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51364-51-3 - Tris(dibenzylideneacetone)dipalladium(0), Pd 21.5% min - Bis[tris(dibenzylideneacetone)palladium(0)] - Pd<sub>2</sub>(dba)<sub>3</sub> - 12760 - Alfa Aesar

12760 Tris(dibenzylideneacetone)dipalladium(0), Pd 21.5% min

CAS Number
51364-51-3
Synonyms
Bis[tris(dibenzylideneacetone)palladium(0)]
Pd2(dba)3

Size Price ($) Quantity Availability
1g 65.70
5g 202.00
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Tris(dibenzylideneacetone)dipalladium(0), Pd 21.5% min

MDL
MFCD00013310

Chemical Properties

Formula
C51H42O3Pd2
Formula Weight
915.74
Form
Powder
Melting point
152-155°
Sensitivity
Air & Moisture Sensitive
Solubility
Soluble in chlorinated solvents, benzene and THF.

Applications

Tris(dibenzylideneacetone)dipalladium(0) is the most widely used Pd0 precursor complex in synthesis and catalysis, in particular as a catalyst for various coupling reactions. It is used as a catalyst precursor for palladium-catalyzed carbon-nitrogen bond formation, conversion of aryl chlorides, triflates and nonaflates to nitroaromatics. It is used as catalyst for the synthesis of epoxides, alpha-arylation of ketones, in combination with BINAP for the asymmetric heck arylation of olefins, site-selective benzylic sp3 palladium-catalyzed direct arylation and homoallylic diamination of terminal olefins. It also used for palladium-catalyzed one-pot synthesis of tricyclic indolines, in the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles and cross-coupling of aryl halides with aryl boronic acids.

Notes

Handle under nitrogen atmosphere and protect from moisture and air.

Literature References

Takahashi, Y.; Ito, Ts.; Sakai, S.; Ishii, Y. A novel palladium(0) complex; bis(dibenzylideneacetone)palladium(0). J. Chem. Soc. D 1970, 17, 1065-1066.

Franzen, S. Determination of the Solubility Limit of Tris(dibenzylideneacetone) dipalladium(0) in Tetrahydrofuran/Water Mixtures. J. Chem. Educ. 1970, 88, 619-623.

Other References

Harmonized Tariff Code
2843.90
TSCA
No

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