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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Cyclopalladated complexes containing 2-C6R4PPh2 ligands (R = H, F): one-electron electrochemical reduction leading to metal-carbon sigma-bond cleavage via palladium(I)
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Cyclopalladated complexes containing 2-C6R4PPh2 ligands (R = H, F): one-electron electrochemical reduction leading to metal-carbon sigma-bond cleavage via palladium(I)

机译:含2-C6R4PPh2配体的环钯配合物(R = H,F):单电子电化学还原导致金属-碳σ键通过钯(I)裂解

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摘要

Three new ortho-metallated palladium complexes, [Pd(O,O' - hfacac)(kappa(2)-2-C6F4PPh2)] (11), [Pd-2(O,O'hfacac) (2)(mu-2-C6F4PPh2)(2)] (12) and [Pd(O,O' - hfacac)(kappa C-2-C6F4PPh2)(PPh3)] (13) (hfacac = hexafluoroacetylacetonate), have been prepared and fully characterised. The electrochemical reductions of complexes 11-13, together with those of other cyclopalladated complexes containing 2-C6R4PPh2 ligands (R = H, F) were studied by cyclic, rotating disk and microelectrode voltammetry. Evidence for the one-electron reduction of [PdI(kappa(2)-2-C6F4PPh2)(PPh(2)Fc)] (6) was obtained from coulometric analysis, although the product is unstable and undergoes further chemical processes. Preparative electro-reduction of [Pd-2(mu-Br)(2)(kappa(2)-2-C6F4PPh2)(2)] (7) in CH2Cl2 causes reductive cleavage of its Pd-C sigma-bonds and formation of the complex [PdBr2{PPh2(2-C6F4H)}(2)] (14); possible mechanisms are discussed.
机译:三种新的邻位金属钯配合物[Pd(O,O'-hfacac)(kappa(2)-2-C6F4PPh2)](11),[Pd-2(O,O'hfacac)(2)(mu- 2-C6F4PPh2)(2)](12)和[Pd(O,O'-hfacac)(κC-2-C6F4PPh2)(PPh3)](13)(hfacac =六氟乙酰丙酮)已经制备并充分表征。通过循环,转盘和微电极伏安法研究了配合物11-13的电化学还原反应,以及其他含有2-C6R4PPh2配体(R = H,F)的环钯配合物的电化学还原反应。通过库仑分析获得了[PdI(kappa(2)-2-C6F4PPh2)(PPh(2)Fc)]单电子还原的证据,尽管该产品不稳定并且需要进一步的化学过程。在CH2Cl2中对[Pd-2(mu-Br)(2)(kappa(2)-2-C6F4PPh2)(2)](7)进行制备性电还原会导致其Pd-Cσ键的还原裂解并形成配合物[PdBr2 {PPh2(2-C6F4H)}(2)](14);讨论了可能的机制。

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