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Bis(2,4-pentanedionato-O,O')palladium(II)

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Bis(2,4-pentanedionato-O,O')palladium(II) Basic information

Product Name:
Bis(2,4-pentanedionato-O,O')palladium(II)
Synonyms:
  • ACETYLACETONE, PALLADIUM(II) DERIVATIVE
  • ACETYLACETONE PALLADIUM(II) SALT
  • Palladium acetylacetonate or Palladium(II)2,4-pentanedionate
  • Bis(acetylacetonato)palladium(II) dec. 205 halide free source of Pd
  • bis(2,4-pentanedionato-o,o')palladium(ii)
  • BIS(2,4-PENTANEDIONATO)PALLADIUM(II)
  • BIS(ACETYLACETONATO)PALLADIUM(II)
  • Bis(2,4-pentanedionato-O,O')palladium(II),99%
CAS:
14024-61-4
MF:
C10H14O4Pd
MW:
304.64
EINECS:
237-859-8
Product Categories:
  • metal beta-diketonate complexes
  • Catalysts for Organic Synthesis
  • Classes of Metal Compounds
  • Homogeneous Catalysts
  • Metal Complexes
  • Pd (Palladium) Compounds
  • Synthetic Organic Chemistry
  • Transition Metal Compounds
  • chemical reaction,pharm,electronic,materials
  • Pd
Mol File:
14024-61-4.mol
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Bis(2,4-pentanedionato-O,O')palladium(II) Chemical Properties

Melting point:
190 °C
vapor pressure 
0Pa at 25℃
storage temp. 
Store below +30°C.
solubility 
Soluble in benzene and chloroform.
form 
Solution
color 
Yellow to orange
Specific Gravity
1.862
Water Solubility 
INSOLUBLE
Hydrolytic Sensitivity
4: no reaction with water under neutral conditions
BRN 
4136188
InChI
InChI=1S/2C5H8O2.Pd/c2*1-4(6)3-5(2)7;/h2*3,6H,1-2H3;/q;;+2/p-2/b2*4-3-;
InChIKey
RJJXYEQOOACRKP-LNKPDPKZSA-M
SMILES
O([Pd]O/C(/C)=C\C(=O)C)/C(/C)=C\C(=O)C
LogP
2.6 at 25℃
NIST Chemistry Reference
Bis(acetylacetonato)palladium(14024-61-4)
EPA Substance Registry System
Palladium, bis(2,4-pentanedionato-.kappa.O,.kappa.O')-, (SP-4-1)- (14024-61-4)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36-36/37/38-22
Safety Statements 
26-37/39
RIDADR 
3181
WGK Germany 
2
TSCA 
Yes
HS Code 
28439090

MSDS

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Bis(2,4-pentanedionato-O,O')palladium(II) Usage And Synthesis

Chemical Properties

yellow orange needles

Uses

Palladium(II) Acetylacetonate is an active anticancer agent. Exhibits growth inhibitory effect more than cisplatin in several cancer cells and treatment with Palladium(II) Acetylacetonate inhibits H460 cells. Palladium(II) Acetylacetonate is a catalyst for various organic transformations.

Uses

Palladium(II) acetylacetonate (Pd(acac)2) was used in the following studies:

  • Typical high-temperature organic solution phase protocol for the preparation of monodisperse CuPd alloy nanoparticles (NPs).
  • Preparation of [(NHC)Pd(acac)L] (where L=Me, NHC = N-heterocyclic carbene) complexes. These complexes efficiently catalyze the Heck reaction of activated aryl bromides.
  • As catalyst in the decarboxylative cross-coupling of arylcarboxylic acids with aryl halides.

General Description

Palladium(II) acetylacetonate (Pd(acac)2) is a metal-organic complex. Sublimation of Pd(acac)2 has been investigated by thermogravimetry and XRD. The temperature range for the sublimation of Pd(acac)2, without undergoing thermal decomposition, was determined to be 100-160°C in the presence of inert gas helium.

Flammability and Explosibility

Highly flammable

Purification Methods

It can be recrystallised from *C6H6/pet ether and sublimes in vacuo. It is soluble in heptane, *C6H6 (1.2% at 20o, 2.2 at 40o), toluene (0.56% at 20o, 1.4% at 40o) and acetylacetone (1.2% at 20o, 0.05% at 40o). [West & Riley J Inorg Nucl Chem 5 295 1957/8, Fernelius & Bryant Inorg Synth V 105 1957, Beilstein 1 IV 3676.]

Bis(2,4-pentanedionato-O,O')palladium(II) Preparation Products And Raw materials

Raw materials

Bis(2,4-pentanedionato-O,O')palladium(II)Supplier

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