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  2. Tetrakis (triphenylphosphine)palladium (0) - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(triphenylphosphine...

    Pd(PPh 3) 4 is widely used as a catalyst for palladium-catalyzed coupling reactions. [7] 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 ...

  3. Tetrakis(triphenylphosphine)platinum(0) - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(triphenylphosphi...

    The reaction occurs in two distinct steps. In the first step, PtCl 2 (PPh 3) 2 is generated. In the second step, this platinum(II) complex is reduced. The overall synthesis can be summarized as: K 2 [PtCl 4] + 2KOH + 4PPh 3 + C 2 H 5 OH → Pt(PPh 3) 4 + 4KCl + CH 3 CHO + 2H 2 O. Pt(PPh 3) 4 reacts with oxidants to give platinum(II) derivatives:

  4. Metal-phosphine complex - Wikipedia

    en.wikipedia.org/wiki/Metal-phosphine_complex

    One of the first applications of phosphine ligands in catalysis was the use of triphenylphosphine in "Reppe" chemistry (1948), which included reactions of alkynes, carbon monoxide, and alcohols. [16] In his studies, Reppe discovered that this reaction more efficiently produced acrylic esters using NiBr 2 (PPh 3) 2 as a catalyst instead of NiBr 2.

  5. Palladium compounds - Wikipedia

    en.wikipedia.org/wiki/Palladium_compounds

    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.

  6. Suzuki reaction - Wikipedia

    en.wikipedia.org/wiki/Suzuki_reaction

    The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. [1] [2] [3] It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their contribution to the discovery and development of noble metal catalysis in organic ...

  7. Triphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine

    In the Appel reaction, a mixture of PPh 3 and CX 4 (X = Cl, Br) is used to convert alcohols to alkyl halides. Triphenylphosphine oxide (OPPh 3) is a byproduct. PPh 3 + CBr 4 + RCH 2 OH → OPPh 3 + RCH 2 Br + HCBr 3. This reaction commences with nucleophilic attack of PPh 3 on CBr 4, an extension of the quaternization reaction listed above.

  8. Oxidation state - Wikipedia

    en.wikipedia.org/wiki/Oxidation_state

    Fractional oxidation states are often used to represent the average oxidation state of several atoms of the same element in a structure. For example, the formula of magnetite is Fe 3 O 4, implying an average oxidation state for iron of + ⁠ 8 / 3 ⁠. [17]: 81–82 However, this average value may not be representative if the atoms are not ...

  9. Palladium(III) compounds - Wikipedia

    en.wikipedia.org/wiki/Palladium(III)_compounds

    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]