scholarly journals Room Temperature Ni(II) Catalyzed Hydrophosphination and Cyclotrimerization of Alkynes

Inorganics ◽  
2018 ◽  
Vol 6 (4) ◽  
pp. 120 ◽  
Author(s):  
Ruth Webster
Keyword(s):  
Catalytic Activity ◽  
Room Temperature ◽  
Nickel Complexes ◽  
Metal Centers ◽  
Secondary Phosphines

The catalytic activity of nickel complexes in hydrophosphination involving secondary phosphines is not a commonly studied transformation. Beyond a small number of stand-out examples, many reports in the literature focus on the use of simple nickel salts. β-Diketiminates have been proven to be incredibly effective ligands for catalysis using a range of metal centers. This synthetic study investigates the catalytic ability of a Ni(II) β-diketiminate complex in the hydrophosphination of alkenes and alkynes, with a serendipitous discovery of its ability to effect alkyne cyclotrimerization and phosphine dehydrocoupling.

Nickel (II) and oxovanadium (IV) complexes supported on MCM-41 mesoporous and their application in catalytic selective sulfide and thiol oxidation

2020 ◽  
Vol 23 ◽  
Author(s):  
Mohsen Nikoorazm ◽  
Maryam Khanmoradi ◽  
Masoumeh Sayadian
Keyword(s):  
Catalytic Activity ◽  
Room Temperature ◽  
Sol Gel ◽  
Reaction Times ◽  
Significant Loss ◽  
Spectral Studies ◽  
High Catalytic Activity ◽  
Catalytic Systems ◽  
Solvent Free Conditions ◽  
Mcm 41

Introduction:: MCM-41 was synthesized using the sol-gel method. Then two new transition metal complexes of Nickel (II) and Vanadium (IV), were synthesized by immobilization of adenine (6-aminopurine) into MCM-41 mesoporous. The compounds have been characterized by XRD, TGA, SEM, AAS and FT-IR spectral studies. Using these catalysts provided an efficient and enantioselective procedure for oxidation of sulfides to sulfoxides and oxidative coupling of thiols to their corresponding disulfides using hydrogen peroxide at room temperature. Materials and Methods:: To a solution of sulfide or thiol (1 mmol) and H2O2 (5 mmol), a determined amount of the catalyst was added. The reaction mixture was stirred at room temperature for the specific time under solvent free conditions. The progress of the reaction was monitored by TLC using n-hexane: acetone (8:2). Afterwards, the catalyst was removed from the reaction mixture by centrifugation and, then, washed with dichloromethane in order to give the pure products. Results:: All the products were obtained in excellent yields and short reaction times indicating the high activity of the synthesized catalysts. Besides, the catalysts can be recovered and reused for several runs without significant loss in their catalytic activity. Conclusion:: These catalytic systems furnish the products very quickly with excellent yields and VO-6AP-MCM-41 shows high catalytic activity compared to Ni-6AP-MCM-41.

Synthesis, structural characterization and catalytic activity of chlororuthenium(II) complexes with substituted Schiff base/phosphine ancillary ligands

2020 ◽  
Vol 75 (9-10) ◽  
pp. 851-857
Author(s):  
Chong Chen ◽  
Fule Wu ◽  
Jiao Ji ◽  
Ai-Quan Jia ◽  
Qian-Feng Zhang
Keyword(s):  
Schiff Base ◽  
Catalytic Activity ◽  
Structural Characterization ◽  
Room Temperature ◽  
Molecular Structures ◽  
Cationic Complex ◽  
Neutral Complex ◽  
Ancillary Ligands ◽  
X Ray ◽  
X Ray Crystallography

AbstractTreatment of [(η6-p-cymene)RuCl2]2 with one equivalent of chlorodiphenylphosphine in tetrahydrofuran at reflux afforded a neutral complex [(η6-p-cymene)RuCl2(κ1-P-PPh2OH)] (1). Similarly, the reaction of [Ru(bpy)2Cl2·2H2O] (bpy = 2,2′-bipyridine) and chlorodiphenylphosphine in methanol gave a cationic complex [Ru(bpy)2Cl(κ1-P-PPh2OCH3)](PF6) (2), while treatment of [RuCl2(PPh3)3] with [2-(C5H4N)CH=N(CH2)2N(CH3)2] (L1) in tetrahydrofuran at room temperature afforded a ruthenium(II) complex [Ru(PPh3)Cl2(κ3-N,N,N-L1)] (3). Interaction of the chloro-bridged complex [Ru(CO)2Cl2]n with one equivalent of [Ph2P(o-C6H4)CH=N(CH2)2N(CH3)2] (L2) led to the isolation of [Ru(CO)Cl2(κ3-P,N,N-L2)] (4). The molecular structures of the ruthenium(II) complexes 1–4 have been determined by single-crystal X-ray crystallography. The properties of the ruthenium(II) complex 4 as a hydrogenation catalyst for acetophenone were also tested.

Dioxygen splitting at room temperature over distant binuclear transition metal centers in zeolites for direct oxidation of methane to methanol

2021 ◽  
Author(s):  
Kinga Mlekodaj ◽  
Mariia Lemishka ◽  
Stepan Sklenak ◽  
Jiri Dedecek ◽  
Edyta Tabor
Keyword(s):  
Transition Metal ◽  
Room Temperature ◽  
Direct Oxidation ◽  
Metal Centers ◽  
Oxidation Of Methane ◽  
First Time

Here we demonstrate for the first time the splitting of dioxygen at RT over distant binuclear transition metal (M = Ni, Mn, and Co) centers stabilized in ferrierite zeolite. Cleaved...

Catalytic activity of CuGHK peptide-based porous material

2021 ◽  
Author(s):  
Francisco G. Cirujano ◽  
Nuria Martin ◽  
Neyvis Almora-Barrios ◽  
Carlos Martí-Gastaldo
Keyword(s):  
Catalytic Activity ◽  
Porous Material ◽  
Active Sites ◽  
Room Temperature ◽  
Side Chain ◽  
Periodic Distribution ◽  
Lysine Side Chain ◽  
One Step

Room temperature one-step synthesis of the peptide-based porous material with a periodic distribution of pockets decorated with lysine side chain active sites behaves as a heterogeneous organocatalyst. The pockets are...

A Ag–Pd alloy supported on an amine-functionalized UiO-66 as an efficient synergetic catalyst for the dehydrogenation of formic acid at room temperature

2016 ◽  
Vol 6 (3) ◽  
pp. 869-874 ◽  
Author(s):  
Shu-Tao Gao ◽  
Weihua Liu ◽  
Cheng Feng ◽  
Ning-Zhao Shang ◽  
Chun Wang
Keyword(s):  
Catalytic Activity ◽  
Formic Acid ◽  
Room Temperature ◽  
High Catalytic Activity ◽  
Amine Functionalized ◽  
Pd Alloy

Ag–Pd alloys deposited on an amine-functionalized UiO-66(NH2–UiO-66) have been successfully prepared via a pre-coordination method and used as a AgPd@NH2–UiO-66 catalyst with 100% H2 selectivity and a high catalytic activity.

The remarkable catalytic activity of ultra-small free-CeO2 nanoparticles in selective carbon–carbon bond formation reactions in water at room temperature

2015 ◽  
Vol 39 (7) ◽  
pp. 5350-5353 ◽  
Author(s):  
Subhash Banerjee
Keyword(s):  
Catalytic Activity ◽  
Room Temperature ◽  
Bond Formation ◽  
Ceo2 Nanoparticles ◽  
Cerium Oxide Nanoparticles ◽  
Oxide Nanoparticles ◽  
Reusable Catalyst ◽  
Carbon Carbon Bond ◽  
Active Methylene Compounds ◽  
Active Methylene

A simple and efficient protocol for selective bis-Michael addition and mono-allylation of active methylene compounds has been demonstrated using ultra-small size (∼5 nm) uncapped cerium oxide nanoparticles (free-CeO2 NPs) as a reusable catalyst in water at room temperature.

scholarly journals A green approach to the synthesis of a nano catalyst and the role of basicity, calcination, catalytic activity and aging in the green synthesis of 2-aryl bezimidazoles, benzothiazoles and benzoxazoles

RSC Advances ◽  
2017 ◽  
Vol 7 (67) ◽  
pp. 42000-42012 ◽  
Author(s):  
Pramod K. Sahu
Keyword(s):  
Catalytic Activity ◽  
Green Synthesis ◽  
Room Temperature ◽  
Molar Ratios ◽  
Green Approach ◽  
Grinding Method ◽  
Nano Catalyst ◽  
Layered Catalyst

A green synthesis of hydrotalcite (a double layered catalyst) by a grinding method using Al/Mg molar ratios of 1.0–3.0 at room temperature is described.

A Magnetically Ordered Non-Stoichiometric Zinc Ferrite for the Oxidative Dehydrogenation Reactions.

2001 ◽  
Vol 676 ◽  
Author(s):  
J. A. Toledo ◽  
N. Nava ◽  
X. C. Sun ◽  
X. Bokhimi
Keyword(s):  
Catalytic Activity ◽  
Oxidative Dehydrogenation ◽  
Spinel Structure ◽  
Zinc Ferrite ◽  
Room Temperature ◽  
Annealing Temperature ◽  
Octahedral Sites ◽  
Tetrahedral Sites ◽  
Dehydrogenation Reactions ◽  
Hydrothermal Reduction

ABSTRACTZnFe2O4 nanoparticles were prepared by hydrothermal reduction approach. A considerable amount of α-Fe2O3 was segregated in the as-synthesized sample, which diffused into the tetrahedral and octahedral sites of the ZnFe2O4 spinel structure with increasing the annealing temperature. The introduction of Fe3+ into the tetrahedral positions was observed by Mössbauer spectra. Magnetization measurements showed an unusual ferrimagnetic behavior of the ZnFe2O4 phase, even at room temperature, confirming the introduction of Fe3+ into the tetrahedral sites of the spinel structure. Catalytic activity measured in the oxidative dehydrogenation of 1-butene reaction increased with increasing annealing temperature, indicating that those interactions of Fe3+ in tetrahedral and octahedral positions also promotes the activity and selectivity to butadiene formation.

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