216666

Tetrakis(triphenylphosphine)palladium(0)

99%

• Szinonimák: Palladium-tetrakis(triphenylphosphine), Pd(PPh₃)₄
• Lineáris képlet: Pd[(C₆H₅)₃P]₄
• CAS-szám: 14221-01-3
• Molekulatömeg: 1155.56
• Beilstein: 6704828
• EC-szám: 238-086-9
• MDL-szám: MFCD00010012
• UNSPSC kód: 12352103
• PubChem Substance ID: 24852971
• NACRES: NA.22

Tulajdonságok

• Minőségi szint: 200
• Teszt: 99%
• form: solid
• reakcióalkalmasság: core: palladium; reaction type: Cross Couplings; 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; reaction type: Buchwald-Hartwig Cross Coupling Reaction
• parameter: air sensitive
• tárolási hőmérséklet: 2-8°C
• SMILES string: [Pd].c1ccc(cc1)P(c2ccccc2)c3ccccc3.c4ccc(cc4)P(c5ccccc5)c6ccccc6.c7ccc(cc7)P(c8ccccc8)c9ccccc9.c%10ccc(cc%10)P(c%11ccccc%11)c%12ccccc%12
• InChI: 1S/4C18H15P.Pd/c4*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;/h4*1-15H;
• Nemzetközi kémiai azonosító kulcs: NFHFRUOZVGFOOS-UHFFFAOYSA-N

Leírás

Általános leírás

Palladium-tetrakis(triphenylphosphine) (Pd(PPh₃)₄) iscoordination complex of palladium and is widely used palladium cross-coupling catalyst. These applications include Negishi coupling, Suzuki coupling, Stille coupling, Sonogashira coupling, and Buchwald-Hartwig amination reactions.




Tetrakis(triphenylphosphine)palladium(0) (Pd(PPh₃)₄) is a commonly used palladium(0) complex in chemical synthesis. It plays a vital role as a catalyst in various organic reactions, especially C-C, C-N, C-O, and C-heteroatom cross-coupling reactions. Pd(PPh₃)₄ finds extensive application in carbon-carbon bond-forming reactions such as the famous Heck, Suzuki-Miyaura, and Stille reactions. These reactions involve the coupling of aryl, alkyl, or vinyl halides with other organic compounds to yield valuable products. The catalytic cycle involves the oxidative addition of the organic halide to palladium(0), transmetalation with a suitable organometallic reagent or boronic acid, and reductive elimination to form the desired product. Pd(PPh₃)₄ has also been utilized in various other transformations including allylic substitutions, nucleophilic additions to alkenes and alkynes, and cycloadditions.

Alkalmazás

Application Guide for Palladium Catalyzed Cross-Coupling Reactions

Tetrakis(triphenylphosphine)palladium(0) can be used as a catalyst in:

• Negishi coupling (eq. 1), Suzuki coupling (eq. 2), Stille coupling (eq. 3), Sonogashira coupling reaction (eq. 4), and Buchwald-Hartwig amination reaction (eq. 5)
• The carbonylation of vinyl iodides (eq. 6)
• The reduction reaction of aryl bromides (eq. 7)
• Carbon-tin bond formation (eq. 8)

Biztonsági adatok

• Piktogramok: GHS07
• Figyelmeztetés: Warning
• Figyelmeztető mondatok: H302
• Óvintézkedésre vonatkozó mondatok: P264 - P270 - P301 + P312 - P501
• Veszélyességi osztályok: Acute Tox. 4 Oral
• Tárolási osztály kódja: 11 - Combustible Solids
• WGK: WGK 3
• Lobbanási pont (F): Not applicable
• Lobbanási pont (C): Not applicable
• Egyéni védőeszköz: Eyeshields, Gloves, type N95 (US)