![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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs11224-019-01350-9/MediaObjects/11224_2019_1350_Sch1_HTML.png)
Synthesis, crystal structure, spectroscopic investigations, and computational studies of Ni(II) and Pd(II) complexes with asymmetric tetradentate NOON Schiff base ligand | SpringerLink
![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](https://onlinelibrary.wiley.com/cms/asset/8edc1e26-d2b5-40a5-adc7-5863764cb759/asia202200874-toc-0001-m.jpg)
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
![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](https://ars.els-cdn.com/content/image/1-s2.0-S1319610322001715-gr38.jpg)
Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules - ScienceDirect
![SYNTHESIS, SPECTROSCOPIC INVESTIGATION AND CATALYTIC STUDIES OF NICKEL(II) AROMATIC AZOMETHINE COMPLEXES | Semantic Scholar SYNTHESIS, SPECTROSCOPIC INVESTIGATION AND CATALYTIC STUDIES OF NICKEL(II) AROMATIC AZOMETHINE COMPLEXES | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/381decb84a74f5a2b51f96fecbbb725c07e2a801/3-Figure2-1.png)
SYNTHESIS, SPECTROSCOPIC INVESTIGATION AND CATALYTIC STUDIES OF NICKEL(II) AROMATIC AZOMETHINE COMPLEXES | Semantic Scholar
![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](https://www.mdpi.com/polymers/polymers-09-00105/article_deploy/html/images/polymers-09-00105-sch003-550.jpg)
Polymers | Free Full-Text | Mononuclear Nickel(II) Complexes with Schiff Base Ligands: Synthesis, Characterization, and Catalytic Activity in Norbornene Polymerization
![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](https://www.mdpi.com/ijms/ijms-23-08742/article_deploy/html/images/ijms-23-08742-sch002.png)
IJMS | Free Full-Text | Mild and Efficient Heterogeneous Hydrogenation of Nitroarenes Facilitated by a Pyrolytically Activated Dinuclear Ni(II)-Ce(III) Diimine Complex
![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](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fncomms14875/MediaObjects/41467_2017_Article_BFncomms14875_Fig5_HTML.jpg)
Naked d-orbital in a centrochiral Ni(II) complex as a catalyst for asymmetric [3+2] cycloaddition | Nature Communications
One to Find Them All: A General Route to Ni(I)–Phenolate Species | Journal of the American Chemical Society
![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](https://royalsocietypublishing.org/cms/asset/0db42d86-7e10-442b-a2f6-a096fdf8bac6/rspa20140792f10.jpg)
Nickel hydroxides and related materials: a review of their structures, synthesis and properties | Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences
![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](https://pubs.acs.org/cms/10.1021/acs.organomet.9b00817/asset/images/medium/om9b00817_0005.gif)
Carboxylation of the Ni–Me Bond in an Electron-Rich Unsymmetrical PCN Pincer Nickel Complex | Organometallics
![General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis](https://www.organic-chemistry.org/abstracts/lit8/598o.gif)
General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis
![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](https://pub.mdpi-res.com/catalysts/catalysts-11-00684/article_deploy/html/images/catalysts-11-00684-ag-550.jpg?1622193468)
Catalysts | Free Full-Text | Synthesis and Characterization of Nickel(II) Homogeneous and Supported Complexes for the Hydrogenation of Furfural to Furfuryl Alcohol
![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](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/156ed1f1-3886-41bd-b27c-f0569350fc0d/ejic202000750-toc-0001-m.png)
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
![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](https://pubs.rsc.org/image/article/2015/RA/c5ra19530f/c5ra19530f-s1_hi-res.gif)