Diphenylpicryl hydrazyl stable

In the paper published in 1900, he reported that hexaphenylethane (2) existed in an equilibrium mixture with 1. In 1968, the structure of the dimer of 1 was corrected to be l-diphenylmethylene-4-triphenylmethyl-2,5-cyclohexadiene 3, not 2 [38]. Since Gomberg s discovery, a number of stable radicals have been synthesized and characterized, e.g., triarylmethyls, phenoxyls, diphenylpicryl-hydrazyl and its analogs, and nitroxides [39-43]. The radical 1 is stable, if oxygen, iodine, and other materials which react easily with it are absent. Such stable radicals scarcely initiate vinyl polymerization, but they easily combine with reactive (short-lived) propagating radicals to form non-paramagnetic compounds. Thus, these stable radicals have been used as radical scavengers or polymerization inhibitors in radical polymerization. 

Boutevin et al. [177-180] treated different types of wastes of polyolefins (more often low density polyethylene) with a mixture air/ozone. They focused their studies on the quantification of the formed oxygenated species based on colorimetric titration using stable radicals such as diphenylpicryl-hydrazyl. They investigated the influence of mineral compounds (iron oxide, for example) used as catalysts for oxidative reactions. The ozonized polymers have been used as binders for composites materials containing mineral materials (sand, stones, etc.). 

An inhibitor is used to completely stop the conversion of monomer to polymer produced by accidental initiation during storage. To induce the inhibition, some stable radicals are mixed with the monomer. Such radicals are incapable for initiation the polymerization, but they are very effective in combining with any propagating radical. Diphenylpicryl-hydrazyl and tetramethylpiperidinyloxy (TEMPO) are two examples of radicals used to inhibit the radical polymerization. The chemical reactions of the inhibition produced by these compounds are shown in Scheme 4.8. 

The radicals corresponding to binaphthols possess substantially greater stability. Thus, in the oxidation of binaphthol (VI) and its oxy-derivative (VII), stable radicals are formed, characterized by triplet EPR spectra (Fig. 37). The triplet arises on account of the strong interaction of the unpaired electron only with the two equivalent protons of the rings (splitting 2. 7 Oe) the remaining protons interact weakly with the electron. The radicals are stable and do not react with diphenylpicryl-hydrazyl at room temperature however, they disproportionate rapidly under the action of light. 

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