Activated formic acid

C H23N70s, Mr 445.43, [a] +14.9° (0.1 M NaOH). A coenzyme, unstable in solution and in the air, that transfers a one-carbon unit in metabolic processes (C, activated formaldehyde, activated formic acid ) (see... 

Abstract Direct liquid fuel cells for portable electronic devices are plagued by poor efficiency due to high overpotentials and accumulation of intermediates on the electrocatalyst surface. Direct formic acid fuel cells have a potential to maintain low overpotentials if the electrocatalyst is tailored to promote the direct electrooxidation pathway. Through the understanding of the structural and environmental impacts on preferential selection of the more active formic acid electrooxidation pathway, a higher performing and more stable electrocatalyst is sought. This chapter overviews the formic acid electrooxidation pathways, enhancement mechanisms, and fundamental electrochemical mechanistic studies. 

F ormyltransferases 5,10-Methenyltetra-hydrofolate, 10-formyltetrahy dro-folate ( activated formic acid ) Glycineamide ribonucleotide transformylase (D 10.4) 5-Aminoimidazole-4-carboxamide ribonucleotide transformylase (D 10.4)... 

If you netralize the formic acid mix with 25% NaOH the layers separate out nicely. It takes 75 / of 25% NaOH to neutralize the soln for 150grm 88% formic, so you ll need a big sepatory funnel. After you hit ph 4.5 add it rery carefully cause it ll run away to 9+ real quick. You can then back extract the water with DCM, or I guess preferably ether. If you use too much DCM when extracting it sinks to the bottom and some product floats on the top, so you end up with three layers... But then my lab tech SUXSI (not that I d partake in iilegal activities. p"... 

The uses of dimethyl acetamide are very similar to those for dimethylform amide [68-12-2] (see FoRMiC ACId). DMAC is employed most often where higher temperatures are needed for solution of resins or activation of chemical reactions. 

Ion implantation has also been used for the creation of novel catalyticaHy active materials. Ruthenium oxide is used as an electrode for chlorine production because of its superior corrosion resistance. Platinum was implanted in mthenium oxide and the performance of the catalyst tested with respect to the oxidation of formic acid and methanol (fuel ceU reactions) (131). The implantation of platinum produced of which a catalyticaHy active electrode, the performance of which is superior to both pure and smooth platinum. It also has good long-term stabiHty. The most interesting finding, however, is the complete inactivity of the electrode for the methanol oxidation. 

Activators. Activators are often added to removers to make them more efficient. Acids such as phenol [108-95-2] phosphoric acid [7664-38-2] acetic acid [64-19-7] formic acid [64-18-6]., and citric acid [5949-29-1] are used to increase the cutting abiHty on epoxide-type paints and other modem finishes. Strongly alkaline activators are effective on enamel andlatex paints. Other activators include ammonia [7664-41-7] monoethyl amine [75-04-7], and /V-phenyIdiethan ol amines. Acid and base activators shorten the shelf life of some removers. 

The rate of stripping or the stripabiUty on cataly2ed urethane and epoxy resin finishes can be increased by adding formic acid, acetic acid, and phenol. Sodium hydroxide, potassium hydroxide, and trisodium phosphate [10101-89-0] may be added to the formula to increase the stripabiUty on enamel and latex paints. Other activators include oleic acid [112-80-17, trichloroacetic acid [76-85-9], ammonia, triethanolamine [102-71-6], and monoethyl amine. Methylene chloride-type removers are unique in their abiUty to accept cosolvents and activators that allow the solution to be neutral, alkaline, or acidic. This abihty gready expands the number of coatings that can be removed with methylene chloride removers. 

In a series of organic acids of similar type, not much tendency exists for one acid to be more reactive than another. For example, in the replacement of stearic acid in methyl stearate by acetic acid, the equilibrium constant is 1.0. However, acidolysis in formic acid is usually much faster than in acetic acid, due to higher acidity and better ionizing properties of the former (115). Branched-chain acids, and some aromatic acids, especially stericaHy hindered acids such as ortho-substituted benzoic acids, would be expected to be less active in replacing other acids. Mixtures of esters are obtained when acidolysis is carried out without forcing the replacement to completion by removing one of the products. The acidolysis equilibrium and mechanism are discussed in detail in Reference 115. 

The anticonvulsant primidone (1035) resembles phenobarbital but lacks the 2-oxo substituent. It was introduced in 1952 and has remained a valuable drug for controlling grand mal and psychomotor epilepsy. As might be expected, primidone is metabolized to yield phenobarbital (1034 X = 0) and C-ethyl-C-phenylmalondiamide (1036), both of which have marked anticonvulsant properties however, primidone does have intrinsic activity and an appropriate mixture of its metabolites has only a fraction of its activity (73MI21303). Primidone may be made in several ways, of which desulfurization by Raney nickel of the 2-thiobarbiturate (1034 X = S) or treatment of the diamide (1036) with formic acid (at 190 °C) seem to be the most satisfactory (54JCS3263). 

Hess and Eichel have shown that d-coniine with formaldehyde and formic acid yields an active A -methyl-d-coniine, and that methylZso-pelletierine hydrazone (see p. 57) yields ZV-methyl-dZ-coniine when heated with sodium ethoxide at 150-70°. 

It appears that chromium(III) is an essential trace element in mammalian metabolism and, together with insulin, is responsible for the clearance of glucose from the blood-stream. Tungsten too has been found to have a role in some enzymes converting CO2 into formic acid but, from the point of view of biological activity, the focus of interest in this group is unquestionably on molybdenum. 

In an interesting analogy to the penicillin series, acylation of 7-ACA with the phenylglycine moiety affords a compound with oral activity. Thus, phenylglycine is first protected as the carbo tertiary butyloxy derivative (45). Reaction of this with isobutyloxy chloroformate affords the mixed anhydride (46). Condensation of that with 7-ACA gives the intermediate, 47. Treatment with either trifluoroacetic or formic acid provides the free amine cephaloglycin (48). ... 

A derivative of an isomeric azapurine ring system interestingly exhibits bronchodilator activity, possibly indicating interaction with a target for theophylline. The starting pyridazine 97 is available from dichloro compound 96 by sequential replacement of the halogens. Treatment of 97 with formic acid supplies the missing carbon and cyclizes the intermediate formamide with consequent formation of zindotrine (98) [16]. 

PCSs obtained by dehydrochlorination of poly(2-dilorovinyl methyl ketones) catalyze the processes of oxidation and dehydrogenation of alcohols, and the toluene oxidation207. The products of the thermal transformation of PAN are also catalysts for the decomposition of nitrous oxide, for the dehydrogenation of alcohols and cyclohexene274, and for the cis-tnms isomerization of olefins275. Catalytic activity in the decomposition reactions of hydrazine, formic acid, and hydrogen peroxide is also manifested by the products of FVC dehydrochlorination... 

As early as 1923 Hinshelwood and Topley (27) noted the exceptionally erratic behavior of palladium foil catalyst in the formic acid decomposition reaction within 140-200°C. The initially very high catalytic activity decreased 102 times during the exposure of palladium to hydrogen, which is a product of the reaction. Though the interpretation does not concern the /3-hydride formation, the authors observation deserves mentioning. 

Fig. 8. Arrhenius plots for the formic acid decomposition on palladium foil (1) and small pieces of this foil (2) at a higher temperature range, when hydrogen evolving as a product of the reaction was absorbed by Pd and transformed into the /3-Pd-H hydride phase. At the lower temperature range the reaction proceeds on the a-Pd-H phase, with a higher activation energy when the foil was hydrogen pretreated (2a), and a lower activation energy for a degassed Pd foil (3a). After Brill and Watson (57).

Volter and Alsdorf (52) obtained a relation of a very similar character for the dependence of the catalytic activity in formic acid decomposition on the composition of the nickel-copper alloys. However, extending the times of the alloy annealing for their better homogenization caused the maxima on the catalytic activity curves to disappear. 

Polypyrrole shows catalytic activity for the oxidation of ascorbic acid,221,222 catechols,221 and the quinone-hydroquinone couple 223 Polyaniline is active for the quinone-hydroquinone and Fe3+/Fe2+ couples,224,225 oxidation of hydrazine226 and formic acid,227 and reduction of nitric acid228 Poly(p-phenylene) is active for the oxidation of reduced nicotinamide adenine dinucleotide (NADH), catechol, ascorbic acid, acetaminophen, and p-aminophenol.229 Poly(3-methylthiophene) catalyzes the electrochemistry of a large number of neurotransmitters.230... 

The oxidation of formic acid by Ce(IV) sulphate which is reported as being very slow, is accelerated by X-irradiation OH- is the active oxidant. 

Cathodic reduction is the most promising approach to the removal of carbon dioxide from a closed atmosphere. Methods developed so far provide for electrode materials, electrolytes, and electrolysis conditions where CO2 can be reduced to hquid organic products of low molecular weight such as formic acid. More complex systems are required to regenerate foodstuffs from the rejects of human vital activities during... 

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