520659

Palladium(II) chloride

≥99.9%

• Szinonimák: Dichloropalladium, Palladium dichloride, Palladous chloride
• Tapasztalati képlet (Hill-képlet): Cl₂Pd
• CAS-szám: 7647-10-1
• Molekulatömeg: 177.33
• EC-szám: 231-596-2
• MDL-szám: MFCD00003558
• UNSPSC kód: 12161600
• PubChem Substance ID: 24874155
• NACRES: NA.22

Tulajdonságok

• Minőségi szint: 100
• Teszt: ≥99.9%
• összetétel: Pd, 59-60%
• reakcióalkalmasság: core: palladium; reaction type: Buchwald-Hartwig Cross Coupling Reaction; reaction type: Heck Reaction; reaction type: Hiyama Coupling; reaction type: Negishi Coupling; reaction type: Sonogashira Coupling; reaction type: Stille Coupling; reaction type: Suzuki-Miyaura Coupling; reagent type: catalyst
• mp: 678-680 °C (lit.)
• sűrűség: 4 g/mL at 25 °C (lit.)
• SMILES string: Cl[Pd]Cl
• InChI: 1S/2ClH.Pd/h2*1H;/q;;+2/p-2
• Nemzetközi kémiai azonosító kulcs: PIBWKRNGBLPSSY-UHFFFAOYSA-L

Leírás

Általános leírás

Palladium(II) chloride (PdCl₂) reacts with unsubstituted or alkyl-substituted cyclic ketones in the CO atmosphere to afford acyclic diesters and acyclic chloro-substituted monoesters. PdCl₂ reacts with N,N-dimethylallylamine in methanol to afford di-μ-chloro-bis(2-methoxy-3-N,N-dimethylaminopropyl)dipalladium(II). Palladium dichloride, acetate and acetylacetonate in the [bmim][BF₄] or [bmim][PF₆] (where[bmim]⁺ = 1-butyl-3-methylimidazolium cation) ionic liquids have been employed for the hydrodimerization of butadiene to form octa-2,7-dien-1-ol.

Palladium(II) chloride is used as an oxidizing agent and catalyst for the Suzuki-Miyaura and Mizoroki-Heck reactions.

Alkalmazás

Application Guide for Palladium Catalyzed Cross-Coupling Reactions

Used in the synthesis of semiconducting metal-containing polymers in which the polypyrrole backbone has a conformational energy minimum and is nearly planar.

Palladium(II) chloride (PdCl₂) was used in the following studies:

• As catalyst for the carbonylation of organic tellurides by reaction with carbon monoxide.
• As a catalyst along with Cu(II) for the deamination of phenethylamines to phenyl substituted pyrroles.
• Together with PEG 300, promoted efficient Suzuki-coupling of aryl chlorides with aryl boronic acids.

For small scale and high throughput uses, product is also available as ChemBeads (919853)

Biztonsági adatok

• Piktogramok: GHS05,GHS07,GHS09
• Figyelmeztetés: Danger
• Figyelmeztető mondatok: H290,H302,H317,H318,H410
• Óvintézkedésre vonatkozó mondatok: P234 - P273 - P280 - P301 + P312 - P302 + P352 - P305 + P351 + P338
• Veszélyességi osztályok: Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Met. Corr. 1 - Skin Sens. 1
• Tárolási osztály kódja: 8B - Non-combustible corrosive hazardous materials
• WGK: WGK 3
• Lobbanási pont (F): Not applicable
• Lobbanási pont (C): Not applicable
• Egyéni védőeszköz: Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges