Organic peroxides
In organic chemistry, organic peroxides are organic compounds containing the peroxide functional group (R−O−O−R′). If the R′ is hydrogen, the compounds are called hydroperoxides, which are discussed in that article. The O−O bond of peroxides 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 polymerization, such as the acrylic, unsaturated polyester, and vinyl ester 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 explosively combust. Organic peroxides, like their inorganic counterparts, are often powerful bleaching agents.[1]
Types of organic peroxides
- Examples of organic peroxides
tert-Butyl hydroperoxide, a hydroperoxide (formula: ROOH) that is used to epoxide alkenes.
Dicumyl peroxide, a dialkyl peroxide (formula: ROOR) that is used to initiate polymerizations.
tert-butylperoxybenzoate, a peroxy ester (formula: RCO3R') that used as a radical initiator.
dibenzoyl peroxide, a diacyl peroxide (formula: (RCO2)2)) is also used as an initiator for polymerizations.
Peroxyacetic acid, a peroxycarboxylic acid (formula: (RCO3H), is a reagent in organic synthesis.
Organic peroxides are classified (i) by the presence or absence of a hydroxyl (-OH) terminus and (ii) by the presence of alkyl vs acyl substituents.[2] One gap in the classes of organic peroxides is diphenyl peroxide. Quantum chemical calculations predict that it undergoes a nearly barrierless reaction akin to the benzidine rearrangement.[3]
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.[4][5]
Biology
Peroxides play important roles in biology. Many aspects of biodegradation or aging are attributed to the formation and decay of peroxides formed from oxygen in air. Countering these effects is an array of biological and artificial antioxidants.
Hundreds of peroxides and hydroperoxides are known, being derived from fatty acids, steroids, and terpenes. Fatty acids form a number of 1,2-dioxenes. The biosynthesis prostaglandins proceeds via an endoperoxide, a class of bicyclic peroxides.[6] 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).[7]
Industrial uses
In polymer chemistry
Many peroxides are used as a radical initiators, e.g., to enable 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.[8] The polymerization rate is adjusted by suitable choice of temperature and type of peroxide.[9]
Methyl ethyl ketone peroxide, benzoyl peroxide and to a smaller degree acetone peroxide are used as initiators for radical polymerization of some thermosets, e.g. unsaturated polyester and vinyl ester, often encountered when making fiberglass or carbon fiber composites (CFRP).
Benzoyl peroxide, peroxyesters/peroxyketals, and alkylperoxy monocarbonates are used in production of polystyrene, expanded polystyrene, and High Impact Polystyrene, and benzoyl peroxide is utilized for many acrylate based adhesive applications.
Thermoplastic production techniques for many industrial polymerization applications include processes which are carried out in bulk, solution, or suspension type batches. Relevant polymers include polyvinyl chloride (PVC), low-density polyethylene (LDPE), polymethyl methacrylate (PMMA), and polystyrene.
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
Dialkyl peroxides, e.g., dicumyl peroxide, are synthesized by addition of hydrogen peroxide to alkenes or by O-alkylation of hydroperoxides.
Diacyl peroxides are typically prepared by treating hydrogen peroxide with acid chlorides or acid anhydrides in the presence of base:[1]
- H2O2 + 2 RCOCl → (RCO2)2 + 2 HCl
- H2O2 + (RCO)2O → (RCO2)2 + H2O
The reaction competes with hydrolysis of the acylating agent but the hydroperoxide anion is a superior nucleophile relative to hydroxide. Unsymmetrical diacyl peroxides can be produced by treating acyl chlorides with the peroxy acid.
Peresters, an example being tert-Butyl peroxybenzoate, are produced by treating acid anhydrides or acid chlorides with hydroperoxides.
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
Homolysis
Organic peroxides are widely used to initiate polymerization of olefins, e.g. the formation of polyethylene. A key step is homolysis:
- ROOR ⇌ 2 RO.
The tendency to homolyze is also exploited to 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).
Self-oxidation
Especially when in concentrated form, organic peroxides can decompose by self-oxidation, since organic peroxides contain both an oxidizer (the O-O bond) and fuel (C-H and C-C bonds). A "self-accelerating decomposition" occurs when the rate of peroxide decomposition generates 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).
Cumene process
Hydroperoxides are intermediates or reagents in major commercial processes. In the cumene process, acetone and phenol are produced by decomposition of cumene hydroperoxide (Me = methyl):
Reduction
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 → P(OR)3 + 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 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]
Analysis of peroxides
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]
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.
Safety
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 |
See also
External links
- Organic Peroxide Producers Safety Division
- OSH Answers – organic peroxides
- . carolina.com. Burlington, NC: Carolina Biological Supply Company. Archived from the original on 2007-12-18.
- Peroxide disposal
- European Organic Peroxide Safety Group
References
- ^ a b Klenk, Herbert; Götz, Peter H.; Siegmeier, Rainer; Mayr, Wilfried. "Peroxy Compounds, Organic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_199.pub2.
- ^ Saul Patai, ed. (1983). PATAI'S Chemistry of Functional Groups: Peroxides. Wiley. ISBN 9780470771730.
- ^ "Henry Rzepa's Blog: Why diphenyl peroxide does not exist".
- ^ 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.
- ^ 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.
- ^ D. A. Casteel (1992). "Peroxy Natural Products". Natural Product Reports. 9 (4): 289–312. doi:10.1039/np9920900289. PMID 1522977.
- ^ Aldo Roda Chemiluminescence and Bioluminescence: Past, Present and Future, p. 57, Royal Society of Chemistry, 2010, ISBN 1-84755-812-7
- ^ Thomas Brock, Michael Groteklaes, Peter Mischke Lehrbuch der Lacktechnologie, Vincentz Network GmbH & Co KG, 2000, ISBN 3-87870-569-7 p. 67
- ^ Organische Peroxide für die Polymerisation 2016-06-29 at the Wayback Machine. pergan.com (in German)
- ^ Criegee, Rudolf; Müller, Gerhard (1956). "1.2-Dioxan". Chemische Berichte. 89 (2): 238. doi:10.1002/cber.19560890209.
- ^ Heinz G. O. Becker Organikum, Wiley-VCH, 2001, ISBN 3-527-29985-8, p. 323
- ^ 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.
- ^ 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.
- ^ Légrádi, L.; Légrádi, J. (1970). "Detection of peroxides, hydroperoxides and peracids". Microchimica Acta. 58: 119–122. doi:10.1007/BF01218105. S2CID 101877371.
- ^ 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. Bibcode:1931RSPSB.108..175L. doi:10.1098/rspb.1931.0030.
- ^ Veibel, S. Analytik organischer Verbindungen, Akademie-Verlag, Berlin, 1960, p. 262
- ^ Eiss, M. I.; Giesecke, Paul (1959). "Colorimetric Determination of Organic Peroxides". Analytical Chemistry. 31 (9): 1558. doi:10.1021/ac60153a038.
- ^ 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.
- ^ Martin, A. J. (1957). "Potentiometric titration of hydroperoxide and peracid in Anhydrous Ethylenediamine". Analytical Chemistry. 29: 79–81. doi:10.1021/ac60121a022.
- ^ "ASTM E298, Standard Test Methods for Assay of Organic Peroxides". ASTM. 2010.
- ^ Heinz G. O. Becker Organikum, Wiley-VCH, 2001, ISBN 3-527-29985-8 pp. 741–762
- ^ Ozonelab Peroxide compatibility
- ^ "Product Stewardship". American Chemistry Council. 2021-01-17. Retrieved 2022-01-03.