationships between them are discuss. We hope that the findings in this work will help researcher enhance and promote the further study on soft topological spaces to carry out a general framework for their applications in separation axioms, connectedness

    Synthesis and characterization of new Schiff base metal complexes and their use as catalysts for olefin cyclopropanation

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    New transition metal complexes of CoII, CuII, NiII and VIVO with the Schiff base, HL, 3-acetylcoumarin-N(4)-phenylthiosemicarbazone have been prepared. Characterization of the HL ligand and its complexes is also reported. Mass spectra and NMR assignments for the ligand, using COSY, NOESY homonuclear and HMQC and HMBC heteronuclear correlation techniques were carried out. Electronic and magnetic moments of the complexes indicate that the geometries of the metal centres are either distorted octahedral, square pyramidal, square planar or tetrahedral. The structures are consistent with the IR, UV-VIS, ESR, as well as conductivity and magnetic moments measurements. Cyclopropanation reactions of unactivated olefins by ethyldiazoacetate (EDA) in the presence of LCuIICl as catalyst proceed with excellent TON (up to 9625)

    Synthesis and characterization of some transition metal complexes with a novel Schiff base ligand and their use as catalysts for olefin cyclopropanation

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    A novel ligand HL (1), N,2-bis(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinecarbothioamide was synthesized through the condensation of 3-acetyl-2H-chromen-2-one and hydrazinecarbothioamide. This ligand was used to prep. new transition metal complexes of Cu(II), Ni(II) and Co(II). Characterization of the HL (1) ligand and its complexes is also reported. Mass spectra and NMR assignments for the ligand, using COSY, NOESY homonuclear and HMQC and HMBC heteronuclear correlation techniques were carried out. Electronic and magnetic moments of the complexes indicate that the geometries of the metal centers are either distorted octahedral, or square planar. The structures are consistent with the IR, UV-vis, ESR, as well as cond. measurements. The catalytic activity of the copper complex, [HLCu2Cl3]Cl.H2O (2), in cyclopropanation reactions of unactivated olefins with ethyldiazoacetate (EDA) was studied. Cyclopropanes were obtained in high yield (up to 97%, TON up to 16,900) with moderate to good diastereoselectivities (50-91%)

    Efficient cyclopropanation and intermolecular C-H bond activation via carbene insertion catalysed by thiosemicarbazone Copper complexes

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    Cyclopropane derivatives are an important family of chemical compounds that plays a prominent role in organic chemistry.1 As a result, great efforts have been made to develop efficient stereoselective methods for the synthesis of cyclopropanes.2 A particularly versatile method is the metal-catalysed cyclopropanation of olefins with diazo compounds, for which several efficient homogeneous catalysts have been developed.3 Among transition metal catalysts for this reaction, copper complexes have attracted increasing interest in the last years, especially due to their high efficiency and to their lower cost when compared to other metal derivatives. A variety of copper(II) and copper(I) sources are known to catalyse the cyclopropanation reaction although copper(I) rather than copper(II) was established as the active catalyst, where diazo compounds were found to reduce Cu(II) salts to Cu(I).4 Nevertheless Cu(I) complexes are challenging to synthesize and isolate due to the intrinsic instability of cuprous compounds: under many conditions disproportionation of Cu(I) to Cu(0) and Cu(II) is thermodynamically favoured. We have recently reported that Schiff bases derived from the condensation of hydrazinecarbothioamide or phenyl thiosemicarbazone with 3-acetyl-2H-chromen-2-one are suitable ligands for the synthesis of copper(II) complexes very active as cyclopropanation catalysts.5 We herein report that Schiff bases derived from the condensation reaction of hydrazinecarbothioamide with substituted salicylaldehydes are suitable ligands for copper and that the derived complexes are competent catalysts for the cyclopropanation of olefins and for the intermolecular C-H bond activation by using ethyldiazoacetate (EDA) as carbene source. Rarely metal complexes can give high selectivities in cyclopropanation reactions together with high turnover number (TON). In this work, different ligands have been synthesized and characterized, by changing the steric and electronic properties of the starting aldehyde employed in the condensation reaction. Their copper complexes have been prepared by employing Cu(II) acetate hydrate, but analytical and spectroscopical data for the isolated complexes revealed that in most cases a reduction to copper (I) occurred. Cyclopropanation reactions of several olefins by ethyldiazoacetate (EDA) in the presence of catalytic amounts of the complexes were examined. The reported results showed that all complexes are competent catalysts for the cyclopropanation reaction of unactivated olefins. Cyclopropanes were obtained in high yields (up to 97 %, TON up to 18,400) with moderate to excellent diastereoselectivities (up to >99%). Moreover, we have tested the catalytic capabilities of this copper-based system toward the activation of cycloalkanes and cyclic ethers and have found moderate-to-good degrees of conversion under very mild conditions
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