From Wikipedia, the free encyclopedia
Jump to navigation Jump to search
3D model of the tetrakis(triphenylphosphine)palladium(0) molecule
IUPAC name
Other names
TPP palladium(0)
3D model (JSmol)
ECHA InfoCard 100.034.609
RTECS number Unregistered
Molar mass 1,155.59 g·mol−1
Appearance Bright yellow crystals
Melting point decomposes around 115 °C
four triphenylphosphine monodentate
ligands attached to a central Pd(0)
atom in a tetrahedral geometry
0 D
R-phrases (outdated) n/a
S-phrases (outdated) S22, S24/25
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oilHealth code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroformReactivity (yellow): no hazard codeSpecial hazards (white): no codeNFPA 704 four-colored diamond
Related compounds
Related complexes
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☑Y verify (what is ☑Y☒N ?)
Infobox references

Tetrakis(triphenylphosphine)palladium(0) (sometimes called quatrotriphenylphosphine) is the chemical compound Pd[P(C6H5)3]4, often abbreviated Pd(PPh3)4, or rarely PdP4. It is a bright yellow crystalline solid that becomes brown upon decomposition in air.

Structure and properties[edit]

The four phosphorus atoms are at the corners of a tetrahedron surrounding the palladium(0) center. This structure is typical for four-coordinate 18 e complexes.[1] The corresponding complexes Ni(PPh3)4 and Pt(PPh3)4 are also well known. Such complexes reversibly dissociate PPh3 ligands in solution, so reactions attributed to Pd(PPh3)4 often in fact arise from Pd(PPh3)3 or even Pd(PPh3)2.


Tetrakis(triphenylphosphine)palladium(0) was first prepared by Lamberto Malatesta et al. in the 1950s by reduction of sodium chloropalladate with hydrazine in the presence of the phosphine.[2] It is commercially available, but can be prepared in two steps from Pd(II) precursors:

PdCl2 + 2 PPh3 → PdCl2(PPh3)2
PdCl2(PPh3)2 + 2 PPh3 + ​52 N2H4 → Pd(PPh3)4 + ​12 N2 + 2 N2H5Cl

Both steps may be carried out in a one-pot reaction, without isolating and purifying the PdCl2(PPh3)2 intermediate.[3] Reductants other than hydrazine can be employed. The compound is sensitive to air, but can be purified by washing with methanol to give the desired yellow powder. It is usually stored cold under argon.


Pd(PPh3)4 is widely used as a catalyst for palladium-catalyzed coupling reactions.[4] Prominent applications include the Heck reaction, Suzuki coupling, Stille coupling, Sonogashira coupling, and Negishi coupling. These processes begin with two successive ligand dissociations followed by the oxidative addition of an aryl halide to the Pd(0) center:

Pd(PPh3)4 + ArBr → PdBr(Ar)(PPh3)2 + 2 PPh3


  1. ^ Elschenbroich, C.; Salzer, A. (1992). Organometallics: A Concise Introduction (2nd ed.). Weinheim: Wiley-VCH. ISBN 3-527-28165-7.
  2. ^ Malatesta, L.; Angoletta, M. (1957). "Palladium(0) compounds. Part II. Compounds with triarylphosphines, triaryl phosphites, and triarylarsines". J. Chem. Soc. 1957: 1186. doi:10.1039/JR9570001186.
  3. ^ Coulson, D. R.; Satek, L. C.; Grim, S. O. (1972). "Tetrakis(triphenylphosphine)palladium(0)". Inorg. Synth. Inorganic Syntheses. 13: 121. doi:10.1002/9780470132449.ch23. ISBN 978-0-470-13244-9.
  4. ^ Van Leeuwen, P. W. (2005). Homogeneous Catalysis: Understanding the Art. Springer. ISBN 1-4020-3176-9.