Organic peroxide

Organic peroxides are organic compounds containing the peroxide functional group (ROOR′). If the R′ is hydrogen, the compounds are called organic hydroperoxides. Peresters have general structure RC(O)OOR. The O−O bond easily breaks, producing free radicals of the form RO• (the dot represents an unpaired electron). Thus, organic peroxides are useful as initiators for some types of polymerisation, such as the epoxy resins used in glass-reinforced plastics. MEKP and benzoyl peroxide are commonly used for this purpose. However, the same property also means that organic peroxides can either intentionally or unintentionally initiate explosive polymerisation in materials with unsaturated chemical bonds, and this process has been used in explosives. Organic peroxides, like their inorganic counterparts, are powerful bleaching agents.[1]

A bridging peroxide group in ascaridole.
Chondrillin is one of several naturally occurring 1,2-dioxenes.
Prostaglandin H2, an endoperoxide (cyclic peroxide), is a precursor to other prostaglandins.
The general structure of an organic peroxide
The general structure of a perester

Properties

The O−O bond length in peroxides is about 1.45 Å, and the R−O−O angles (R = H, C) are about 110° (water-like). Characteristically, the C−O−O−R (R = H, C) dihedral angles are about 120°. The O−O bond is relatively weak, with a bond dissociation energy of 45–50 kcal/mol (190–210 kJ/mol), less than half the strengths of C−C, C−H, and C−O bonds.[2][3]

Major classes of organic peroxides include:

  • hydroperoxides, compounds with the functionality ROOH (R = alkyl).
  • peroxy acids and esters, compounds with the functionality RC(O)OOH and RC(O)OOR' (R,R' = alkyl, aryl).
  • diacyl peroxides, compounds with the functionality RC(O)OOC(O)R (R = alkyl, aryl).
  • dialkylperoxides, compounds with the functionality ROOR (R = alkyl).

These compounds occur in nature or are useful in commercial settings. Still other more specialized peroxy compounds are known.[4]

Biology

Peroxides play important roles in biology. Hundreds of peroxides and hydroperoxides are known, being derived from fatty acids, steroids, and terpenes. Derived from fatty acids are a number of 1,2-dioxenes. The biosynthesis prostaglandins proceeds via an endoperoxide, a class of bicyclic peroxides.[5] In fireflies, oxidation of luciferins, which is catalyzed by luciferases, yields a peroxy compound 1,2-dioxetane. The dioxetane is unstable and decays spontaneously to carbon dioxide and excited ketones, which release excess energy by emitting light (bioluminescence).[6]

Loss of CO2 of a dioxetane, giving rise to an excited ketone, which relaxes by emitting light.
Firefly Lampyris noctiluca

Industrial uses

In polymer chemistry

Dibenzoyl peroxide is used as a radical initiator and to assist polymerization of acrylates. Industrial resins based on acrylic and/or methacrylic acid esters are invariably produced by radical polymerization with organic peroxides at elevated temperatures.[7] The polymerization rate is adjusted by suitable choice of temperature and type of peroxide.[8]

Methyl ethyl ketone peroxide, benzoyl peroxide and to a smaller degree acetone peroxide are used as initiators for radical polymerisation of some resins, e.g. polyester and silicone, often encountered when making fiberglass. Pinane hydroperoxide is used in production of styrene-butadiene (synthetic rubber).

Bleaching and disinfecting agents

Benzoyl peroxide and hydrogen peroxide are used as bleaching and "maturing" agents for treating flour to make its grain release gluten more easily; the alternative is letting the flour slowly oxidize by air, which is too slow for the industrialized era. Benzoyl peroxide is an effective topical medication for treating most forms of acne.

Preparation

From hydrogen peroxide

Dialkylsulfates react with alkaline hydrogen peroxide.[9] In this method, the alkyl sulfate donates the alkyl group and the sulfate ion forms the leaving group:

This method can also yield cyclic peroxides.[10] The four-membered dioxetanes can be obtained by 2+2 cycloaddition of oxygen to alkenes.[11]

Reactions

Organoperoxides can be reduced to alcohols with lithium aluminium hydride, as described in this idealized equation:

4 ROOH + LiAlH4 → LiAlO2 + 2 H2O + 4 ROH

The phosphite esters and tertiary phosphines also effect reduction:

ROOH + PR3 → OPR3 + ROH

Cleavage to ketones and alcohols in the base catalyzed Kornblum–DeLaMare rearrangement

Some peroxides are drugs, whose action is based on the formation of radicals at desired locations in the organism. For example, artemisinin and its derivatives, such as such artesunate, possess the most rapid action of all current drugs against falciparum malaria.[12] Artesunate is also efficient in reducing egg production in Schistosoma haematobium infection.[13]

Iodine-starch test. Note the blackening (left) of initially yellowish (right) starch.

Several analytical methods are used for qualitative and quantitative determination of peroxides.[14] A simple qualitative detection of peroxides is carried out with the iodine-starch reaction.[15] Here peroxides, hydroperoxides or peracids oxidize the added potassium iodide into iodine, which reacts with starch producing a deep-blue color. Commercial paper indicators using this reaction are available. This method is also suitable for quantitative evaluation, but it can not distinguish between different types of peroxide compounds. Discoloration of various indigo dyes in presence of peroxides is used instead for this purpose.[16] For example, the loss of blue color in leuco-methylene blue is selective for hydrogen peroxide.[17]

Quantitative analysis of hydroperoxides can be performed using potentiometric titration with lithium aluminium hydride.[18] Another way to evaluate the content of peracids and peroxides is the volumetric titration with alkoxides such as sodium ethoxide.[19]

Active oxygen in peroxides

Each peroxy group is considered to contain one active oxygen atom. The concept of active oxygen content is useful for comparing the relative concentration of peroxy groups in formulations, which is related to the energy content. In general, energy content increases with active oxygen content, and thus the higher the molecular weight of the organic groups, the lower the energy content and, usually, the lower the hazard.

The term active oxygen is used to specify the amount of peroxide present in any organic peroxide formulation. One of the oxygen atoms in each peroxide group is considered "active". The theoretical amount of active oxygen can be described by the following equation:[20]

A[O]theoretical (%) = 16p/m × 100,

where p is the number of peroxide groups in the molecule, and m is the molecular mass of the pure peroxide.

Organic peroxides are often sold as formulations that include one or more phlegmatizing agents. That is, for safety sake or performance benefits the properties of an organic peroxide formulation are commonly modified by the use of additives to phlegmatize (desensitize), stabilize, or otherwise enhance the organic peroxide for commercial use. Commercial formulations occasionally consist of mixtures of organic peroxides, which may or may not be phlegmatized.

Thermal decomposition of organic peroxides

Organic peroxides are useful in chemical synthesis due to their propensity to decompose. In doing so they generate useful radicals that can initiate polymerization to create polymers, modify polymers by grafting or visbreaking, or cross-link polymers to create a thermoset. When used for these purposes, the peroxide is highly diluted, so the heat generated by the exothermic decomposition is safely absorbed by the surrounding medium (e.g. polymer compound or emulsion). But when a peroxide is in a more pure form, the heat evolved by its decomposition may not dissipate as quickly as it is generated, which can result in increasing temperature, which further intensifies the rate of exothermic decomposition. This can create a dangerous situation known as a self-accelerating decomposition.

A self-accelerating decomposition occurs when the rate of peroxide decomposition is sufficient to generate heat at a faster rate than it can be dissipated to the environment. Temperature is the main factor in the rate of decomposition. The lowest temperature at which a packaged organic peroxide will undergo a self-accelerating decomposition within a week is defined as the self-accelerating decomposition temperature (SADT).

Safety
The GHS transport pictogram for organic peroxides.

Peroxides are also strong oxidizers and easily react with skin, cotton and wood pulp.[21] For safety reasons, peroxidic compounds are stored in a cool, opaque container, as heating and illumination accelerate their chemical reactions. Small amounts of peroxides, which emerge from storage or reaction vessels are neutralized using reducing agents such as iron(II) sulfate. Safety measures in industrial plants producing large amounts of peroxides include the following:

1) The equipment is located within reinforced concrete structures with foil windows, which would relieve pressure and not shatter in case of explosion.

2) The products are bottled in small containers and are moved to a cold place promptly after the synthesis.

3) The containers are made of non-reactive materials such as stainless steel, some aluminium alloys or dark glass.[22]

For safe handling of concentrated organic peroxides, an important parameter is temperature of the sample, which should be maintained below the self accelerating decomposition temperature of the compound.[23]

The shipping of organic peroxides is restricted. The US Department of Transportation lists organic peroxide shipping restrictions and forbidden materials in 49 CFR 172.101 Hazardous Materials Table based on the concentration and physical state of the material:

Chemical name CAS Number Prohibitions
Acetyl acetone peroxide 37187-22-7 > 9% by mass active oxygen
Acetyl benzoyl peroxide 644-31-5 solid, or > 40% in solution
Ascaridole 512-85-6 (organic peroxide)
tert-Butyl hydroperoxide 75-91-2 > 90% in solution (aqueous)
Di-(1-naphthoyl)peroxide 29903-04-6
Diacetyl peroxide 110-22-5 solid, or > 25% in solution
Ethyl hydroperoxide 3031-74-1
Iodoxy compounds dry
Methyl ethyl ketone peroxide 1338-23-4 > 9% by mass active oxygen in solution
Methyl isobutyl ketone peroxide 37206-20-5 > 9% by mass active oxygen in solution
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See also
  • OSH Answers – organic peroxides
  • "The Perils of Peroxides". carolina.com. Burlington, NC: Carolina Biological Supply Company. Archived from the original on 2007-12-18.
  • Peroxide disposal
  • Organic Peroxide Producers Safety Division. Oct. 2011. The Society of the Plastics Industry. 24 Oct. 2011.

References
  1. Klenk, Herbert; Götz, Peter H.; Siegmeier, Rainer; Mayr, Wilfried. "Peroxy Compounds, Organic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH.
  2. Bach, Robert D.; Ayala, Philippe Y.; Schlegel, H. B. (1996). "A Reassessment of the Bond Dissociation Energies of Peroxides. An ab Initio Study". J. Am. Chem. Soc. 118 (50): 12758–12765. doi:10.1021/ja961838i.
  3. Otto Exner (1983). "Stereochemical and conformational aspects of peroxy compounds". In Saul Patai (ed.). PATAI'S Chemistry of Functional Groups. Wiley. pp. 85–96. doi:10.1002/9780470771730.ch2. ISBN 9780470771730.
  4. Saul Patai, ed. (1983). PATAI'S Chemistry of Functional Groups: Peroxides. Wiley. ISBN 9780470771730.
  5. D. A. Casteel (1992). "Peroxy Natural Products". Natural Product Reports. 9 (4): 289–312. doi:10.1039/np9920900289.
  6. Aldo Roda Chemiluminescence and Bioluminescence: Past, Present and Future, p. 57, Royal Society of Chemistry, 2010, ISBN 1-84755-812-7
  7. Thomas Brock, Michael Groteklaes, Peter Mischke Lehrbuch der Lacktechnologie, Vincentz Network GmbH & Co KG, 2000, ISBN 3-87870-569-7 p. 67
  8. Organische Peroxide für die Polymerisation Archived 2016-06-29 at the Wayback Machine. pergan.com (in German)
  9. Medwedew, S. S.; Alexejewa, E. N. (1932). "Organic peroxides II. Of the reaction between benzoyl hydroperoxide or benzoyl peroxide and triphenylmethyl". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 65 (2): 137. doi:10.1002/cber.19320650204.
  10. Criegee, Rudolf; Müller, Gerhard (1956). "1.2-Dioxan". Chemische Berichte. 89 (2): 238. doi:10.1002/cber.19560890209.
  11. Heinz G. O. Becker Organikum, Wiley-VCH, 2001, ISBN 3-527-29985-8, p. 323
  12. White NJ (1997). "Assessment of the pharmacodynamic properties of antimalarial drugs in vivo". Antimicrob. Agents Chemother. 41 (7): 1413–22. doi:10.1128/AAC.41.7.1413. PMC 163932. PMID 9210658.
  13. Boulangier D, Dieng Y, Cisse B, et al. (2007). "Antischistosomal efficacy of artesunate combination therapies administered as curative treatments for malaria attacks". Trans R Soc Trop Med Hyg. 101 (2): 113–16. doi:10.1016/j.trstmh.2006.03.003. PMID 16765398.
  14. Légrádi, L.; Légrádi, J. (1970). "Detection of peroxides, hydroperoxides and peracids". Microchimica Acta. 58: 119–122. doi:10.1007/BF01218105.
  15. Lea, C. H. (1931). "The Effect of Light on the Oxidation of Fats". Proceedings of the Royal Society B: Biological Sciences. 108 (756): 175–189. doi:10.1098/rspb.1931.0030.
  16. Veibel, S. Analytik organischer Verbindungen, Akademie-Verlag, Berlin, 1960, p. 262
  17. Eiss, M. I.; Giesecke, Paul (1959). "Colorimetric Determination of Organic Peroxides". Analytical Chemistry. 31 (9): 1558. doi:10.1021/ac60153a038.
  18. Higuchi, T.; Zuck, Donald Anton (1951). "Behaviors of Several Compounds as Indicators in Lithium Aluminum Hydride Titration of Functional Groups". Journal of the American Chemical Society. 73 (6): 2676. doi:10.1021/ja01150a073.
  19. Martin, A. J. (1957). "Potentiometric titration of hydroperoxide and peracid in Anhydrous Ethylenediamine". Analytical Chemistry. 29: 79–81. doi:10.1021/ac60121a022.
  20. "ASTM E298, Standard Test Methods for Assay of Organic Peroxides". ASTM. 2010.
  21. Heinz G. O. Becker Organikum, Wiley-VCH, 2001, ISBN 3-527-29985-8 pp. 741–762
  22. Ozonelab Peroxide compatibility
  23. Organic Peroxide Producers Safety Division (2012-08-06). "Safety and Handling of Organic Peroxides" (PDF). The Society of the Plastics Industry, Inc. Archived from the original (PDF) on 2013-06-20. Retrieved 2012-10-03.
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