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Copper-based catalyst systems

Our new approach has proven its initial value in both palladium-(Schareina et al. 2004) and copper-catalyzed cyanations (Schareina et al. 2005) and has been adopted by other groups. Very recently, in a joint collaboration with Saltigo GmbH we developed a new and improved copper-based catalyst system, which allows for efficient cyanations of a variety of aromatic and heteroaromatic halides. Importantly, notoriously difficult substrates react in excellent yield and selectivity, making the method applicable on an industrial scale. [Pg.114]

In certain cases, when the palladium or nickel catalyzed coupling is not efficient or fails completely, an alternate solution is provided by the use of copper based catalyst systems. The 5-iodouracil derivative shown in 7.77. was unreactive towards imidazole using either the Buchwald-Hartwig conditions or the copper(I) triflate promoted the carbon-nitrogen bond formation reported by Buchwald98 These latter conditions, however, were effective in coupling the iodouracil with a series of other amines (7.77.), The optimal catalyst system consisted of copper(I) triflate, phenantroline and dibenzylideneacetone (dba).99... [Pg.167]

The aldol (23) on treatment with benzenesulphonyl chloride yields the oxetanone ((3-lactone) (24) which is an intermediate in the synthesis of the butenolides (25) (95SC479). Aliphatic terminal alkynes or arylalkynes react with nitrones in the presence of a copper based catalyst system to give 1,3,4-trisubstituted [3-lactones (95JOC4999). [Pg.70]

A low-pressure process has been developed by ICl operating at about 50 atm (700 psi) using a new active copper-based catalyst at 240°C. The synthesis reaction occurs over a bed of heterogeneous catalyst arranged in either sequential adiabatic beds or placed within heat transfer tubes. The reaction is limited by equilibrium, and methanol concentration at the converter s exit rarely exceeds 7%. The converter effluent is cooled to 40°C to condense product methanol, and the unreacted gases are recycled. Crude methanol from the separator contains water and low levels of by-products, which are removed using a two-column distillation system. Figure 5-5 shows the ICl methanol synthesis process. [Pg.151]

Poly(2,6-dimethyl-l,4-oxyphenylene) (poly(phenylene oxide), PPG) is a material widely used as high-performance engineering plastics, thanks to its excellent chemical and physical properties, e.g., a high 7 (ca. 210°C) and mechanically tough property. PPO was first prepared from 2,6-dimethylphenol monomer using a copper/amine catalyst system. 2,6-Dimethylphenol was also polymerized via HRP catalysis to give a polymer exclusively consisting of 1,4-oxyphenylene unit, while small amounts of Mannich-base and 3,5,3, 5 -tetramethyl-4,4 -diphenoquinone units are always contained in the chemically prepared PPO. [Pg.233]

The replacement of vanadia-based catalysts in the reduction of NOx with ammonia is of interest due to the toxicity of vanadium. Tentative investigations on the use of noble metals in the NO + NH3 reaction have been nicely reviewed by Bosch and Janssen [85], More recently, Seker et al. [86] did not completely succeed on Pt/Al203 with a significant formation of N20 according to the temperature and the water composition. Moreover, 25 ppm S02 has a detrimental effect on the selectivity with selectivity towards the oxidation of NH3 into NO enhanced above 300°C. Supported copper-based catalysts have shown to exhibit excellent activity for NOx abatement. Recently Suarez et al and Blanco et al. [87,88] reported high performances of Cu0/Ni0-Al203 monolithic catalysts with NO/NOz = 1 at low temperature. Different oxidic copper species have been previously identified in those catalytic systems with Cu2+, copper aluminate and CuO species [89], Subsequent additions of Ni2+ in octahedral sites of subsurface layers induce a redistribution of Cu2+ with a surface copper enrichment. Such redistribution... [Pg.308]

Typical catalysts for SCR include supported vanadia, and iron or copper supported on zeolite. Here the application of a model to the design and understanding of vanadia catalyst systems is presented. Over the vanadia-based catalyst system, a Rideal-Eley approach has been adopted by most workers in the field, in which the first step is ammonia adsorption on the catalyst. This stored ammonia can then either react with NOx or be desorbed. Some important contributions to the SCR modelling literature are Andersson et al. (1994), Lietti and Forzatti (1994), Dumesic et al. (1996), Lietti et al. [Pg.84]

The intramolecular reaction between diazo ketones and benzenes is an effective way to generate a range of bicyclic systems.7 The earlier copper-based catalysts have largely been superseded by rho-dium(ll) salts. Unlike the case in the intermolecular reactions, rhodium(ll) acetate is the catalyst that has been most commonly used. Studies by McKervey,133 136 however, indicated that rhodium(II) mandelate, which would be expected to generate a slightly more electrophilic carbenoid than rhodium(ll) acetate, often gave improved yields. [Pg.1055]

Aside from the recently described Cu/Th02 catalysts, copper on chromia and copper on silica have been reported to catalyze methanol synthesis at low temperatures and pressures in various communications that are neither patents nor refereed publications. It is not feasible to critically review statements unsupported by published data or verifiable examples. However, physical and chemical interactions similar to those documented in the copper-zinc oxide catalysts are possible in several copper-metal oxide systems and the active form of copper may be stabilized by oxides of zinc, thorium, chromium, silicon, and many other elements. At the same time it is doubtful that more active and selective binary copper-based catalysts than... [Pg.288]

The improvement in catalyst resistance and the production of impurity-free synthesis gases led to their industrialization. Hence it is now possible to achieve comparable or better performance than that allowed by zinc/chromimn systems, to the extent that the great selectivity of copper-based catalysts reduces the quantity of by-products, by operating between 240 and 270°C. at only 5 to 10.104 Pa absolute, with VHSV ranging from 10,000 to 15,000 h 1 STP (Standard Temperature Pressure) and catalyst lives of over three years. This decisive improvement was achieved on the initiative of iCL... [Pg.89]

A majority of the literature on ATRP focuses on the synthesis of styrene and its derivatives with copper-based catalysts. One of the most extensively studied systems is the polymerization of styrene conducted with CuBr, nitrogen-based ligands, and alkyl bromides as initiator. Better molecular weight control is obtained at low temperatures, presumably due to a lower contribution of thermal self-initiation during the early stage of the polymerization. For example, the reaction temperature can be lowered to 80-90 °C when efficient catalysts, such as CuBr/PMDETA, are used [19-22, 30]. [Pg.28]


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See also in sourсe #XX -- [ Pg.186 ]




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