Dibenzoyl peroxide, initiator

Dihydrotagetone (95) has been synthesized by dibenzoyl peroxide-initiated radical reaction of 3-methylbutanal (80) and the diethyl acetal (96) of methacrolein the product 97 (obtained in 42% yield) could be converted conventionally to dihydrotagetone (95). The same author has described the direct radical addition of 82 to 3-methyl-3-butenyl acetate. The product, 98, in this case was deacetylated by pyrolysis over ceramic beads to dihydrotagetone (95). ... 

Benzotropilidenes. Swenton and Madigan have developed a general route to 3,4-benzotropilidenes that employs mUd, neutral conditions, which are essential to avoid isomerization to the more stable 1,2-isomer. The method is illustrated for the synthesis of 7-carbomethoxy-3,4-benzotropilidene (4). Copper sulfate catalyzed reaction of ethyl diazoacetate with 1,4-dihydronaphthalene (1) leads to the expected adduct, exo-7-carboethoxy-3,4-benzo[4.1.0]heptane, which is hydrolyzed and then esterified with methanol to give the corresponding methyl ester (2). This product is dibrominated (dibenzoyl peroxide initiation). The crude dibromide (3) is then refluxed in THF containing a trace of... 

Feng [344] has described the dibenzoyl peroxide-initiated polymerization of t-butyl vinyl ketone to an amorphous polymer in organic solvents, while several alkyl vinyl ketones have been polymerized in aqueous solutions to low-melting polymers using a potassium persulfate/sodium metabisulfite initiation [345]. Phenyl vinyl ketone was polymerized in an emulsion containing 7.5% soap and 0.2% potassium peroxodisulfate [346]. 

The extent of decarboxylation primarily depends on temperature, pressure, and the stabihty of the incipient R- radical. The more stable the R- radical, the faster and more extensive the decarboxylation. With many diacyl peroxides, decarboxylation and oxygen—oxygen bond scission occur simultaneously in the transition state. Acyloxy radicals are known to form initially only from diacetyl peroxide and from dibenzoyl peroxides (because of the relative instabihties of the corresponding methyl and phenyl radicals formed upon decarboxylation). Diacyl peroxides derived from non-a-branched carboxyhc acids, eg, dilauroyl peroxide, may also initially form acyloxy radical pairs however, these acyloxy radicals decarboxylate very rapidly and the initiating radicals are expected to be alkyl radicals. Diacyl peroxides are also susceptible to induced decompositions ... 

Aromatic diacyl peroxides such as dibenzoyl peroxide (BPO) [94-36-0] may be used with promoters to lower the usehil decomposition temperatures of the peroxides, although usually with some sacrifice to radical generation efficiency. The most widely used promoter is dimethylaniline (DMA). The BPO—DMA combination is used for hardening (curing) of unsaturated polyester resin compositions, eg, body putty in auto repair kits. Here, the aromatic amine promoter attacks the BPO to initially form W-benzoyloxydimethylanilinium benzoate (ion pair) which subsequentiy decomposes at room temperature to form a benzoate ion, a dimethylaniline radical cation, and a benzoyloxy radical that, in turn, initiates the curing reaction (33) ... 

To a solution of 279 g of o-chloroacetophenone in 2 liters of anhydrous diethyl ether were added about 3 g of dibenzoyl peroxide. 5 g of bromine were added to the resulting solution, and after 3 minutes, the color of bromine had been discharged, indicating that the formation of oj-bromo-o-chloroacetophenone had been initiated. A further amount of 288 g of bromine was added dropwise to the reaction mixture over a VA hour interval. After the addition of the bromine had been completed, the reaction mixture was stirred for one-half hour and poured over about 1 kg of crushed ice. 

The free-radical reaction may be equally initiated by photoactivated sulfur dioxide (3S02)442 (equation 79). On the other hand, polysulfones are obtained by radical copolymerization of appropriate olefins with sulfur dioxide443-449, and similarly, uptake of sulfur dioxide by a radical-pair formed by nitrogen extrusion from an azo compound yields the corresponding sulfone450 (equation 80). Correspondingly, alkylbenzenes, dibenzoyl peroxide, and sulfur dioxide yield sulfones under thermal conditions451... 

Basically, three reactions were evoked to support the occurrence of 5a-C-centered radicals 10 in tocopherol chemistry. The first one is the formation of 5a-substituted derivatives (8) in the reaction of a-tocopherol (1) with radicals and radical initiators. The most prominent example here is the reaction of 1 with dibenzoyl peroxide leading to 5a-a-tocopheryl benzoate (11) in fair yields,12 so that a typical radical recombination mechanism was postulated (Fig. 6.6). Similarly, low yields of 5a-alkoxy-a-tocopherols were obtained by oxidation of a-tocopherol with tert-butyl hydroperoxide or other peroxides in inert solvents containing various alcohols,23 24 although the involvement of 5 a-C-centered radicals in the formation mechanism was not evoked for explanation in these cases. 

At pressures above 6000 bar, free radical polymerisation sometimes proceeded explosively [ 1 ]. The parameters were determined in a batch reactor for thermal runaway polymerisation of acrylonitrile initiated by azoisobutyronitrile, dibenzoyl peroxide or di-/er/-butyl peroxide [2],... 

Biesenberg, J. S. etal., J. Polym. Eng. Sci., 1976,16, 101-116 Polymerisation of methyl methacrylate initiated by oxygen or peroxides proceeds with a steady increase in velocity during a variable induction period, at the end of which a violent 90°C exotherm occurs. This was attributed to an increase in chain branching, and not to a decrease in heat transfer arising from the increasing viscosity [ 1 ]. The parameters were determined in a batch reactor for thermal runaway polymerisation of methyl methacrylate, initiated by azoisobutyronitrile, dibenzoyl peroxide or di-ferf-butyl peroxide [2],... 

Sebastian, D. H. et al., Polym. Eng. Sci., 1976, 16, 117-123 The conditions were determined for runaway/non-runaway polymerisation of styrene in an oil-heated batch reactor at 3 bar, using dibenzoyl peroxide as initiator at 3 concentrations. Results are presented diagrammatically. 

The dry material is readily ignited, bums very rapidly and is moderately sensitive to heat, shock, friction or contact with combustible materials. When heated above its m.p. (103-105°C), instantaneous and explosive decomposition occurs without flame, but the decomposition products are flammable. If under confinement (or in large bulk), decomposition may be violently explosive [1], An explosion which occurred when a screw-capped bottle of the peroxide was opened was attributed to friction initiating a mixture of peroxide and organic dust in the cap threads [2], Waxed paper tubs are recommended to store this and other sensitive solids [3], Crystallisation of the peroxide from hot chloroform solution involves a high risk of explosion. Precipitation from cold chloroform solution by methanol is safer [4], Water- or plasticiser-containing pastes of dibenzoyl peroxide are much safer for industrial use. 

Some initiators, for example, AIBN (azobisisobutyronitrile) and dibenzoyl peroxide exhibit a strong quenching effect. That is why, the dependence of the CL intensity on the initiator concentration (/=r Vi) is nonlinear in these cases. 

According to this scheme, the intensity of CL is proportional to the rate of initiation (j/j) and depends on the concentrations of quenchers and activators. Some initiators, for example AIBN and dibenzoyl peroxide, act as strong quenchers [221] ... 

The initiators which are commonly used in these reactions range from azo-bis-isobutyronitrile (AIBN) to organic peroxides such as dibenzoyl peroxide, to ultra-violet light. In some cases, the reaction has been done with two different initiators42. A few illustrative examples of this reaction are presented in equations 57-59. 

Propynol, Mercury(II) sulfate, Sulfuric acid, Water, 4479 Styrene, Air, Polymerising styrene, 2945 Styrene, Butyllithium, 2945 Styrene, Dibenzoyl peroxide, 2945 Styrene, Initiators, 2945 f Tetrafluoroethylene, 0628... 

Peroxides are used when the reaction requires a more reactive initiating species. Thermolysis of dibenzoyl peroxide [PhC(0)0—OC(0)Ph], with a ti/2 of 1 h at 95 °C and 7 h at 70 °C, is the most familiar to synthetic chemists. It initially produces acyloxyl radicals that often decarboxylate prior to undergoing bimolecular reactions and affording the equally reactive phenyl radicals. 

The reduction of thiocarbonyl derivatives by EtsSiH can be described as a chain process under forced conditions (Reaction 4.50) [89,90]. Indeed, in Reaction (4.51) for example, the reduction of phenyl thiocarbonate in EtsSiD as the solvent needed 1 equiv of dibenzoyl peroxide as initiator at 110 °C, and afforded the desired product in 91 % yield, where the deuterium incorporation was only 48% [90]. Nevertheless, there are some interesting applications for these less reactive silanes in radical chain reactions. For example, this method was used as an efficient deoxygenation step (Reaction 4.52) in the synthesis of 4,4-difluoroglutamine [91]. 1,2-Diols can also be transformed into olefins using the Barton-McCombie methodology. Reaction (4.53) shows the olefination procedure of a bis-xanthate using EtsSiH [89]. 

Homolytic cleavage of most a bonds may be achieved if the compound is subjected to a sufficiently high temperature, typically about 200 °C. However, some weak bonds will undergo homolysis at temperatures little above room temperature. Bonds of peroxy and azo compounds fall in this category, and such compounds may be used to initiate a radical process. Di-tert-butyl peroxide, dibenzoyl peroxide... 

The kinetic relationship, according to which the rate of polymerization increases and the average degree of polymerization decreases with increasing initiator concentration, is satisfied by most monomers when either unsubstituted or substituted dibenzoyl peroxides are used as initiators. 

It must be emphasized that, in contrast to the initiation of polymerization with peroxo compounds or azo compounds, not every redox system is suitable for initiating polymerization of every unsaturated monomer. Before attempting to polymerize a new compound with a redox system it is, therefore, advisable first to test its radical polymerizability with dibenzoyl peroxide. 

Most emulsion polymerizations are performed with water-soluble initiators however, the following experiment describes a redox polymerization where one component (dibenzoyl peroxide) is water-insoluble, while the other is water-soluble. 

In the polymerization of acrylic monomers by bulk, suspension, or in organic solution, the most common initiators are diacyl peroxide (e.g., dibenzoyl peroxide supplied as a paste in water) or azo compounds (e.g., 2,2 -azobisisobutyronitrile). For emulsion or aqueous solution polymerizations, sodium persulfate by itself or in combination with bisulfites or a host of other reducing agents may be used. 

Initiators commonly used include dibenzoyl peroxide, lauryl peroxide, 2, 2 -azobis isobutyronitrile, and others that are suitable for use in the temperature range of approximately 60-90°C. 

With sensitizers, initiation stops when the source of radiation is turned off, which is followed by a rapid decay of the polymerization process. When a conventional initiator, such as dibenzoyl peroxide, is also present, the process is more rapid than when the sensitizer is used by itself. It also seems to continue after the radiation source has been discontinued. It is presumed that ultraviolet (UV)-induced decomposition of the peroxide becomes involved in the process. By this method, polymerizations may be carried out at temperatures well below those normally used with thermal initiators such as organic peroxides. 

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