Subject radical chain

This is an extremely important reaction to which we wiU refer throughout this book. It is responsible for all NO, formation in the atmosphere (the brown color of the air over large cities) as well as nitric acid and acid rain. This reaction only occurs in high-temperature combustion processes and in lightning bolts, and it occurs in automobile engines by free-radical chain reaction steps, which will be the subject of Chapter 10. It is removed from the automobile exhaust in the automotive catalytic converter, which wiU be considered in Chapter 7. 

The alkylation of quinoline by decanoyl peroxide in acetic acid has been studied kineti-cally, and a radical chain mechanism has been proposed (Scheme 207) (72T2415). Decomposition of decanoyl peroxide yields a nonyl radical (and carbon dioxide) that attacks the quinolinium ion. Quinolinium is activated (compared with quinoline) towards attack by the nonyl radical, which has nucleophilic character. Conversely, the protonated centre has an unfavorable effect upon the propagation step, but this might be reduced by the equilibrium shown in equation (167). A kinetic study revealed that the reaction is subject to crosstermination (equation 168). The increase in the rate of decomposition of benzoyl peroxide in the phenylation of the quinolinium ion compared with quinoline is much less than for alkylation. This observation is consistent with the phenyl having less nucleophilic character than the nonyl radical, and so it is less selective. Rearomatization of the cr-complex formed by radicals generated from sources other than peroxides may take place by oxidation by metals, disproportionation, induced decomposition or hydrogen abstraction by radical intermediates. When oxidation is difficult, dimerization can take place (equation 169). 

Kharasch and Mayo in 1933," in the first of many papers on the subject, showed that the addition of HBr to allyl bromide in the presence of light and air occurs rapidly to yield 1,3-dibromopropane, whereas in the absence of air and with purified reagents, the reaction is slow and 1,2-dibromopropane is formed. The latter reaction is the normal addition occurring by an ionic pathway giving the Markovnikov orientation. In 1933 the mechanism of the abnormal process ( anti-Markovnikov addition) was not discussed, and it was only in 1937 that the free radical chain mechanism for this process was proposed by Kharasch and his co-workers. "" The mechanism was extended to propene, for which the role of peroxides in promoting the reaction was demonstrated (equations 30, 31). This mechanism was also proposed... 

Halpern et al. had already stressed the importance of radical mechanisms in the oxidative addition and insertion reactions of both [Rh(OEP)]2 and Rh(OEP) [338]. Thus, [Rh(OEP)]2 reacted with trimethylphosphite according to sequence (37), forming a rhodiophosphonate Rh(PO OMe 2) (OEP) and methyl radicals which were subject to further reactions [339]. In the presence of excess P(OMe)3, they were trapped by formation of MePO(OMe)2 in more than stoichiometric quantities, indicating a radical chain process. 

Unsaturated fatty acids in foods are very susceptible to oxidation by oxygen in the air during processing and storage. The oxidation results initially in the formation of fatty acid hydroperoxides by a free radical chain mechanism. The hydroperoxides are subject to several further reactions forming secondary products such as aldehydes, ketones, and other volatile compounds, many of which are odorous and cause rancid flavor in the food. This development of rancid flavor limits the storage stability of a large number of food products. 

Pyrolysis of acetylene to a mixture of aromatic hydrocarbons has been the subject of many studies, commencing with the work of Berthelot in 1866 (1866a, 1866b). The proposed mechanisms have ranged from formation of CH fragments by fission of acetylene (Bone and Coward, 1908) to free-radical chain reactions initiated by excitation of acetylene to its lowest-lying triplet state (Palmer and Dormisch, 1964 Palmer et al., 1966) and polymerization of monomeric or dimeric acetylene biradicals (Minkoff, 1959 see also Cullis et al., 1962). Photosensitized polymerization of acetylene and acetylene-d2 and isotopic analysis of the benzene produced indicated involvement of both free-radical and excited state mechanisms (Tsukuda and Shida, 1966). 

Allyl)Fp complexes are also subject to attack, at C-3, by radicals. The mechanism of allylic transposition of ()] -allyl)Fp complexes, as well as the mechanism of phosphite substitution for CO, has been ascribed to attack by Cp(CO)(L)Fe- on the original Fp-aUyl. The reaction of (12) with CCI4 proceeds by a radical chain mechanism, ultimately between CCI3 and the Fp-allyl. The substitution of a-halo ketones and esters most likely proceeds similarly. A radical cation coupling mechanism has been proposed for the dimerization of (jj -allyl)Fp and (j7 -propargyl)Fp complexes. ... 

Neat A-(l -methyl-4-pentenyl)hydroxylamine underwent facile cyclization to the corresponding Y-hydroxypyrrolidine 1 on wanning briefly to 50- 60 °C, via a radical chain reaction involving the nitroxide radical. A-(l-Methyl-5-hexenyl)hydroxylamine cyclized to give A-hydroxypipe-ridine 2 only in refluxing xylene under high dilution conditions, this is necessary to avoid formation of byproducts. The cyclization was facilitated by the presence of a-methyl substituents in the hydroxylamine. Transannular cyclization of A-[(3-cyclohexenyl)methyl]hydroxylamine was not successful. Since the isolation of pure samples of the water-soluble and easily oxidized hydroxylamines was not a satisfactory procedure, the crude reaction mixtures were subjected to reduction with a zinc/acetic acid/acetic anhydride system to isolate acetylated cyclic amines. 

Both intermolecular and intramolecular additions of carbon radicals to alkenes and alkynes continue to be a widely investigated method for carbon-carbon bond formation and has been the subject of a number of review articles. In particular, the inter- and intra-molecular additions of vinyl, heteroatomic and metal-centred radicals to alkynes have been reported and also the factors which influence the addition reactions of carbon radicals to unsaturated carbon-carbon bonds. The stereochemical outcome of such additions continues to attract interest. The generation and use of alkoxy radicals in both asymmetric cyclizations and skeletal rearrangements has been reviewed and the use of fi ee radical reactions in the stereoselective synthesis of a-amino acid derivatives has appeared in two reports." The stereochemical features and synthetic potential of the [1,2]-Wittig rearrangement has also been reviewed. In addition, a review of some recent applications of free radical chain reactions in organic and polymer synthesis has appeared. The effect of solvent upon the reactions of neutral fi ee radicals has also recently been reviewed. ... 

Decarboxylation of acids by photolysis of their N-hydroxy-pyridine-2-thione esters has been the subject of much study. The reaction proceeds by way of a radical chain pathway and involves... 

When the pyrolytic process does not occur in gas phase, different problems appear. Although equations of the type (6) with k expressed by rel. (5) or (14) can be used in certain cases, these may lead to incorrect results in many cases. Various empirical models were developed for describing the reaction kinetics during the pyrolysis of solid samples. Most of these models attempt to establish equations that will globally describe the kinetics of the process and fit the pyrolysis data. Several models of this type will be described in Section 3.3. A different approach can be chosen, mainly for uniform repetitive polymers. In such cases, a correct equation can be developed for the description of the reaction kinetics. This is based on the study of the steps occurring during pyrolysis involving a free radical chain mechanism. The subject will be discussed in some detail in Section 3.4. 

Otsu, T. Yoshida, M. Makromol. Chem. Rapid Commun. 1982, 3, 127. Otsu, T. Yoshida, M. Makromol. Chem. Rapid Commun. 1982, 3, 133. Otsu, T. Matsunaga, T. Kuriyama, A. Yoshioka, M. Eur. Polym. J. 1989, 25, 643, and references therein. In a lucid highlight, Prof. Otsu has recently reviewed his work and the iniferter technique. An iniferter is a compound the fragments of which Initiate and preferably cross-terminate by primary radical termination and which is subject to chain transfer from the propagating species, although for many of Otsu s examples chain transfer is unlikely. Otsu, T. J. Polym. Sci, Part A Polym. Chem. 2000, 38, 2121. 

While free-radical chain reactions were known shortly after the turn of the 20th century, it was not until the mid-1930s that free-radical polymerization was recognized. Today, free-radical polymerization finds application in the synthesis of many important classes of polymers including those based upon methacrylates, styrene, chloroprene, acrylonitrile, ethylene, and the many copolymers of these vinyl monomers. Many good reviews and books on this subject are available.12... 

The reaction of organic compounds with oxygen, known as autoxidation, is the most common of all organic reactions. The reaction is a free radical chain process involving peroxyl radicals which includes initiation, propagation and termination steps and is the subject of earlier reviews"". For control of these reactions under laboratory conditions, the reaction is usually initiated by azo initiators. The reactions are outlined briefly in equations 2-4. 

It was shown that the reaction involves a free radical chain process, subject to catalysis by peroxides and a, a -azobisisobutyronitrile, and inhibition by hydroquinone o). kinetic chain length of at least 7000 at 50 °C was estimated. 

When allylstannanes bearing an electron-withdrawing group were reacted with olefins and aromatic carbonyl compounds, with AIBN as radical-initiator, allylstan-nation occurred via radical chain process on the C=C and C=O double bonds, respectively [100]. On treatment of homochiral acrylates with a chiral auxihary on the carbonyl with an allylstannane in the presence of initiators such as AIBN and Et(B, the desired aUylstannation products were obtained with moderate to high diastereoselectivity (Scheme 12.38). When acetylenes were subjected to this procedure, aUylstannylation also occurred, leading preferentially to anti adducts. 

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