Electrochemical method synthesis

Electrochemical Synthesis. Electrochemical methods have also been investigated for the synthesis of polysilanes, but these have so far yielded low molecular weight materials (113,114). 

Soluble and weU-characterized polygermane homopolymers, (R Ge), and their copolymers with polysdanes have been prepared by the alkaH metal coupling of diorgano-substituted dihalogermanes (137—139), via electrochemical methods (140), and by transition-metal catalyzed routes (105), as with the synthesis of polysdanes. 

The procedure described is essentially that of Belleau and Weinberg and represents the only known way of obtaining the title compound. One other quinone acetal, 1,4,9,12-t6traoxadispiro[4.2.4.2]tetradeea-6,13-diene, has been synthesized by a conventional method (reaction of 1,4-cyclohexanedione with ethylene glycol followed by bromination and dehydrobromination ) as well as by an electrochemical method (anodic oxidation of 2,2-(l,4-phenylenedioxy)diethanol ). Quinone acetals have been used as intermediates in the synthesis of 4,4-dimethoxy-2,5-cyclohexadienone,. syw-bishomoquinone, - and compounds related to natural products. ... 

Electrochemical methods may also be used in the synthesis of chalcogen-nitrogen compounds. For example, the electrochemical reduction of salts of the [SsNs]" cation (Section 5.3.9) in SO2 or CH2CI2 at low temperatures produces microcrystals of the superconducting polymer (SN). ... 

Preparation of Memfield resin-bound nitro acetates, which is a suitable bndding block for the development of combinatorial solid phase synthesis, is repotted. The anion of ethyl nitro acetate is generated in DMF by an electrochemical method using Pt cathode, magnesium rod anode, and tetrabutylairunonium bromide as an electrolyte. Alkylaton of this anion with alkyl hahdes gives mono-alkylated products in 80% yield." ... 

Electroorganic Synthesis by Indirect Electrochemical Methods New Applications of Electrochemical Techniques ... 

Noteworthy, irradiation and electrochemical methods have important advantages for the synthesis of metal NPs in ILs. Since they do not generate by-products, these methods are considered the cleanest procedures for obtaining stable metal NPs. Selected examples are summarized in Table 1.1. 

The electrosynthesis of metalloporphyrins which contain a metal-carbon a-bond is reviewed in this paper. The electron transfer mechanisms of a-bonded rhodium, cobalt, germanium, and silicon porphyrin complexes were also determined on the basis of voltammetric measurements and controlled-potential electrooxidation/reduction. The four described electrochemical systems demonstrate the versatility and selectivity of electrochemical methods for the synthesis and characterization of metal-carbon o-bonded metalloporphyrins. The reactions between rhodium and cobalt metalloporphyrins and the commonly used CH2CI2 is also discussed. 

In summary, the four chemical systems described in this paper demonstrate the versatility and selectivity of electrochemical methods for synthesis and characterization of metal-carbon a-bonded metalloporphyrins. The described rhodium and cobalt systems demonstrate significant differences with respect to their formation, stability and to some extend, reactivity of the low valent species. On the other hand, properties of the electroche-mically generated mono-alkyl or mono-aryl germanium and silicon systems are similar to each other. 

Polyfluorobenzyl alcohols are one class of fluorinated starting materials for medicinal and agricultural usage. Practical electrochemical methods for the product-selective synthesis of polyfluorobenzyl alcohols have been developed [79, 80], 2,3,4,5,6-Pentafluorobenzoic acid is reduced selectively to 2,3,4,5,6-pentafluorobenzyl alcohol at amalgamated lead, zinc and cadmium cathodes in aqueous sulfuric acid solutions, while 2,3,5,6-tetrafluorobenzyl alcohol can also be obtained selectively by using the non-amalgamated cathodes in solutions containing small amounts of a quartemary ammonium salt [79],... 

Recently, acylsilanes have been utilized as useful intermediates in organic synthesis [57], For example, treatment of acylsilanes with the fluoride ion generates the corresponding acyl anions which react with electrophiles. On the other hand, by using the electrochemical method, acylsilanes serve as acyl cation equivalents because nucleophiles are introduced at the carbonyl carbon. Chemical oxidation of acylsilanes with hydrogen peroxide which affords the corresponding carboxylic acids has been reported [58], However, the anodic oxidation provides a versatile method for the introduction of various nucleophiles... 

Utley JHP, Electrochemical methods for organic synthesis Fundamentals and applications, in ref (45)... 

Reetz, M.T., Helbig W., and Quaiser, S.A., Electrochemical methods in the synthesis of nanostructured transition metal clusters, in Active Metals, Ftirstner, A., Ed., VCH, Weinheim, 1996, p. 279. 

We chose to study the generation of alkoxycarbenium ion 26 from thioacetal 28. The electrochemically generated ArS(ArSSAr)+, 37 which was well characterized by CSI-MS, was found to be quite effective for the generation of alkoxycarbenium ions, presumably because of its high thiophilicity (Scheme 17). The conversion of 28 to 26 requires 5 min at -78 °C. The alkoxycarbenium ion pool 26 thus obtained exhibited similar stability and reactivity to that obtained with the direct electrochemical method. The indirect cation pool method serves a powerful tool not only for mechanistic studies on highly reactive cations but also for rapid parallel synthesis. 

Comparison of Chemical and Electrochemical Methods in Organic Synthesis... 

In addition, the idea of the terpenoid side chain of 10 essentially assisting in anchoring the coenzyme in the cytoplasmic membrane without having any impact on the redox potential was to be explored. To this end, a number of phenazine ethers 44a-g were synthesized by Williamson ether synthesis and then investigated by electrochemical methods. And indeed, we were able to identify a good match between the redox potentials of the various phenazine ethers, which turned out to be independent of the side chain structure. 

Yamamura S (1995) Synthetic studies on natural products using electrochemical method as a key step. In Torii, S (ed) Novel trends in electroorganic synthesis, Kodansha, Tokyo, pg265... 

---