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In chemistry, compounds of palladium(III) feature the noble metal palladium in the unusual +3 oxidation state (in most of its compounds, palladium has the oxidation state II). Compounds of Pd(III) occur in mononuclear and dinuclear forms. Palladium(III) is most often invoked, not observed in mechanistic organometallic chemistry. [1] [2]
Palladium is also used in electronics, dentistry, medicine, hydrogen purification, chemical applications, groundwater treatment, and jewelry. Palladium is a key component of fuel cells, in which hydrogen and oxygen react to produce electricity, heat, and water. Ore deposits of palladium and other PGMs are rare.
Thus element 164 with 7d 10 9s 0 is noted by Fricke et al. to be analogous to palladium with 4d 10 5s 0, and they consider elements 157–172 to have chemical analogies to groups 3–18 (though they are ambivalent on whether elements 165 and 166 are more like group 1 and 2 elements or more like group 11 and 12 elements, respectively). Thus ...
A similar palladium cycle but with different scenes and actors is observed in the Wacker process. Heck Reaction Mechanism This cycle is not limited to vinyl compounds, in the Sonogashira coupling one of the reactants is an alkyne and in the Suzuki coupling the alkene is replaced by an aryl boronic acid and in the Stille reaction by an aryl ...
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Palladium forms a variety of ionic, coordination, and organopalladium compounds, typically with oxidation state Pd 0 or Pd 2+. Palladium(III) compounds have also been reported. Palladium compounds are frequently used as catalysts in cross-coupling reactions such as the Sonogashira coupling and Suzuki reaction.
Catalysts are often based on palladium, which is frequently selected due to high functional group tolerance. Organopalladium compounds are generally stable towards water and air. Palladium catalysts can be problematic for the pharmaceutical industry, which faces extensive regulation regarding heavy metals.
Another commonly used palladium source is [Pd(PPh 3) 2 Cl 2], but complexes containing bidentate phosphine ligands, such as [PdCl 2], [PdCl 2], and [Pd(dppf)Cl 2] have also been used. [9] The drawback to such catalysts is the need for high loadings of palladium (up to 5 mol %), along with a larger amount of a copper co-catalyst. [9]