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Allylpalladium chloride dimer information


Allylpalladium(II) chloride dimer
Names
IUPAC name
Allylpalladium(II) chloride dimer
Other names
Allylpalladium chloride dimer
bis(allyl)di-μ-chloro-dipalladium(II)
APC
Identifiers
CAS Number
  • 12012-95-2 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 21171401 checkY
ECHA InfoCard 100.031.423 Edit this at Wikidata
EC Number
  • 234-579-8
PubChem CID
  • 61538
CompTox Dashboard (EPA)
  • DTXSID10897423
InChI
  • InChI=1S/2C3H5.2ClH.2Pd/c2*1-3-2;;;;/h2*3H,1-2H2;2*1H;;/q;;;;2*+1/p-2 checkY
    Key: TWKVUTXHANJYGH-UHFFFAOYSA-L checkY
  • InChI=1/2C3H5.2ClH.2Pd/c2*1-3-2;;;;/h2*3H,1-2H2;2*1H;;/q;;;;2*+1/p-2/r2C3H5ClPd/c2*1-2-3-5-4/h2*2H,1,3H2
    Key: TWKVUTXHANJYGH-NNVIZEFPAF
SMILES
  • Cl[Pd]CC=C.C=CC[Pd]Cl
Properties
Chemical formula
C6H10Cl2Pd2
Molar mass 365.85 g/mol
Appearance Pale yellow, crystalline solid
Melting point decomp at 155-156 °C
Solubility in water
Insoluble
Solubility in other solvents Chloroform
benzene
acetone
methanol
Structure[1]
Crystal structure
monoclinic
Space group
P21/n, No. 14
Formula units (Z)
2
Hazards
GHS labelling:
Pictograms
GHS07: Exclamation mark
Signal word
Warning
Hazard statements
H302, H312, H315, H319, H332, H335
Precautionary statements
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501
Safety data sheet (SDS) http://www.colonialmetals.com/pdf/5048.pdf
Related compounds
Related compounds
3-allyl)(η5 – cyclopentadienyl)palladium(II)
di-μ-chlorobis(crotyl)dipalladium
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Allylpalladium(II) chloride dimer (APC) is a chemical compound with the formula [(η3-C3H5)PdCl]2. This yellow air-stable compound is an important catalyst used in organic synthesis.[2] It is one of the most widely used transition metal allyl complexes.

  1. ^ Cite error: The named reference structure was invoked but never defined (see the help page).
  2. ^ Tatsuno, Y.; Yoshida, T.; Otsuka, S. "(η3-allyl)palladium(II) Complexes" Inorganic Syntheses, 1990, volume 28, pages 342-345. ISBN 0-471-52619-3

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Allylpalladium chloride dimer

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Allylpalladium(II) chloride dimer (APC) is a chemical compound with the formula [(η3-C3H5)PdCl]2. This yellow air-stable compound is an important catalyst...

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Allyl chloride

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to palladium(0) to give allylpalladium chloride dimer, (C3H5)2Pd2Cl2. Dehydrohalogenation gives cyclopropene. Allyl chloride is highly toxic and flammable...

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APC

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a protein from the light-harvesting phycobiliprotein family Allylpalladium chloride dimer, a chemical compound Ammonium perchlorate, a powerful oxidizer...

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Allyl group

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including natural rubber. Transition-metal allyl complexes, such as allylpalladium chloride dimer Wikiquote has quotations related to Allyl group. Allylic strain...

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Organopalladium chemistry

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aromatic decarboxylation: The iconic complex in this series is allylpalladium chloride dimer (APC). Allyl compounds with suitable leaving groups react with...

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Trifluoromethylation

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2010 using aryl halides, (trifluoromethyl)triethylsilane and allylpalladium chloride dimer In radical trifluoromethylation the active species is the trifluoromethyl...

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Carbon

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example, Zeise's salt), and η3-allyl compounds (for example, allylpalladium chloride dimer); metallocenes containing cyclopentadienyl ligands (for example...

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Cyclopentadienyl allyl palladium

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allyl ligands. This complex is produced by the reaction of allylpalladium chloride dimer with sodium cyclopentadienide: 2 C5H5Na + (C3H5)2Pd2Cl2 → 2...

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