Product Information:
palladium acetate(3375-31-3)
Palladium acetate(3375-31-3) is a catalyst for many organic reactions by combining with many common
classes of organic compounds such as alkenes, dienes, and alkyl, aryl, and vinyl halides to form reactive adducts. Alkenes and π-allyl coordination to palladium(II) acetate involves sigma-type donation from the pi orbital of the alkene or π-allyl with concomitant pi-backbonding into an empty pi* orbital on the alkene or π-allyl. The greater the sigma donation to the metal is, the greater the pi-backbonding. The greater the pi-backbonding is, the greater the reduction in the bond order of the alkene or π-allyl.Reduction of the alkenes or π-allyl by coordination to palladium(II) acetate reverses the reactivity of the organic ligand allowing them to undergo reactions with nucleophiles rather than electrophiles.
| Product name: | palladium acetate |
| Other name: | hexakis(acetato)tripalladium; bis(acetato)palladium; Palladiumacetatemingoldbrownxtl; Acetic acid palladium(II) salt; Palladium(II)acetat; Palladousacetate; palladium - acetic acid (1:2); acetate, palladium(2+) salt (1:1) |
| Appearance | Reddish brown crystalline powder |
| Assay(Pd) | 47% |
| Purity: | 99% |
| Molecular Formula: | Pd(C2H3O2)2 |
| Formula Weight: | 224.49 |
| CAS No.: | 3375-31-3 |
| Solubility: | Insoluble in water Soluble in benzene, toluene and acetic acid. Slowly decomposited in ethanol solution. |
| Density | 4.352 |
| Main function: | chemical catalyst |
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Product Categories : API Powder > Monobenzone
classes of organic compounds such as alkenes, dienes, and alkyl, aryl, and vinyl halides to form reactive adducts. Alkenes and π-allyl coordination to palladium(II) acetate involves sigma-type donation from the pi orbital of the alkene or π-allyl with concomitant pi-backbonding into an empty pi* orbital on the alkene or π-allyl. The greater the sigma donation to the metal is, the greater the pi-backbonding. The greater the pi-backbonding is, the greater the reduction in the bond order of the alkene or π-allyl.Reduction of the alkenes or π-allyl by coordination to palladium(II) acetate reverses the reactivity of the organic ligand allowing them to undergo reactions with nucleophiles rather than electrophiles.
