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Copper function

The main by-products of the Ullmaim condensation are l-aniinoanthraquinone-2-sulfonic acid and l-amino-4-hydroxyanthraquinone-2-sulfonic acid. The choice of copper catalyst affects the selectivity of these by-products. Generally, metal copper powder or copper(I) salt catalyst has a greater reactivity than copper(Il) salts. However, they are likely to yield the reduced product (l-aniinoanthraquinone-2-sulfonic acid). The reaction mechanism has not been estabUshed. It is very difficult to clarify which oxidation state of copper functions as catalyst, since this reaction involves fast redox equiUbria where anthraquinone derivatives and copper compounds are concerned. Some evidence indicates that the catalyst is probably a copper(I) compound (28,29). [Pg.310]

Fig. 18. Catalytic cycle of the amine oxidases. Only TOPA quinone is required for catalysis copper functions solely as a cofactor in its synthesis. From [28] with permission... Fig. 18. Catalytic cycle of the amine oxidases. Only TOPA quinone is required for catalysis copper functions solely as a cofactor in its synthesis. From [28] with permission...
Purification of metals is another important application of electrolysis. For example, impure copper from the chemical reduction of copper ore is cast into large slabs that serve as the anodes for electrolytic cells. Aqueous copper sulfate is the electrolyte, and thin sheets of ultrapure copper function as the cathodes (see Fig. 18.23). [Pg.855]

To verify the modelling of the data eolleetion process, calculations of SAT 4, in the entrance window of the XRII was compared to measurements of RNR p oj in stored data as function of tube potential. The images object was a steel cylinder 5-mm) with a glass rod 1-mm) as defect. X-ray spectra were filtered with 0.6-mm copper. Tube current and exposure time were varied so that the signal beside the object. So, was kept constant for all tube potentials. Figure 8 shows measured and simulated SNR oproj, where both point out 100 kV as the tube potential that gives a maximum. Due to overestimation of the noise in calculations the maximum in the simulated values are normalised to the maximum in the measured values. Once the model was verified it was used to calculate optimal choice of filter materials and tube potentials, see figure 9. [Pg.212]

Figure 2.2. Second-order rate constant for the Diels-Alder reaction of 2.4a with 2.5 in aqueous solution as a function of the concentrations of copper(II)ni trate. Figure 2.2. Second-order rate constant for the Diels-Alder reaction of 2.4a with 2.5 in aqueous solution as a function of the concentrations of copper(II)ni trate.
Unfortunately, addition of copper(II)nitrate to a solution of 4.42 in water did not result in the formation of a significant amount of complex, judging from the unchanged UV-vis absorption spectrum. Also after addition of Yb(OTf)3 or Eu(N03)3 no indications for coordination were observed. Apparently, formation of a six-membered chelate ring containing an amine and a ketone functionality is not feasible for these metal ions. Note that 4.13 features a similar arrangement and in aqueous solutions, likewise, does not coordinate significantly to all the Lewis acids that have been... [Pg.114]

A characteristic property of an aldehyde function is its sensitivity to oxidation A solu tion of copper(II) sulfate as its citrate complex (Benedict s reagent) is capable of oxi dizing aliphatic aldehydes to the corresponding carboxylic acid... [Pg.1053]

Oxidation with Benedict s reagent (Section 25 19) Sugars that con tain a free hemiacetal function are called reducing sugars They react with copper(ll) sulfate in a sodium citrate/sodium carbonate buffer (Benedict s reagent) to form a red precipitate of copper(l) oxide Used as a qualitative test for reducing sugars... [Pg.1063]

The reactors were thick-waked stainless steel towers packed with a catalyst containing copper and bismuth oxides on a skiceous carrier. This was activated by formaldehyde and acetylene to give the copper acetyUde complex that functioned as the tme catalyst. Acetylene and an aqueous solution of formaldehyde were passed together through one or more reactors at about 90—100°C and an acetylene partial pressure of about 500—600 kPa (5—6 atm) with recycling as required. Yields of butynediol were over 90%, in addition to 4—5% propargyl alcohol. [Pg.106]

Fluorine can be handled using a variety of materials (100—103). Table 4 shows the corrosion rates of some of these as a function of temperature. System cleanliness and passivation ate critical to success. Materials such as nickel, Monel, aluminum, magnesium, copper, brass, stainless steel, and carbon steel ate commonly used. Mote information is available in the Hterature (20,104). [Pg.129]

Aerosol-Based Direct Fluorination. A technology that works on Hter and half-Hter quantities has been introduced (40—42). This new aerosol technique, which functions on principles similar to LaMar direct fluorination (Fig. 5), uses fine aerosol particle surfaces rather than copper filings to maintain a high surface area for direct fluorination. The aerosol direct fluorination technique has been shown to be effective for the synthesis of bicycHc perfluorocarbon such as perfluoroadamantane, perfluoroketones, perfluoroethers, and highly branched perfluorocarbons. [Pg.278]

A further improvement in the cuprate-based methodology for producing PGs utilizes a one-pot procedure (203). The CO-chain precursor (67) was first functionalized with zirconocene chloride hydride ia THF. The vinyl zirconium iatermediate was transmetalated direcdy by treatment with two equivalents of / -butyUithium or methyUithium at —30 to —70° C. Sequential addition of copper cyanide and methyUithium eUcited the /V situ generation of the higher order cyanocuprate which was then reacted with the protected enone to give the PG. [Pg.162]

For slightly less than 10% of products, alloying elements are introduced to produce properties not available for carbon steels where the functional elements are usually considered to be carbon, siHcon (to 0.6%), and manganese (to 1.65%). Copper, which may be present up to 0.6 wt %, is relatively rare compared to the ubiquitous siHcon and manganese. [Pg.396]


See other pages where Copper function is mentioned: [Pg.962]    [Pg.497]    [Pg.2565]    [Pg.961]    [Pg.313]    [Pg.446]    [Pg.508]    [Pg.688]    [Pg.87]    [Pg.962]    [Pg.497]    [Pg.2565]    [Pg.961]    [Pg.313]    [Pg.446]    [Pg.508]    [Pg.688]    [Pg.87]    [Pg.214]    [Pg.2224]    [Pg.113]    [Pg.321]    [Pg.208]    [Pg.252]    [Pg.280]    [Pg.125]    [Pg.150]    [Pg.374]    [Pg.384]    [Pg.31]    [Pg.241]    [Pg.549]    [Pg.132]    [Pg.202]    [Pg.385]    [Pg.422]    [Pg.229]    [Pg.560]    [Pg.72]    [Pg.363]    [Pg.443]    [Pg.174]    [Pg.403]    [Pg.61]    [Pg.285]   
See also in sourсe #XX -- [ Pg.338 , Pg.339 ]

See also in sourсe #XX -- [ Pg.369 ]

See also in sourсe #XX -- [ Pg.727 ]

See also in sourсe #XX -- [ Pg.439 , Pg.440 ]




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