Oxidative aromatization of olefins with dioxygen catalyzed by palladium trifluoroacetate

Molecular oxygen can replace sacrificial olefins as the hydrogen acceptor in the palladium trifluoroacetate catalyzed dehydrogenation of cyclohexene and related cyclic olefins into aromatics. One of the major drawbacks of the homogeneous system is the tendency of the palladium trifluoroacetate to precipitate as palladium(0) at elevated temperatures. The use of better ligands affords catalysts that can operate at higher temperatures, although they are less reactive than palladium trifluoroacetate

Glycerol as a cheap, safe and sustainable solvent for the catalytic and regioselective β,β-diarylation of acrylates over palladium nanoparticles

Herein we show that glycerol can be considered as a promising cheap and green solvent for the regioselective β,β-diarylation of alkenes. Whereas this reaction is generally catalyzed under an inert atmosphere by expensive phosphine or carbene-palladium complexes, we show here that the diarylation of alkenes can be conveniently achieved in glycerol in the presence of air-stable palladium nanoparticles. These palladium nanoparticles were stabilized over a sugar-based surfactant derived from biomass. By an adjustment of the reaction temperature, we were able to control the mono- and diarylation step of alkenes, thus offering a convenient route to unsymmetrical diarylated alkenes. At the end of the reaction, the diarylated alkenes were cleanly and selectively extracted from the glycerol-palladium catalytic phase using supercritical carbon dioxide, thus affording a convenient purification work-up. Within the framework of green chemistry, this work combines (i) catalysis in a cheap, safe and sustainable medium, (ii) easily made and air-stable palladium nanoparticles as the catalyst, and (iii) a clean and selective extraction of the reaction products with supercritical carbon dioxide

Laser-induced prenucleation of alumina for electroless plating

This paper deals with the deposition of palladium from decomposition of a thin palladium acetate layer on rough and porous alumina ceramic surfaces by irradiating it with a UV excimer laser. The palladium acetate layer was formed from a combination of propyl glycol methyl ether acetate solvent and photoresist, and the undecomposed material was removed with the photoresist remover. The discontinuous palladium cluster film formed by the technique was used as seed for electroless coatings. Different patterns were obtained using point focus as well as projection pattering method and subsequently plated with adhesive layers of electroless Ni-B coating

Inflating hollow nanocrystals through a repeated Kirkendall cavitation process.

The Kirkendall effect has been recently used to produce hollow nanostructures by taking advantage of the different diffusion rates of species involved in the chemical transformations of nanoscale objects. Here we demonstrate a nanoscale Kirkendall cavitation process that can transform solid palladium nanocrystals into hollow palladium nanocrystals through insertion and extraction of phosphorus. The key to success in producing monometallic hollow nanocrystals is the effective extraction of phosphorus through an oxidation reaction, which promotes the outward diffusion of phosphorus from the compound nanocrystals of palladium phosphide and consequently the inward diffusion of vacancies and their coalescence into larger voids. We further demonstrate that this Kirkendall cavitation process can be repeated a number of times to gradually inflate the hollow metal nanocrystals, producing nanoshells of increased diameters and decreased thicknesses. The resulting thin palladium nanoshells exhibit enhanced catalytic activity and high durability toward formic acid oxidation

Confirming the existence of π-allyl-palladium intermediates during the reaction of meta photocycloadducts with palladium(ii) compounds

The transient existence of π-allyl-palladium intermediates formed by the reaction of Pd(OAc)2 and anisole-derived meta photocycloadducts has been demonstrated using NMR techniques. The intermediates tended to be short-lived and underwent rapid reductive elimination of palladium metal to form allylic acetates, however this degradation process could be delayed by changing the reaction solvent from acetonitrile to chloroform

Dichloropalladium complexes ligated by 4,5-bis(arylimino)pyrenylidenes: Synthesis, characterization, and catalytic behavior towards Heck-reaction

A series of 4,5-bis(arylimino)pyrenylidenylpalladium(II) chloride complexes (C1–C4) were synthesized and characterized by FT-IR and NMR spectroscopy, elemental analysis as well as by single crystal X-ray diffraction for the representative complexes C1 and C3, which revealed a square planar geometry at the palladium center. All palladium complexes exhibited high activity for the Heck cross-coupling reaction, which were effective when conducted in various solvents. Furthermore, the in-situ mixture of palladium dichloride and the ligand (L1) provided an effective catalytic system for the Heck-reaction

Prevention of pressure build-up in electrochemical cells Patent

Preventing pressure buildup in electrochemical cells by reacting palladium oxide with evolved hydroge

ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors.

A new catalyst that derives from commercially available precursors for copper-free, Pd-catalyzed Sonogashira reactions at the sustainable ppm level of precious metal palladium under mild aqueous micellar conditions has been developed. Both the palladium pre-catalyst and ligand are commercially available, bench stable, and highly cost-effective. The catalyst is applicable to both aryl- and heteroaryl-bromides as educts. A wide range of functional groups are tolerated and the aqueous reaction medium can be recycled. An application to a key intermediate associated with an active pharmaceutical ingredient (ponatinib) is discussed