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Termination decomposition

An alternative chain-terminating decomposition of the tetroxide, known as the Russell mechanism (29), can occur when there is at least one hydrogen atom in an alpha position the products are a ketone, an alcohol and oxygen (eq. 15). This mechanism is troubling on theoretical grounds (1). Questions about its vaUdity remain (30), but it has received some recent support (31). [Pg.335]

Mineralization of organic macromolecules is initiated by extracellular enzymes because bacteria are unable to hydrolyze substrates that are much larger than about 600 Da (Weiss et al., 1991). Not all bacteria are capable of synthesizing these enzymes, as is often the case with those responsible for terminal decomposition and some intermediary metabolisms. As a result, these terminal organisms depend heavily on the activities of other bacteria for substrates. It is clear that polymer hydrolysis occurs since these compounds are required to support microbial activities in sediments, but some studies have failed to detect polymer hydrolysis potentials sufficient to support in situ rates of metabolism (Arnosti, 1998). Such studies underscore the difficulties of examining hydrolytic processes. [Pg.4190]

Reduction of derivatives of estradiol 3-methyl ether (I) and hydrolysis of the initially formed enol ether II provides an efficient route to 19-norsteroids (111) of considerable importance in hormone therapy. A. J. Birch, who introduced the method (1949), used sodium in liquid ammonia with ethanol as proton donor. A. L. Wilds and N.A. Nelson (1953) found that yields are improved by use of lithium in place of sodium and that lithium is effective in some cases where sodium is not. The Wilds-Nelson procedure, which became the standard one, employs ether as co-solvent and involves adding the ethanol lust terminal decomposition is done with water after evaporation of ammonia, Since this reaction is the key step in processes developed by O. D. Searleand Co. for the production of two I V-norsteroids... [Pg.30]

New radicals are introduced by thermolysis of the hydroperoxide by chain-branching decomposition (eq. 4). Radicals are removed from the system by chain-termination reaction(s) (eq. 5). Under steady-state conditions, the production of new radicals is in balance with the rate of radical removal by termination reactions and equation 8 appHes for the scheme of equations 1—5 where r. = rate of new radical introduction (eq. 4). [Pg.334]

One decomposition of the tetioxide is not terminating, producing alkoxy radicals and oxygen (eq. 14). [Pg.335]

Modem real time instmmental methods permit analyses of unstable transient species and the free-radical intermediates as well. These methods have gready expanded the scope and power of VPO studies, but important basic questions remain unresolved. Another complication is the role of surface. Peroxide decompositions and radical termination reactions can occur on a surface so that, depending on circumstances, surfaces can have either an inhibiting or accelerating effect. Each surface has varying amounts of adventitious contaminants and also accumulates deposits during reaction. Thus no two surfaces are exactly alike and each changes with time. [Pg.338]

Although primary and secondary alkyl hydroperoxides are attacked by free radicals, as in equations 8 and 9, such reactions are not chain scission reactions since the alkylperoxy radicals terminate by disproportionation without forming the new radicals needed to continue the chain (53). Overall decomposition rates are faster than the tme first-order rates if radical-induced decompositions are not suppressed. [Pg.103]

Propagation. Propagation reactions (eqs. 5 and 6) can be repeated many times before termination by conversion of an alkyl or peroxy radical to a nonradical species (7). Homolytic decomposition of hydroperoxides produced by propagation reactions increases the rate of initiation by the production of radicals. [Pg.223]

Autoca.ta.Iysis. The oxidation rate at the start of aging is usually low and increases with time. Radicals, produced by the homolytic decomposition of hydroperoxides and peroxides (eqs. 2—4) accumulated during the propagation and termination steps, initiate new oxidative chain reactions, thereby increasing the oxidation rate. [Pg.223]

Regarding a historical perspective on carbon nanotubes, very small diameter (less than 10 nm) carbon filaments were observed in the 1970 s through synthesis of vapor grown carbon fibers prepared by the decomposition of benzene at 1100°C in the presence of Fe catalyst particles of 10 nm diameter [11, 12]. However, no detailed systematic studies of such very thin filaments were reported in these early years, and it was not until lijima s observation of carbon nanotubes by high resolution transmission electron microscopy (HRTEM) that the carbon nanotube field was seriously launched. A direct stimulus to the systematic study of carbon filaments of very small diameters came from the discovery of fullerenes by Kroto, Smalley, and coworkers [1], The realization that the terminations of the carbon nanotubes were fullerene-like caps or hemispheres explained why the smallest diameter carbon nanotube observed would be the same as the diameter of the Ceo molecule, though theoretical predictions suggest that nanotubes arc more stable than fullerenes of the same radius [13]. The lijima observation heralded the entry of many scientists into the field of carbon nanotubes, stimulated especially by the un-... [Pg.36]

The ratio of terminal to internal alkene from decomposition of some sulfonhun salts under alkaline conditions is as indicated ... [Pg.402]

Polyethylene is the simplest of so-called high polymers. The reaction for low density polyethylene (LDPE) follows the classical free radical polymerization steps of initiator decomposition, initiation, propagation, and termination. The reaction is... [Pg.233]

Thermal decomposition of LiR eliminates a /6-hydrogen atom to give an olefin and LiH, a process of industrial importance for long-chain terminal alkenes. Alkenes can also be produced by treatment of ethers, the organometallic reacting here as a very strong base (proton acceptor) ... [Pg.105]

Terminal acetylenes can be obtained from the corresponding propylcarboxylic acids by thermal decomposition. Thus, l-methyl-3-ethynyl- and 2-methyl-3-ethynylindazole were obtained by thermolysis of indazolylpropiolic acids at 150-160°C. Yields of ethynyl derivatives were 65 and 60%, respectively (75KGS1678) (Scheme 100 Table XXIII). [Pg.48]

The departure of dependence of Rp on the concentration of CHP from 0.5 order might be ascribed to induction decomposition of ROOH type to form ROO- radical, which has very low activity to initiate monomer polymerization [40], but can combine with the propagation chain radical to form the primary radical termination. For the same reason, the order of concentration of TBH was also lower than 0.5 when the TBH-DMT system was used as the initiator in MMA bulk polymerization. But in the BPO-DMT initiation system as shown in Table... [Pg.232]

The OH radical formed during the decomposition of hydroperoxy groups is very reactive and can either terminate a reaction (39) or may attack the weak bond of the backbone polymer resulting in the formation of a new radical (40). [Pg.493]

The thermal (or photochemical) decomposition of the azo group gives rise to a radically initiated polymerization. The reactive site F, the transformation site, however, can, depending on its chemical nature, initiate a condensation or addition type reaction. It can also start radical or ionic polymerizations. F may also terminate a polymerization or even enable the azo initiator to act as a monomer in chain polymerizations. [Pg.735]

The introduction of chlorinated porphyrins (10) allowed for hydrogen peroxide to be used as terminal oxidant [62], These catalysts, discovered by Mansuy and coworkers, were demonstrated to resist decomposition, and efficient epoxidations of olefins were achieved when they were used together with imidazole or imidazo-lium carboxylates as additives, (Table 6.6, Entries 1 and 2). [Pg.201]

The second major discovery regarding the use of MTO as an epoxidation catalyst came in 1996, when Sharpless and coworkers reported on the use of substoichio-metric amounts of pyridine as a co-catalyst in the system [103]. A change of solvent from tert-butanol to dichloromethane and the introduction of 12 mol% of pyridine even allowed the synthesis of very sensitive epoxides with aqueous hydrogen peroxide as the terminal oxidant. A significant rate acceleration was also observed for the epoxidation reaction performed in the presence of pyridine. This discovery was the first example of an efficient MTO-based system for epoxidation under neutral to basic conditions. Under these conditions the detrimental acid-induced decomposition of the epoxide is effectively avoided. With this novel system, a variety of... [Pg.211]


See other pages where Termination decomposition is mentioned: [Pg.4189]    [Pg.125]    [Pg.4189]    [Pg.125]    [Pg.142]    [Pg.531]    [Pg.384]    [Pg.101]    [Pg.505]    [Pg.481]    [Pg.80]    [Pg.342]    [Pg.437]    [Pg.465]    [Pg.85]    [Pg.9]    [Pg.684]    [Pg.918]    [Pg.353]    [Pg.148]    [Pg.100]    [Pg.400]    [Pg.486]    [Pg.742]    [Pg.186]    [Pg.23]    [Pg.25]    [Pg.187]    [Pg.195]    [Pg.201]    [Pg.207]    [Pg.215]    [Pg.219]    [Pg.222]   
See also in sourсe #XX -- [ Pg.416 , Pg.426 ]




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Hydrogen peroxide decomposition chain terminating reactions

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