Bis(triphenylphosphine)palladium chloride

From Wikipedia, the free encyclopedia
Bis(triphenylphosphine)palladium chloride
Trans-dichlorobis(triphenylphosphine)palladium(II)-2D.png
Trans-dichlorobis(triphenylphosphine)palladium(II)-from-xtal-3D-balls.png
Dichlorobis(triphenylphosphine)palladium(II).jpg
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.034.299 Edit this at Wikidata
  • InChI=1S/2C18H15P.2ClH.Pd/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h2*1-15H;2*1H;/q;;;;+2/p-2 checkY
    Key: YNHIGQDRGKUECZ-UHFFFAOYSA-L checkY
  • InChI=1/2C18H15P.2ClH.Pd/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h2*1-15H;2*1H;/q;;;;+2/p-2
    Key: YNHIGQDRGKUECZ-NUQVWONBAO
  • ionic form: [Pd+2].[Cl-].[Cl-].c3c(P(c1ccccc1)c2ccccc2)cccc3.c1ccccc1P(c2ccccc2)c3ccccc3
  • coordination form: Cl[Pd-2](Cl)([P+](c0ccccc0)(c0ccccc0)(c0ccccc0))[P+](c0ccccc0)(c0ccccc0)(c0ccccc0)
Properties
C36H30Cl2P2Pd
Molar mass 701.90 g·mol−1
Appearance yellow powder
Melting point 260°C (decomposed around 300°C)
Insoluble in water, acetone, ether, Carbon tetrachloride and n-heptane // Soluble in CHCl3 and CH2Cl2, Chloroform (Slightly), Methanol (Slightly, Heated)
Hazards
NFPA 704 (fire diamond)
2
1
0
Flash point 181.7°C
Related compounds
Related compounds
 Bis(triphenylphosphine)platinum chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY  (what is checkY☒N ?)
Infobox references

Bis(triphenylphosphine)palladium chloride is a coordination compound of palladium containing two triphenylphosphine and two chloride ligands. It is a yellow solid that is soluble in some organic solvents. It is used for palladium-catalyzed coupling reactions, e.g. the Sonogashira–Hagihara reaction. The complex is square planar. Many analogous complexes are known with different phosphine ligands.

Preparation and reactions[]

This compound may be prepared by treating palladium(II) chloride with triphenylphosphine:[1][2]

PdCl2 + 2 PPh3 → PdCl2(PPh3)2

Upon reduction with hydrazine in the presence of excess triphenylphosphine, the complex is a precursor to tetrakis(triphenylphosphine)palladium, Pd(PPh3)4:[3]

2 PdCl2(PPh3)2 + 4 PPh3 + 5 N2H4 → 2 Pd(PPh3)4 + N2 + 4 N2H5+Cl−

Structure[]

Several crystal structures containing PdCl2(PPh3)2 have been reported. In all of the structures, PdCl2(PPh3)2 adopts a square planar coordination geometry and the trans isomeric form.[4][5][6][7]

Applications[]

The complex is used as a pre-catalyst for a variety of coupling reactions.[8]

One-pot Procedure for the Synthesis of Unsymmetrical Diarylalkynes.

The Suzuki reaction was once limited by high levels of catalyst and the limited availability of boronic acids. Replacements for halides were also found, increasing the number of coupling partners for the halide or pseudohalide as well. Using bis(triphenylphosphine)palladium chloride as the catalyst, triflates and boronic acids have been coupled on an 80 kilogram scale in good yield.[9] The same catalyst is effective for the Sonogashira coupling.[10]

See also[]

References[]

  1. ^ Norio Miyaura and Akira Suzuki (1990). "Palladium-Catalyzed Reaction of 1-Alkenylboronates with Vinylic Halides: (1Z,3E)-1-Phenyl-1,3-octadiene". Organic Syntheses. 68: 130. doi:10.15227/orgsyn.068.0130.CS1 maint: uses authors parameter (link)
  2. ^ Hiroshi Itatani, J.C.Bailar (1967). "Homogeneous Catalysis in the Reactions of olefinic Substances. V.Hydrogenation of Soybean Oil Methyl Ester with Triphenylphosphine and Triphenylarsine Palladium Catalysts". Journal of the American Oil Chemists' Society. 44: 147. doi:10.1007/BF02558176. S2CID 93580917.CS1 maint: uses authors parameter (link)
  3. ^ D. R. Coulson (1972). "Tetrakis(triphenylphosphine)palladium(0)". Inorganic Syntheses. Inorg. Synth. Inorganic Syntheses. 13. pp. 121–124. doi:10.1002/9780470132449.ch23. ISBN 9780470132449.
  4. ^ G. Ferguson, R. McCrindle, A. J. McAlees and M. Parvez (1982). "trans-Dichlorobis(triphenylphosphine)palladium(II)". Acta Crystallogr. B38 (10): 2679–2681. doi:10.1107/S0567740882009583.CS1 maint: uses authors parameter (link)
  5. ^ G. Steyl (2006). "trans-Dichlorobis(triphenylphosphine)palladium(II) dichloromethane solvate". Acta Crystallogr. E. 62 (6): m1324–m1325. doi:10.1107/S1600536806017521.
  6. ^ J. Pons, J. García-Antón, X. Solans, M. Font-Bardia, J. Ros (2008). "trans-Dichloridobis(triphenylphosphine)palladium(II)". Acta Crystallogr. E. 64 (Pt 5): m621. doi:10.1107/S1600536808008337. PMC 2961313. PMID 21202176.CS1 maint: uses authors parameter (link)
  7. ^ A. Naghipour, A. Ghorbani-Choghamarani, H. Babaee, M. Hashemi, B. Notash (2017). "Crystal structure of a novel polymorph of trans-dichlorobis (triphenylphosphine) palladium (II) and its application as a novel, efficient and retrievable catalyst for the amination of aryl halides and stille cross-coupling reactions". J. Organomet. Chem. 841: 31–38. doi:10.1016/j.jorganchem.2016.10.002.CS1 maint: uses authors parameter (link)
  8. ^ René Severin, Jessica Reimer, Sven Doye (2010). "One-Pot Procedure for the Synthesis of Unsymmetrical Diarylalkynes". J. Org. Chem. 75 (10): 3518–352. doi:10.1021/jo100460v. PMID 20420397.CS1 maint: uses authors parameter (link)
  9. ^ Jacks, T. E.; Belmont, Daniel T.; Briggs, Christopher A.; Horne, Nicole M.; Kanter, Gerald D.; Karrick, Greg L.; Krikke, James J.; McCabe, Richard J.; Mustakis; Nanninga, Thomas N. (2004). "Development of a Scalable Process for CI-1034, an Endothelin Antagonist". Organic Process Research & Development. 8 (2): 201–212. doi:10.1021/op034104g.CS1 maint: uses authors parameter (link)
  10. ^ Chinchilla, R.; Nájera, C. (2007). "The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry". Chem. Rev. 107 (3): 874–922. doi:10.1021/cr050992x. PMID 17305399.CS1 maint: uses authors parameter (link)
Retrieved from ""