Reduction metal halides

Mechanism of Meta Hydride-Transition Metal Halide Reductions... 

The utility of metal hydride-transition metal halide reductions is limited only to alkenes and alkynes which do not contain functional groups which can react with the metal hydride, or with potential low-valent transition metal species. This severely limits the use of this reaction. 

Where the nature of the metal or experimental conditions render such auxiliary complexation with either the substrate or the solvent less favorable, there is an increased tendency towards homolysis of the carbon-metal bond. Treatment of organolithium and organomagnesium alkyls with transition metal halides leads to metal halide reduction and hydrocarbon, suggestive of the transitory formation of metal alkyls (45), decomposing thereupon into a lower salt and free alkyl radicals ... 

Gold and Silver films have been prepared by pyrolysis and metal halide reduction [100,191]. 

The 17-ethylene ketal of androsta-l,4-diene-3,17-dione is reduced to the 17-ethylene ketal of androst-4-en-3,17-dione in about 75% yield (66% if the product is recrystallized) under the conditions of Procedure 8a (section V). However, metal-ammonia reduction probably is no longer the method of choice for converting 1,4-dien-3-ones to 4-en-3-ones or for preparing 5-en-3-ones (from 4,6-dien-3-ones). The reduction of 1,4-dien-3-ones to 4-en-3-ones appears to be effected most conveniently by hydrogenation in the presence of triphenylphosphine rhodium halide catalysts. Steroidal 5-en-3-ones are best prepared by base catalyzed deconjugation of 4-en-3-ones. ... 

As in the previous group, a potentially productive route into C7-ring chemistry is provided by the reduction of a metal halide with Na/Hg in thf in the presence of cycloheptatriene. WithMoCl5, [Mo(p -C7H7)(p -C7H9)] is produced and a variety of derivatives have already been obtained. 

In the second part of the 20th century, the tantalum capacitor industry became a major consumer of tantalum powder. Electrochemically produced tantalum powder, which is characterized by an inconsistent dendrite structure, does not meet the requirements of the tantalum capacitor industry and thus has never been used for this purpose. This is the reason that current production of tantalum powder is performed by sodium reduction of potassium fluorotantalate from molten systems that also contain alkali metal halides. The development of electronics that require smaller sizes and higher capacitances drove the tantalum powder industry to the production of purer and finer powder providing a higher specific charge — CV per gram. This trend initiated the vigorous and rapid development of a sodium reduction process. 

Transition metal complexes that are easy to handle and store are usually used for the reaction. The catalytically active species such as Pd(0) and Ni(0) can be generated in situ to enter the reaction cycle. The oxidative addition of aryl-alkenyl halides can occur to these species to generate Pd(II) or Ni(II) complexes. The relative reactivity for aryl-alkenyl halides is RI > ROTf > RBr > RC1 (R = aryl-alkenyl group). Electron-deficient substrates undergo oxidative addition more readily than those electron-rich ones because this step involves the oxidation of the metal and reduction of the organic aryl-alkenyl halides. Usually... 

Hydrogen reduction has a major advantage in that the reaction generally takes place at lower temperature than the equivalent decomposition reaction. It is used extensively in the deposition of transition metals from their halides, particularly the metals of Groups Va, (vanadium, niobium, and tantalum) and Via (chromium, molybdenum, and tungsten). The halide reduction of Group IVa metals (titanium, zirconium, and hafnium) is more difficult because their halides are more stable. 

The hydrogen reduction of the metal halides, described in Sec. 1.2, is generally the favored reaction for metal deposition but is not suitable for the platinum-group metals since the volatilization and decomposition temperatures of their halides are too close to provide efficient vapor transport. 1 1 For that reason, the decomposition of the carbonyl halide is preferred. The exception is palladium which is much more readily deposited by hydrogen reduction than by the carbonyl-halide decomposition. 

Borides of Group IVa. UB2, ZrB2, and HfB2 are readily deposited by the hydrogen reduction of the metal halide, usually the chloride. Atypical reaction is as follows ... 

Divinylborane-transition-metal complexes ( 6.5.3.1) are accessible from metal halides and divinylboranes with simultaneous reduction by (t -Cp)2Co, e.g. ... 

The platinum metals are valuable by-products from the extraction of common metals such as copper and nickel. The anodic residue that results from copper refining is a particularly important source. The chemistry involved in their purification is too complicated to describe here, except to note that the final reduction step involves reaction of molecular hydrogen with metal halide complexes. 

The possible mechanisms which one might invoke for the activation of these transition metal slurries include (1) creation of extremely reactive dispersions, (2) improved mass transport between solution and surface, (3) generation of surface hot-spots due to cavitational micro-jets, and (4) direct trapping with CO of reactive metallic species formed during the reduction of the metal halide. The first three mechanisms can be eliminated, since complete reduction of transition metal halides by Na with ultrasonic irradiation under Ar, followed by exposure to CO in the absence or presence of ultrasound, yielded no metal carbonyl. In the case of the reduction of WClfc, sonication under CO showed the initial formation of tungsten carbonyl halides, followed by conversion of W(C0) , and finally its further reduction to W2(CO)io Thus, the reduction process appears to be sequential reactive species formed upon partial reduction are trapped by CO. 

The reduction of transition metal halides with Li has been recently extended by Boudjouk and coworkers for Ullman coupling (benzyl halide to bibenzyl) by Cu or Ni, using a low intensity cleaning bath (5J.). Ultrasound dramatically decreased the time required for complete reduction of the metal halides ( 12 h without, <40 minutes with ultrasound). The subsequent reactivity of the Cu or Ni powders was also substantially enhanced by ultrasonic irradiation. This allowed significant increases in the yield of bibenzyl (especially for Ni) at lower temperatures, compared to simple stirring. 

Similarly, Kou et al. published the synthesis of PVP-stabilized noble-metal nanoparticles in ionic liquids BMI PF6 at room temperature [76]. The metal nanoparticles (Pt, Pd, Rh) were produced by reduction of the corresponding metal halide salts in the presence of PVP into a refluxing ethanol-water solution. After evaporation to dryness the residue was redissolved in methanol and the solution added to the ionic liquid. The methanol was then removed by evaporation to give the ionic liquid-immobilized nanoparticles. These nanoparticles were very stable. TEM ob-... 

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