Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
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.
^Cite error: The named reference structure was invoked but never defined (see the help page).
^Tatsuno, Y.; Yoshida, T.; Otsuka, S. "(η3-allyl)palladium(II) Complexes" Inorganic Syntheses, 1990, volume 28, pages 342-345. ISBN 0-471-52619-3
and 8 Related for: Allylpalladium chloride dimer information
Allylpalladium(II) chloridedimer (APC) is a chemical compound with the formula [(η3-C3H5)PdCl]2. This yellow air-stable compound is an important catalyst...
to palladium(0) to give allylpalladiumchloridedimer, (C3H5)2Pd2Cl2. Dehydrohalogenation gives cyclopropene. Allyl chloride is highly toxic and flammable...
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including natural rubber. Transition-metal allyl complexes, such as allylpalladiumchloridedimer Wikiquote has quotations related to Allyl group. Allylic strain...
aromatic decarboxylation: The iconic complex in this series is allylpalladiumchloridedimer (APC). Allyl compounds with suitable leaving groups react with...
2010 using aryl halides, (trifluoromethyl)triethylsilane and allylpalladiumchloridedimer In radical trifluoromethylation the active species is the trifluoromethyl...
example, Zeise's salt), and η3-allyl compounds (for example, allylpalladiumchloridedimer); metallocenes containing cyclopentadienyl ligands (for example...