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EnCat™ & Other Catalysts | Sigma-Aldrich
EnCat™ & Other Catalysts | Sigma-Aldrich

Palladium(II) Acetate, Recrystallized | Sigma-Aldrich
Palladium(II) Acetate, Recrystallized | Sigma-Aldrich

PhosphonicS™ SPM3Pd | Palladium acetate 3-mercaptopropyl ethyl sulfide Silica | Sigma-Aldrich
PhosphonicS™ SPM3Pd | Palladium acetate 3-mercaptopropyl ethyl sulfide Silica | Sigma-Aldrich

Improved ethanol electrooxidation performance by shortening Pd–Ni active site distance in Pd–Ni–P nanocatalysts | Nature Communications
Improved ethanol electrooxidation performance by shortening Pd–Ni active site distance in Pd–Ni–P nanocatalysts | Nature Communications

Pd(II) EnCat® BINAP30 | Sigma-Aldrich | Sigma-Aldrich
Pd(II) EnCat® BINAP30 | Sigma-Aldrich | Sigma-Aldrich

Synthesis and Characterization of Palladium Supported Amino Functionalized Magnetic-MOF-MIL-101 as an Efficient and Recoverable Catalyst for Mizoroki–Heck Cross-Coupling | SpringerLink
Synthesis and Characterization of Palladium Supported Amino Functionalized Magnetic-MOF-MIL-101 as an Efficient and Recoverable Catalyst for Mizoroki–Heck Cross-Coupling | SpringerLink

Palladium(II) acetylacetonate 99 % | 14024-61-4 | Sigma-Aldrich
Palladium(II) acetylacetonate 99 % | 14024-61-4 | Sigma-Aldrich

Synthesis and Characterization of Palladium Supported Amino Functionalized Magnetic-MOF-MIL-101 as an Efficient and Recoverable Catalyst for Mizoroki–Heck Cross-Coupling | SpringerLink
Synthesis and Characterization of Palladium Supported Amino Functionalized Magnetic-MOF-MIL-101 as an Efficient and Recoverable Catalyst for Mizoroki–Heck Cross-Coupling | SpringerLink

3375-31-3|Palladium(II) acetate|Sigma Aldrich|Pd(OAc)2|(acetyloxy)palladio acetate
3375-31-3|Palladium(II) acetate|Sigma Aldrich|Pd(OAc)2|(acetyloxy)palladio acetate

Small palladium islands embedded in palladium–tungsten bimetallic nanoparticles form catalytic hotspots for oxygen reduction | Nature Communications
Small palladium islands embedded in palladium–tungsten bimetallic nanoparticles form catalytic hotspots for oxygen reduction | Nature Communications

Palladium(II) acetate 99.9+ % trace metals | 3375-31-3 | Sigma-Aldrich
Palladium(II) acetate 99.9+ % trace metals | 3375-31-3 | Sigma-Aldrich

Palladium(II) acetate 99.9+ % trace metals | 3375-31-3 | Sigma-Aldrich
Palladium(II) acetate 99.9+ % trace metals | 3375-31-3 | Sigma-Aldrich

PDF) Pd Supported IRMOF-3: Heterogeneous, Efficient and Reusable Catalyst for Heck Reaction
PDF) Pd Supported IRMOF-3: Heterogeneous, Efficient and Reusable Catalyst for Heck Reaction

Supported Palladium Nanoparticles Synthesized by Living Plants as a Catalyst for Suzuki-Miyaura Reactions
Supported Palladium Nanoparticles Synthesized by Living Plants as a Catalyst for Suzuki-Miyaura Reactions

Palladium(II) acetate, recrystallized 97 % | 3375-31-3 | Sigma-Aldrich
Palladium(II) acetate, recrystallized 97 % | 3375-31-3 | Sigma-Aldrich

Palladium(II) Acetate
Palladium(II) Acetate

Bis(triphenylphosphine)palladium(II) diacetate 98 % | 14588-08-0 | Sigma-Aldrich
Bis(triphenylphosphine)palladium(II) diacetate 98 % | 14588-08-0 | Sigma-Aldrich

Palladium(II) acetate | C4H6O4Pd | ChemSpider
Palladium(II) acetate | C4H6O4Pd | ChemSpider

Heterogeneous versus Homogeneous Palladium Catalysts for Cross‐Coupling Reactions - Pagliaro - 2012 - ChemCatChem - Wiley Online Library
Heterogeneous versus Homogeneous Palladium Catalysts for Cross‐Coupling Reactions - Pagliaro - 2012 - ChemCatChem - Wiley Online Library

From small molecules to polymeric catalysts in the oscillatory carbonylation reaction: multiple effects of adding HI - Physical Chemistry Chemical Physics (RSC Publishing)
From small molecules to polymeric catalysts in the oscillatory carbonylation reaction: multiple effects of adding HI - Physical Chemistry Chemical Physics (RSC Publishing)

β-Diketimine appended periodic mesoporous organosilica as a scaffold for immobilization of palladium acetate: An efficient green catalyst for Wacker type reaction - ScienceDirect
β-Diketimine appended periodic mesoporous organosilica as a scaffold for immobilization of palladium acetate: An efficient green catalyst for Wacker type reaction - ScienceDirect

Palladium(II) acetylacetonate 99 % | 14024-61-4 | Sigma-Aldrich
Palladium(II) acetylacetonate 99 % | 14024-61-4 | Sigma-Aldrich

1,2-Bis(phenylsulfinyl)ethane palladium(II) acetate | 858971-43-4 | Sigma-Aldrich
1,2-Bis(phenylsulfinyl)ethane palladium(II) acetate | 858971-43-4 | Sigma-Aldrich

trans-Bis(dicyclohexylamine)palladium(II) acetate | 628339-96-8 | Sigma-Aldrich
trans-Bis(dicyclohexylamine)palladium(II) acetate | 628339-96-8 | Sigma-Aldrich

Catalysts | Free Full-Text | Synthesis, Structure, and Catalytic Reactivity of Pd(II) Complexes of Proline and Proline Homologs | HTML
Catalysts | Free Full-Text | Synthesis, Structure, and Catalytic Reactivity of Pd(II) Complexes of Proline and Proline Homologs | HTML

Palladium(II) acetate 99.9+ % trace metals | 3375-31-3 | Sigma-Aldrich
Palladium(II) acetate 99.9+ % trace metals | 3375-31-3 | Sigma-Aldrich

Switching on palladium catalyst electrochemical removal from a palladium acetate–acetonitrile system via trace water addition - Green Chemistry (RSC Publishing)
Switching on palladium catalyst electrochemical removal from a palladium acetate–acetonitrile system via trace water addition - Green Chemistry (RSC Publishing)

Supported Palladium Nanoparticles Synthesized by Living Plants as a Catalyst for Suzuki-Miyaura Reactions
Supported Palladium Nanoparticles Synthesized by Living Plants as a Catalyst for Suzuki-Miyaura Reactions