![The mechanism of palladium(II)-mediated C–H cleavage with mono-N-protected amino acid (MPAA) ligands: origins of rate acceleration in: Pure and Applied Chemistry Volume 88 Issue 1-2 (2016) The mechanism of palladium(II)-mediated C–H cleavage with mono-N-protected amino acid (MPAA) ligands: origins of rate acceleration in: Pure and Applied Chemistry Volume 88 Issue 1-2 (2016)](https://www.degruyter.com/view/journals/pac/88/1-2/graphic/j_pac-2015-0902_fig_009.jpg)
The mechanism of palladium(II)-mediated C–H cleavage with mono-N-protected amino acid (MPAA) ligands: origins of rate acceleration in: Pure and Applied Chemistry Volume 88 Issue 1-2 (2016)
![Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs42004-020-0287-0/MediaObjects/42004_2020_287_Fig2_HTML.png)
Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry
![Ligand screening for palladium nanocatalysts towards selective hydrogenation of alkynes - ScienceDirect Ligand screening for palladium nanocatalysts towards selective hydrogenation of alkynes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2468823120301772-ga1.jpg)
Ligand screening for palladium nanocatalysts towards selective hydrogenation of alkynes - ScienceDirect
![The role of amide ligands in the stabilization of Pd(II) tricoordinated complexes: is the Pd–NR 2 bond order single or higher? | SpringerLink The role of amide ligands in the stabilization of Pd(II) tricoordinated complexes: is the Pd–NR 2 bond order single or higher? | SpringerLink](https://media.springernature.com/full/springer-static/image/art%3A10.1007%2Fs00214-009-0539-7/MediaObjects/214_2009_539_Figa_HTML.gif)
The role of amide ligands in the stabilization of Pd(II) tricoordinated complexes: is the Pd–NR 2 bond order single or higher? | SpringerLink
![Palladium(II) complexes containing different types of nitrogen ligands... | Download Scientific Diagram Palladium(II) complexes containing different types of nitrogen ligands... | Download Scientific Diagram](https://www.researchgate.net/profile/Adnan_Abu-Surrah/publication/233729305/figure/fig3/AS:393364030672906@1470796701442/PalladiumII-complexes-containing-different-types-of-nitrogen-ligands-12-18_Q640.jpg)
Palladium(II) complexes containing different types of nitrogen ligands... | Download Scientific Diagram
![Neutral, cationic and anionic organonickel and -palladium complexes supported by iminophosphine/phosphinoenaminato ligands - Dalton Transactions (RSC Publishing) Neutral, cationic and anionic organonickel and -palladium complexes supported by iminophosphine/phosphinoenaminato ligands - Dalton Transactions (RSC Publishing)](https://pubs.rsc.org/image/article/2020/dt/c9dt04062e/c9dt04062e-s3_hi-res.gif)
Neutral, cationic and anionic organonickel and -palladium complexes supported by iminophosphine/phosphinoenaminato ligands - Dalton Transactions (RSC Publishing)
![Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate. - Abstract - Europe PMC Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3779523/bin/nihms476312f24.jpg)
Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate. - Abstract - Europe PMC
![Switching the Reactivity of Palladium Diimines with “Ancillary” Ligand to Select between Olefin Polymerization, Branching Regulation, or Olefin Isomerization - Jones - - Angewandte Chemie - Wiley Online Library Switching the Reactivity of Palladium Diimines with “Ancillary” Ligand to Select between Olefin Polymerization, Branching Regulation, or Olefin Isomerization - Jones - - Angewandte Chemie - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/1a7b4096-6725-41f0-b81e-a2fc13b26c2f/ange202012400-toc-0001-m.png)
Switching the Reactivity of Palladium Diimines with “Ancillary” Ligand to Select between Olefin Polymerization, Branching Regulation, or Olefin Isomerization - Jones - - Angewandte Chemie - Wiley Online Library
![Sulfur-Functionalized N-Heterocyclic Carbene Complexes of Pd(II): Syntheses, Structures and Catalytic Activities – topic of research paper in Chemical sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub. Sulfur-Functionalized N-Heterocyclic Carbene Complexes of Pd(II): Syntheses, Structures and Catalytic Activities – topic of research paper in Chemical sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub.](https://cyberleninka.org/viewer_images/526297/f/1.png)
Sulfur-Functionalized N-Heterocyclic Carbene Complexes of Pd(II): Syntheses, Structures and Catalytic Activities – topic of research paper in Chemical sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub.
![Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate. - Abstract - Europe PMC Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3779523/bin/nihms476312f13.jpg)
Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate. - Abstract - Europe PMC
![Molecular ligand modulation of palladium nanocatalysts for highly efficient and robust heterogeneous oxidation of cyclohexenone to phenol | Science Advances Molecular ligand modulation of palladium nanocatalysts for highly efficient and robust heterogeneous oxidation of cyclohexenone to phenol | Science Advances](https://advances.sciencemag.org/content/3/1/e1600615/F1.large.jpg)
Molecular ligand modulation of palladium nanocatalysts for highly efficient and robust heterogeneous oxidation of cyclohexenone to phenol | Science Advances
![Formation of palladium complexes of ligands 2a, 5 and 7. (A) Formation... | Download Scientific Diagram Formation of palladium complexes of ligands 2a, 5 and 7. (A) Formation... | Download Scientific Diagram](https://www.researchgate.net/publication/301739475/figure/fig3/AS:667602456166401@1536180237026/Formation-of-palladium-complexes-of-ligands-2a-5-and-7-A-Formation-of-2a-PdCl-2.png)
Formation of palladium complexes of ligands 2a, 5 and 7. (A) Formation... | Download Scientific Diagram
Cationic Two-Coordinate Complexes of Pd(I) and Pt(I) Have Longer Metal- Ligand Bonds Than Their Neutral Counterparts
A study of the platinum (II), palladium (II), and rhodium (III) chelates of aspartic and glutamic acid
![Platinum(II), palladium(II) and gold(I) benzimidazolin-2-ylidene as potential probes for determination of N-heterocyclic carbene donor strengths and steric bulks by DFT calculations - J. Chem. Sci. - X-MOL Platinum(II), palladium(II) and gold(I) benzimidazolin-2-ylidene as potential probes for determination of N-heterocyclic carbene donor strengths and steric bulks by DFT calculations - J. Chem. Sci. - X-MOL](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs12039-020-01785-2/MediaObjects/12039_2020_1785_Figa_HTML.png)
Platinum(II), palladium(II) and gold(I) benzimidazolin-2-ylidene as potential probes for determination of N-heterocyclic carbene donor strengths and steric bulks by DFT calculations - J. Chem. Sci. - X-MOL
![Computed ligand effects on the oxidative addition of phenyl halides to phosphine supported palladium(0) catalysts - Dalton Transactions (RSC Publishing) DOI:10.1039/C4DT01758G Computed ligand effects on the oxidative addition of phenyl halides to phosphine supported palladium(0) catalysts - Dalton Transactions (RSC Publishing) DOI:10.1039/C4DT01758G](https://pubs.rsc.org/image/article/2014/DT/c4dt01758g/c4dt01758g-s2_hi-res.gif)
Computed ligand effects on the oxidative addition of phenyl halides to phosphine supported palladium(0) catalysts - Dalton Transactions (RSC Publishing) DOI:10.1039/C4DT01758G
![Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs42004-020-0287-0/MediaObjects/42004_2020_287_Fig3_HTML.png)
Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry
![Palladium complexes of C/Se and N/E (E = Se, Te) ligands, 2-(3,5-dimethylpyrazol-1-yl)phenyl substituted chalcogeno-ethers: Functional group effect on structure and catalytic activity - ScienceDirect Palladium complexes of C/Se and N/E (E = Se, Te) ligands, 2-(3,5-dimethylpyrazol-1-yl)phenyl substituted chalcogeno-ethers: Functional group effect on structure and catalytic activity - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X15301571-fx1.jpg)
Palladium complexes of C/Se and N/E (E = Se, Te) ligands, 2-(3,5-dimethylpyrazol-1-yl)phenyl substituted chalcogeno-ethers: Functional group effect on structure and catalytic activity - ScienceDirect
![Solvent effects on ligand exchange between two different pd(II) organometallic complexes - ScienceDirect Solvent effects on ligand exchange between two different pd(II) organometallic complexes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0020169300922709-fx1.gif)