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Vinylene carbonate

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Vinylene carbonate
Names
IUPAC name
1,3-dioxol-2-one
Other names
1,3-Dioxolene-2-one
Vinyl carbonate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.011.659 Edit this at Wikidata
EC Number
  • 212-825-5
  • InChI=1S/C3H2O3/c4-3-5-1-2-6-3/h1-2H
    Key: VAYTZRYEBVHVLE-UHFFFAOYSA-N
  • C1=COC(=O)O1
Properties
C3H2O3
Molar mass 86.05 g·mol−1
Appearance colourless liquid[1]
Density 1.35
Melting point 22 °C (72 °F; 295 K)
Boiling point 178 °C (352 °F; 451 K) [2]
Hazards
GHS labelling:
GHS05: CorrosiveGHS06: ToxicGHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard
Danger
H302, H311, H315, H317, H318, H373, H411
P260, P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P305+P351+P338, P310, P312, P314, P321, P322, P330, P332+P313, P333+P313, P361, P362, P363, P391, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Vinylene carbonate (VC) or 1,3-dioxol-2-one, is the simplest unsaturated cyclic carbonic acid ester. Vinylene carbonate can also be thought of as the cyclic carbonate of the hypothetical (Z)-ethene-1,2-diol. The activated double bond in this five-membered oxygen-containing heterocycle makes the molecule a reactive monomer for homopolymerization and copolymerization and a dienophile in Diels-Alder reactions. Below room temperature vinylene carbonate is a colorless stable solid.

Preparation

Since its first description in 1953,[3] ethylene carbonate has been commonly used as starting material for vinylene carbonate. In the first stage, monochlorethylene carbonate is produced in a UV-initiated photochlorination reaction with chlorine or sulfuryl chloride at 60-70 °C in bulk. In the second stage, monochlorethylene is converted in a dehydrochlorination reaction (e.g. with triethylamine) at 40-60 °C into vinylene carbonate. The reaction mixture can optionally be diluted with ethylene carbonate,[4] vinylene carbonate[5] or methyl tert-butyl ether.[6]

Vinylencarbonat-Synthese

Instead of in the liquid phase, the dehydrochlorination may also be carried out in the gas phase on a zinc chloride impregnated catalyst in a fluidized bed reactor at 350-500 °C with average yields of 69%.[7] The seemingly simple reaction yields only 70 to 80% of impure end product due to a variety of side reactions. For example, in the chlorination of ethylene carbonate in substance or solution, 2-chloroacetaldehyde, polychlorinated ethylene carbonate and chlorinated ring-opening products are formed besides others. The separation of the by-products from the final product by distillation by thin-film evaporator,[4] fractional recrystallization[8] or zone melting[9] is very expensive. The content of by-products can be reduced by stirring with sodium borohydride[10] or urea[11] at elevated temperature. However, the purification is complicated by the pronounced thermolability of vinylene carbonate, as it decomposes at temperatures above 80 °C within minutes.[4] Highly pure vinylene carbonate can be obtained in yields of more than 70% by optimizing the chlorination conditions to suppress the formation of by-products[6] and a combination of several gentle purification processes.[12] The tendency of the liquid vinylene carbonate to polymerize is suppressed by addition of inhibitors such as butylhydroxytoluene (BHT).

Properties

Industrially produced vinylene carbonate is usually a yellow to brown liquid. By suitable process control and purification steps, a solid product with a melting point of 20-22 °C and a chlorine content below 10ppm can be obtained. Liquid vinylene carbonate turns rapidly yellow even in the absence of light and must be stabilized by the addition of radical scavengers. In solid form, the highly pure substance is long-term stable when stored below 10 °C.[13] Vinylene carbonate dissolves in a variety of solvents such as ethanol, tetrahydrofuran, ethylene carbonate, propylene carbonate, and other dipolar aprotic electrolyte solvents used for lithium ion rechargeable batteries such as dimethyl carbonate, diethyl carbonate and the like.

Use

The first publication on vinylene carbonate described its Diels-Alder reaction using the example of its addition reaction with 2,3-dimethylbutadiene to a bicyclic carbonate and subsequent hydrolysis to cis-4,5-dihydroxy-1,2-cyclohexene:[3]

Cis-4,5-Dihydroxy-1,2-cyclohexen-Synthese

When cyclopentadiene is used as the diene, the vicinal norbornene diol bicyclo[2.2.1]hept-5-ene-2,3-diol is formed after hydrolysis. The Swern oxidation to the 1,2-ketone bicyclo[2.2.1]hept-5-ene-2,3-dione proceeds (in the variant with trifluoroacetic anhydride instead of oxalyl chloride) with a yield of 73%.[14]

Norbornendion

Under UV irradiation, ketones react with vinylene carbonate to form bicyclic exo-oxetanes:

VC addition to ketones

With phosphorus(V)sulfide, vinylene carbonate reacts to the corresponding vinylenethionocarbonate (2-thiono-1,3-dioxol-4-ene)[15], which gives ketene in quantitative yield upon UV irradiation. The reaction is a good alternative to the decomposition of α-diazoketones.[16]

Keten aus Vinylencarbonat

Vinylene carbonate is used widely as an electrolyte additive for lithium-ion batteries where it promotes the formation of an insoluble film between the electrolyte and the negative electrode: the SEI (solid-electrolyte-interface).[17] This polymer film allows ionic conduction, but prevents the reduction of the electrolyte at the negative (graphite) electrode and contributes significantly to the long-term stability of lithium-ion batteries.[18][19] A 2013 publication suggests that the cyclic sultone 3-fluoro-1,3-propanesultone (FPS) is superior to vinylene carbonate in SEI formation.[20]

3-Fluor-1,3-propansulton

Since 1,3-propane sultone (on which FPS is based) is classified as a particularly dangerous carcinogenic substance, a significant hazard potential must also be assumed for FPS.

Polymers

Already the first work on vinylene carbonate describes its bulk polymerization a colorless polymer, which is water soluble after hydrolysis.[3] Subsequent publications suggest that the first authors produced only low molecular weight oligomers.[21][22] The preparation of higher molecular weight polymers with useful properties depends critically on the purity of the monomeric vinylene carbonate.[23] Vinylene carbonate can be homopolymerized in bulk, in solution, in suspension and in dispersion using radical initiators such as azobis(isobutyronitrile) (AIBN) or benzoyl peroxide. It can also be copolymerized with other vinyl monomers such as vinyl pyrrolidone or vinyl propionate.[24]

Polymerisation von Vinylencarbonat

Polyvinylene carbonate is readily soluble in acetone and dimethylformamide. The solutions obtained, however, tend to decompose already at room temperature.[25] The patent literature describes the use of polyvinyl carbonate for strong fibers, clear, colorless and mechanically strong films,[21][10] membranes for reverse osmosis[26] and as support during affinity chromatography.[27]

In addition to the instability in solutions, polyvinyl carbonate has the tendency towards hydrolysis in weakly alkaline medium. This forms polyhydroxymethylene (PHM) via cleavage of the cyclic carbon ring, with the repeating unit –(CHOH)–. Its behavior is much more similar to cellulose than to the structurally related polyvinyl alcohol with the repeating unit –(CH2–CHOH)–.

Hydrolyse von Polyvinylencarbonat zu Polyhydroxymethylen

For example, polyhydroxymethylene films obtained by alkaline hydrolysis of polyvinylene carbonate films via sodium methoxide in methanol are crystalline and exhibit high tensile strengths.[10] Analogous to cellulose, polyhydroxymethylene can be dissolved in hot sodium hydroxide solution and converted by crosslinking into a highly swellable polymer which can take up to 10,000 times its weight in water.[28] Polyhydroxymethylene is soluble in anhydrous hydrazine[29] and can be converted into cellulose-like fibers by spinning in water. Similar to cellulose, polyhydroxymethylene reacts with carbon disulfide in the alkaline state to form a xanthate, from which water-insoluble polyhydroxymethylene is again obtained by precipitation in dilute sulfuric acid.[30]

Safety

Vinylene carbonate requires particular care when handling because of its problematic toxicological and ecotoxicological profile[1] and its potential carcinogenic properties.[31]

References

  1. ^ a b Sigma-Aldrich Co., product no. {{{id}}}.
  2. ^ Haynes, W. M., ed. (2016). CRC Handbook of Chemistry and Physics (96th ed.). Boca Raton, Florida: CRC Press/Taylor & Francis. p. 3-228. ISBN 978-1482260960.
  3. ^ a b c M. S. Newman, R. W. Addor (1953), "Vinylene Carbonate", Journal of the American Chemical Society (in German), vol. 75, no. 5, pp. 1263–1264, doi:10.1021/ja01101a526
  4. ^ a b c US 6395908, B. Seifert et al., "Process for the preparation of vinylene carbonate, and the use thereof", issued 2002-05-28, assigned to Merck Patentgesellschaft 
  5. ^ EP 1881972, Reinhard Langer, Anke Beckmann, Paul Wagner, Heinrich Grzinia, Marielouise Schneider, Ulrich Notheis, Lars Rodefeld, Nikolaus Müller, "Process for producing vinylene carbonate", issued 2013-08-28, assigned to Saltigo GmbH 
  6. ^ a b US 8022231, M. Lerm et al., "Process for preparing monochloroethylene carbonate and subsequent conversion to vinylene carbonate", issued 2011-09-20, assigned to Evonik Degussa GmbH 
  7. ^ EP 1881973, R. Langer et al., "PROCESS FOR PRODUCING VINYLENE CARBONATE", issued 2008-01-30 
  8. ^ GB 899205, B.F. Nesbitt, I. Goodman, "The purification and polymerisation of vinylene carbonate", issued 1962-06-20, assigned to ICI Ltd. 
  9. ^ Morris Zief, Hollister Ruch, Charles H. Schramm (1963), "Low temperature zone refining apparatus", Journal of Chemical Education (in German), vol. 40, no. 7, p. 351, doi:10.1021/ed040p351{{citation}}: CS1 maint: multiple names: authors list (link)
  10. ^ a b c N. D. Field, J. R. Schaefgen (1962), "High molecular weight poly(vinylene carbonate) and derivatives", Journal of Polymer Science A: Polymer Chemistry (in German), vol. 58, no. 166, pp. 533–543, doi:10.1002/pol.1962.1205816630
  11. ^ PCT-Anmeldung WO 2006/119910, Verfahren zur Reinigung von Vinylencarbonat, invent1: R. Langer et al., assign1: Lanxess Deutschland GmbH, veröffentlicht am 16. November 2006.
  12. ^ EP 1881971, Reinhard Langer, Paul Wagner, Heinrich Grzinia, "High-purity vinylene carbonate and a method of purifying vinylene carbonate", issued 2008-01-30, assigned to Saltigo GmbH 
  13. ^ WO 2006119908, R. Langer, "METHOD OF STORING AND TRANSPORTING VINYLENE CARBONATE", issued 2006-11-16, assigned to Lanxess Deutschland GmbH 
  14. ^ T. Kobayashi, S. Kobayashi (2000), "Swern Oxidation of Bicyclo[2.2.1]hept-5-ene-2,3-diol and Its Pyrazine-fused Derivatives: An Improved Synthesis of Bicyclo[2.2.1]hept-5-ene-2,3-dione and An Unexpected Ring-Opening Reaction", Molecules (in German), vol. 5, no. 9, pp. 1062–1067, doi:10.3390/50901062{{citation}}: CS1 maint: unflagged free DOI (link)
  15. ^ Hans-Michael Fischler, Willy Hartmann (1972), "Notiz über die Darstellung von Vinylenthioncarbonat und einigen alkyl- sowie arylsubstituierten Derivaten", Chemische Berichte (in German), vol. 105, no. 8, pp. 2769–2771, doi:10.1002/cber.19721050838
  16. ^ Handbook of Reagents for Organic Syntheses, Sulfur-Containing Reagents, ed. L.A. Paquette, Wiley-VCH, 2010, ISBN 978-0-470-74872-5, S. 535.
  17. ^ Hsiang-Hwan Lee, Yung-Yun Wang, Chi-Chao Wan, Mo-Hua Yang, Hung-Chun Wu, Deng-Tswen Shieh (2005), "The function of vinylene carbonate as a thermal additive to electrolyte in lithium batteries", Journal of Applied Electrochemistry (in German), vol. 35, no. 6, pp. 615–623, doi:10.1007/s10800-005-2700-x{{citation}}: CS1 maint: multiple names: authors list (link)
  18. ^ M. Broussely et al., Main aging mechanisms in Li ion batteries, J. Power Sources, 146 (1), 90–96 (2005), doi:10.1016/j.jpowsour.2005.03.172.
  19. ^ DE 102004018929, V. Hennige et al., "Elektrolytzusammensetzung sowie deren Verwendung als Elektrolytmaterial für elektrochemische Energiespeichersysteme", issued 2005-11-17, assigned to assign1 Degussa AG 
  20. ^ H.M. Jung et al., Fluoropropane sultone as an SEI-forming additive that outperforms vinylene carbonate, J. Mater. Chem. A, 1, 11975–11981 (2013), doi:10.1039/C3TA12580G.
  21. ^ a b US 2993030, G.E. Ham, M. Zief, "Process for polymerizing vinylene carbonate", issued 1961-07-16, assigned to J.T. Baker Chemical Co. 
  22. ^ M. Krebs, C. Schneider, Vinylene carbonate – A study of its polymerization and copolymerization behavior, Adv. Chem., 142 (9), 92–98 (1975), doi:10.1021/ba-1975-0142.ch009.
  23. ^ GB 899205, Brenda Frances Nesbitt, Isaac Goodman, "The purification and polymerisation of vinylene carbonate", issued 1962-06-20, assigned to Imperial Chemical Industries Ltd 
  24. ^ US 4098771, H. Huemer, K. Burg, "Process for the preparation of polymers of vinylene carbonate", issued 1978-07-04, assigned to Hoechst AG 
  25. ^ J. Huang et al., Investigations on vinylene carbonate I. Preparation and properties of poly-(vinylene carbonate), Chinese J. Polym. Sci., 8(3), 197–203 (1990).
  26. ^ US 3332894, P.A. Cantor, R.E. Kesting, "Polyvinyl carbonate desalination membrane and a method of producing the same", issued 1967-07-25 
  27. ^ US 4788278, O. Mauz, "Polyvinylene carbonate and polyhydroxymethylene, processes for their preparation and their use", issued 1988-11-29, assigned to Hoechst AG 
  28. ^ US 4061692, A. Holst, M. Kostrzewa, "Process for the manufacture of swellable, absorptive polymers of polyhydroxy methylene", issued 1977-12-06 
  29. ^ US 4076680, M.K. Akkapeddi, H.K. Reimschuessel, "Poly(hydroxymethylene) solutions", issued 1978-02-28 
  30. ^ US 3331800, H. Schübel et al., "Preparation of solutions of polyhydroxymethylene-containing polymers", issued 1967-07-18 
  31. ^ Entry from Vinylene Carbonate from TCI Europe, retrieved on 5 January 2014
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