![Catalysts | Free Full-Text | Palladium-Based Catalysts as Electrodes for Direct Methanol Fuel Cells: A Last Ten Years Review Catalysts | Free Full-Text | Palladium-Based Catalysts as Electrodes for Direct Methanol Fuel Cells: A Last Ten Years Review](https://pub.mdpi-res.com/catalysts/catalysts-06-00130/article_deploy/html/images/catalysts-06-00130-ag.png?1581080491)
Catalysts | Free Full-Text | Palladium-Based Catalysts as Electrodes for Direct Methanol Fuel Cells: A Last Ten Years Review
![Self-assembled palladium nanoflowers supported on fullerene: Electrochemical catalytic performance for the reduction of 4-nitrophenol - ScienceDirect Self-assembled palladium nanoflowers supported on fullerene: Electrochemical catalytic performance for the reduction of 4-nitrophenol - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S138824811930147X-ga1.jpg)
Self-assembled palladium nanoflowers supported on fullerene: Electrochemical catalytic performance for the reduction of 4-nitrophenol - ScienceDirect
![On the Mechanism of Palladium-Catalyzed Aromatic C−H Oxidation | Journal of the American Chemical Society On the Mechanism of Palladium-Catalyzed Aromatic C−H Oxidation | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja1054274/asset/images/large/ja-2010-054274_0001.jpeg)
On the Mechanism of Palladium-Catalyzed Aromatic C−H Oxidation | Journal of the American Chemical Society
![A visible-light activated secondary phosphine oxide ligand enabling Pd-catalyzed radical cross-couplings | Nature Communications A visible-light activated secondary phosphine oxide ligand enabling Pd-catalyzed radical cross-couplings | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-022-31613-9/MediaObjects/41467_2022_31613_Fig1_HTML.png)
A visible-light activated secondary phosphine oxide ligand enabling Pd-catalyzed radical cross-couplings | Nature Communications
![Redox trends in cyclometalated palladium( ii ) complexes - Dalton Transactions (RSC Publishing) DOI:10.1039/C6DT03786K Redox trends in cyclometalated palladium( ii ) complexes - Dalton Transactions (RSC Publishing) DOI:10.1039/C6DT03786K](https://pubs.rsc.org/image/article/2017/DT/c6dt03786k/c6dt03786k-f1_hi-res.gif)
Redox trends in cyclometalated palladium( ii ) complexes - Dalton Transactions (RSC Publishing) DOI:10.1039/C6DT03786K
![Inorganics | Free Full-Text | Redox-Induced Aromatic C–H Bond Functionalization in Metal Complex Catalysis from the Electrochemical Point of View Inorganics | Free Full-Text | Redox-Induced Aromatic C–H Bond Functionalization in Metal Complex Catalysis from the Electrochemical Point of View](https://pub.mdpi-res.com/inorganics/inorganics-05-00070/article_deploy/html/images/inorganics-05-00070-ag-550.jpg?1569603928)
Inorganics | Free Full-Text | Redox-Induced Aromatic C–H Bond Functionalization in Metal Complex Catalysis from the Electrochemical Point of View
![Can Donor Ligands Make Pd(OAc)2 a Stronger Oxidant? Access to Elusive Palladium(II) Reduction Potentials and Effects of Ancillary Ligands via Palladium(II)/Hydroquinone Redox Equilibria | Journal of the American Chemical Society Can Donor Ligands Make Pd(OAc)2 a Stronger Oxidant? Access to Elusive Palladium(II) Reduction Potentials and Effects of Ancillary Ligands via Palladium(II)/Hydroquinone Redox Equilibria | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.0c09464/asset/images/medium/ja0c09464_0011.gif)
Can Donor Ligands Make Pd(OAc)2 a Stronger Oxidant? Access to Elusive Palladium(II) Reduction Potentials and Effects of Ancillary Ligands via Palladium(II)/Hydroquinone Redox Equilibria | Journal of the American Chemical Society
![Tuning the Copper(II)/Copper(I) Redox Potential for More Robust Copper‐Catalyzed C–N Bond Forming Reactions - Cope - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library Tuning the Copper(II)/Copper(I) Redox Potential for More Robust Copper‐Catalyzed C–N Bond Forming Reactions - Cope - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/cc5e41d0-064d-4c84-8bad-7ac53525c09f/ejic201901269-toc-0001-m.jpg)
Tuning the Copper(II)/Copper(I) Redox Potential for More Robust Copper‐Catalyzed C–N Bond Forming Reactions - Cope - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library
![Can Donor Ligands Make Pd(OAc)2 a Stronger Oxidant? Access to Elusive Palladium(II) Reduction Potentials and Effects of Ancillary Ligands via Palladium(II)/Hydroquinone Redox Equilibria | Journal of the American Chemical Society Can Donor Ligands Make Pd(OAc)2 a Stronger Oxidant? Access to Elusive Palladium(II) Reduction Potentials and Effects of Ancillary Ligands via Palladium(II)/Hydroquinone Redox Equilibria | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.0c09464/asset/images/large/ja0c09464_0010.jpeg)
Can Donor Ligands Make Pd(OAc)2 a Stronger Oxidant? Access to Elusive Palladium(II) Reduction Potentials and Effects of Ancillary Ligands via Palladium(II)/Hydroquinone Redox Equilibria | Journal of the American Chemical Society
Solvent-Induced Reduction of Palladium-Aryls, a Potential Interference in Pd Catalysis | Organometallics
![Redox trends in cyclometalated palladium( ii ) complexes - Dalton Transactions (RSC Publishing) DOI:10.1039/C6DT03786K Redox trends in cyclometalated palladium( ii ) complexes - Dalton Transactions (RSC Publishing) DOI:10.1039/C6DT03786K](https://pubs.rsc.org/image/article/2017/DT/c6dt03786k/c6dt03786k-f9_hi-res.gif)
Redox trends in cyclometalated palladium( ii ) complexes - Dalton Transactions (RSC Publishing) DOI:10.1039/C6DT03786K
![Palladium-catalyzed asymmetric allylic 4-pyridinylation via electroreductive substitution reaction | Nature Communications Palladium-catalyzed asymmetric allylic 4-pyridinylation via electroreductive substitution reaction | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-022-33452-0/MediaObjects/41467_2022_33452_Fig1_HTML.png)