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One to Find Them All: A General Route to Ni(I)–Phenolate Species | Journal  of the American Chemical Society
One to Find Them All: A General Route to Ni(I)–Phenolate Species | Journal of the American Chemical Society

Ni(acac)2 | C10H14NiO4 | ChemSpider
Ni(acac)2 | C10H14NiO4 | ChemSpider

Carboxylation of the Ni–Me Bond in an Electron-Rich Unsymmetrical PCN  Pincer Nickel Complex | Organometallics
Carboxylation of the Ni–Me Bond in an Electron-Rich Unsymmetrical PCN Pincer Nickel Complex | Organometallics

BPhen)Ni(OAc)2.xH2O 2304339-11-3
BPhen)Ni(OAc)2.xH2O 2304339-11-3

Synthesis, crystal structure, spectroscopic investigations, and  computational studies of Ni(II) and Pd(II) complexes with asymmetric  tetradentate NOON Schiff base ligand | SpringerLink
Synthesis, crystal structure, spectroscopic investigations, and computational studies of Ni(II) and Pd(II) complexes with asymmetric tetradentate NOON Schiff base ligand | SpringerLink

Catalysts | Free Full-Text | Synthesis and Characterization of Nickel(II)  Homogeneous and Supported Complexes for the Hydrogenation of Furfural to  Furfuryl Alcohol
Catalysts | Free Full-Text | Synthesis and Characterization of Nickel(II) Homogeneous and Supported Complexes for the Hydrogenation of Furfural to Furfuryl Alcohol

Synthesis, molecular structure and electrochemical properties of nickel( ii  ) benzhydrazone complexes: influence of ligand substitution on DNA/protein  ... - RSC Advances (RSC Publishing) DOI:10.1039/C5RA19530F
Synthesis, molecular structure and electrochemical properties of nickel( ii ) benzhydrazone complexes: influence of ligand substitution on DNA/protein ... - RSC Advances (RSC Publishing) DOI:10.1039/C5RA19530F

Polymers | Free Full-Text | Mononuclear Nickel(II) Complexes with Schiff  Base Ligands: Synthesis, Characterization, and Catalytic Activity in  Norbornene Polymerization
Polymers | Free Full-Text | Mononuclear Nickel(II) Complexes with Schiff Base Ligands: Synthesis, Characterization, and Catalytic Activity in Norbornene Polymerization

Synthesis of bridged tricyclo[5.2.1.01,5]decanes via nickel-catalyzed  asymmetric domino cyclization of enynones | Nature Communications
Synthesis of bridged tricyclo[5.2.1.01,5]decanes via nickel-catalyzed asymmetric domino cyclization of enynones | Nature Communications

Nickel (II) Acetylacetonate | FAR Chemical
Nickel (II) Acetylacetonate | FAR Chemical

Ni‐Catalyzed Regioselective C‐5 Halogenation of 8‐Aminoquinoline and  Co‐Catalyzed Chelation Assisted C−H Iodination of Aromatic Sulfonamides  with Molecular Iodine - Fernandes - 2022 - Chemistry – An Asian  Journal - Wiley Online Library
Ni‐Catalyzed Regioselective C‐5 Halogenation of 8‐Aminoquinoline and Co‐Catalyzed Chelation Assisted C−H Iodination of Aromatic Sulfonamides with Molecular Iodine - Fernandes - 2022 - Chemistry – An Asian Journal - Wiley Online Library

Solved a.) Nickel acetate tetrahydrate has an octahedral | Chegg.com
Solved a.) Nickel acetate tetrahydrate has an octahedral | Chegg.com

Naked d-orbital in a centrochiral Ni(II) complex as a catalyst for  asymmetric [3+2] cycloaddition | Nature Communications
Naked d-orbital in a centrochiral Ni(II) complex as a catalyst for asymmetric [3+2] cycloaddition | Nature Communications

Electrocatalytic water oxidation by a Ni(ii) salophen-type complex - RSC  Advances (RSC Publishing)
Electrocatalytic water oxidation by a Ni(ii) salophen-type complex - RSC Advances (RSC Publishing)

Reactions of Schiff Base‐Substituted Diselenides and ‐tellurides with Ni(II),  Pd(II) and Pt(II) Phosphine Complexes - Roca Jungfer - 2020 - European  Journal of Inorganic Chemistry - Wiley Online Library
Reactions of Schiff Base‐Substituted Diselenides and ‐tellurides with Ni(II), Pd(II) and Pt(II) Phosphine Complexes - Roca Jungfer - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library

Scheme 1 Synthesis of nickel(II) thiocarboxamide complexes. | Download  Scientific Diagram
Scheme 1 Synthesis of nickel(II) thiocarboxamide complexes. | Download Scientific Diagram

CAS: 6018-89-9 - nickel acetate | CymitQuimica
CAS: 6018-89-9 - nickel acetate | CymitQuimica

Nickel(II) bis(acetylacetonate) - Wikipedia
Nickel(II) bis(acetylacetonate) - Wikipedia

Nickel(II) acetate 98 6018-89-9
Nickel(II) acetate 98 6018-89-9

Nickel-Catalyzed Biaryl Coupling of Heteroarenes and Aryl Halides/Triflates  | Itami Organic Chemistry Laboratory, Nagoya University
Nickel-Catalyzed Biaryl Coupling of Heteroarenes and Aryl Halides/Triflates | Itami Organic Chemistry Laboratory, Nagoya University

IJMS | Free Full-Text | Mild and Efficient Heterogeneous Hydrogenation of  Nitroarenes Facilitated by a Pyrolytically Activated Dinuclear Ni(II)-Ce(III)  Diimine Complex
IJMS | Free Full-Text | Mild and Efficient Heterogeneous Hydrogenation of Nitroarenes Facilitated by a Pyrolytically Activated Dinuclear Ni(II)-Ce(III) Diimine Complex

Stereospecific/stereoselective nickel catalyzed reductive cross-coupling:  An efficient tool for the synthesis of biological active targeted molecules  - ScienceDirect
Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules - ScienceDirect

Ni(II)-Catalyzed Intramolecular C–H/C–H Oxidative Coupling: An Efficient  Route to Functionalized Cycloindolones and Indenoindolones | ACS Catalysis
Ni(II)-Catalyzed Intramolecular C–H/C–H Oxidative Coupling: An Efficient Route to Functionalized Cycloindolones and Indenoindolones | ACS Catalysis

4,4 -Bis(1,1-dimethylethyl)-2,2 -bipyridine nickel (II) dichloride  1034901-50-2
4,4 -Bis(1,1-dimethylethyl)-2,2 -bipyridine nickel (II) dichloride 1034901-50-2

Nickel hydroxides and related materials: a review of their structures,  synthesis and properties | Proceedings of the Royal Society A:  Mathematical, Physical and Engineering Sciences
Nickel hydroxides and related materials: a review of their structures, synthesis and properties | Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences

Ni(OAc)2: a highly efficient catalyst for the synthesis of enaminone and  enamino ester derivatives under solvent‐free conditions - Liu - 2010 -  Applied Organometallic Chemistry - Wiley Online Library
Ni(OAc)2: a highly efficient catalyst for the synthesis of enaminone and enamino ester derivatives under solvent‐free conditions - Liu - 2010 - Applied Organometallic Chemistry - Wiley Online Library