Literature DB >> 25865439

Facile hydrolysis and alcoholysis of palladium acetate.

Robin B Bedford1, John G Bowen2, Russell B Davidson2, Mairi F Haddow2, Annabelle E Seymour-Julen2, Hazel A Sparkes2, Ruth L Webster2,3.   

Abstract

Palladium(II) acetate is readily converted into [Pd3 (μ(2) -OH)(OAc)5 ] (1) in the presence of water in a range of organic solvents and is also slowly converted in the solid state. Complex 1 can also be formed in nominally anhydrous solvents. Similarly, the analogous alkoxide complexes [Pd3 (μ(2) -OR)(OAc)5 ] (3) are easily formed in solutions of palladium(II) acetate containing a range of alcohols. An examination of a representative Wacker-type oxidation shows that the Pd-OH complex 1 and a related Pd-oxo complex 4 can be excluded as potential catalytic intermediates in the absence of exogenous water.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  acetate ligands; homogeneous catalysis; hydrolysis; oxidation; palladium

Year:  2015        PMID: 25865439     DOI: 10.1002/anie.201500620

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Ligand-accelerated non-directed C-H functionalization of arenes.

Authors:  Peng Wang; Pritha Verma; Guoqin Xia; Jun Shi; Jennifer X Qiao; Shiwei Tao; Peter T W Cheng; Michael A Poss; Marcus E Farmer; Kap-Sun Yeung; Jin-Quan Yu
Journal:  Nature       Date:  2017-11-22       Impact factor: 49.962

2.  Palladium(II)-Catalysed Aminocarbonylation of Terminal Alkynes for the Synthesis of 2-Ynamides: Addressing the Challenges of Solvents and Gas Mixtures.

Authors:  N Louise Hughes; Clare L Brown; Andrew A Irwin; Qun Cao; Mark J Muldoon
Journal:  ChemSusChem       Date:  2017-01-23       Impact factor: 8.928

  2 in total

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