Ethylene

Not to be confused with Ethylone.
Ethylene
Names
IUPAC name
Ethene
Identifiers
74-85-1 YesY
ChEBI CHEBI:18153 YesY
ChEMBL ChEMBL117822 YesY
ChemSpider 6085 YesY
EC Number 200-815-3
Jmol 3D model Interactive image
KEGG C06547 YesY
PubChem 6325
UNII 91GW059KN7 YesY
Properties
C
2H
4
Molar mass 28.05 g/mol
Appearance colorless gas
Density 1.178 kg/m3 at 15 °C, gas[1]
Melting point −169.2 °C (−272.6 °F; 104.0 K)
Boiling point −103.7 °C (−154.7 °F; 169.5 K)
3.5 mg/100 mL (17 °C); 2.9 mg/L[2]
Solubility in ethanol 4.22 mg/L[2]
Solubility in diethyl ether good[2]
Acidity (pKa) 44
Structure
D2h
zero
Thermochemistry
219.32 J·K−1·mol−1
+52.47 kJ/mol
Hazards
Safety data sheet See: data page
ICSC 0475
F+
R-phrases R12 R67
S-phrases (S2) S9 S16 S33 S46
NFPA 704
Flammability code 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g., propane Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g., phosphorus Special hazards (white): no codeNFPA 704 four-colored diamond
4
2
2
Flash point −136 °C (−213 °F; 137 K)
542.8 °C (1,009.0 °F; 815.9 K)
Related compounds
Related compounds
 Ethane
Acetylene
Supplementary data page
Refractive index (n),
Dielectric constant (εr), etc.
Thermodynamic
data
 Phase behaviour
solid–liquid–gas
UV, IR, NMR, MS
YesY verify (what is YesYN ?)
Infobox references

Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C
2H
4 or H2C=CH2. It is a colorless flammable gas with a faint "sweet and musky" odor when pure.[3] It is the simplest alkene (a hydrocarbon with carbon-carbon double bonds), and the second simplest unsaturated hydrocarbon after acetylene (C
2H
2).

Ethylene is widely used in the chemical industry, and its worldwide production (over 109 million tonnes in 2006) exceeds that of any other organic compound.[4][5] Much of this production goes toward polyethylene, a widely used plastic containing polymer chains of ethylene units in various chain lengths. Ethylene is also an important natural plant hormone, used in agriculture to force the ripening of fruits.[6] Ethylene's hydrate is ethyl alcohol.

Structure and properties

Orbital description of bonding between ethylene and a transition metal.

This hydrocarbon has four hydrogen atoms bound to a pair of carbon atoms that are connected by a double bond. All six atoms that comprise ethylene are coplanar. The H-C-H angle is 117.4°, close to the 120° for ideal sp² hybridized carbon. The molecule is also relatively rigid: rotation about the C-C bond is a high energy process that requires breaking the π-bond.

The π-bond in the ethylene molecule is responsible for its useful reactivity. The double bond is a region of high electron density, thus it is susceptible to attack by electrophiles. Many reactions of ethylene are catalyzed by transition metals, which bind transiently to the ethylene using both the π and π* orbitals.

Being a simple molecule, ethylene is spectroscopically simple. Its UV-vis spectrum is still used as a test of theoretical methods.[7]

Uses

Major industrial reactions of ethylene include in order of scale: 1) polymerization, 2) oxidation, 3) halogenation and hydrohalogenation, 4) alkylation, 5) hydration, 6) oligomerization, and 7) hydroformylation. In the United States and Europe, approximately 90% of ethylene is used to produce ethylene oxide, ethylene dichloride, ethylbenzene and polyethylene.[8] Most of the reactions with ethylene are electrophilic addition.

Main industrial uses of ethylene. Clockwise from the upper right: its conversions to ethylene oxide, precursor to ethylene glycol; to ethylbenzene, precursor to styrene; to various kinds of polyethylene; to ethylene dichloride, precursor to vinyl chloride.

Polymerization

Polyethylene consumes more than half of the world's ethylene supply. Polyethylene, also called polythene, is the world's most widely used plastic. It is primarily used to make films in packaging, carrier bags and trash liners. Linear alpha-olefins, produced by oligomerization (formation of short polymers) are used as precursors, detergents, plasticisers, synthetic lubricants, additives, and also as co-monomers in the production of polyethylenes.[8]

Oxidation

Ethylene is oxidized to produce ethylene oxide, a key raw material in the production of surfactants and detergents by ethoxylation. Ethylene oxide is also hydrolyzed to produce ethylene glycol, widely used as an automotive antifreeze as well as higher molecular weight glycols, glycol ethers and polyethylene terephthalate.

Main article: Wacker process

Ethylene undergoes oxidation by palladium to give acetaldehyde. This conversion remains a major industrial process (10M kg/y).[9] The process proceeds via the initial complexation of ethylene to a Pd(II) center.

Halogenation and hydrohalogenation

Major intermediates from the halogenation and hydrohalogenation of ethylene include ethylene dichloride, ethyl chloride and ethylene dibromide. The addition of chlorine entails "oxychlorination," i.e. chlorine itself is not used. Some products derived from this group are polyvinyl chloride, trichloroethylene, perchloroethylene, methyl chloroform, polyvinylidene chloride and copolymers, and ethyl bromide.[10]

Alkylation

Major chemical intermediates from the alkylation with ethylene is ethylbenzene, precursor to styrene. Styrene is used principally in polystyrene for packaging and insulation, as well as in styrene-butadiene rubber for tires and footwear. On a smaller scale, ethyltoluene, ethylanilines, 1,4-hexadiene, and aluminium alkyls. Products of these intermediates include polystyrene, unsaturated polyesters and ethylene-propylene terpolymers.[10]

Oxo reaction

The hydroformylation (oxo reaction) of ethylene results in propionaldehyde, a precursor to propionic acid and n-propyl alcohol.[10]

Hydration

Ethylene has long represented the major nonfermentative precursor to ethanol. The original method entailed its conversion to diethyl sulfate, followed by hydrolysis. The main method practiced since the mid-1990s is the direct hydration of ethylene catalyzed by solid acid catalysts:[11]

C2H4 + H2O → CH3CH2OH

Dimerization to n-Butenes

Ethylene can be dimerized to n-butenes using processes licensed by Lummus or IFP. The Lummus process produces mixed n-butenes (primarily 2-butenes) while the IFP process produces 1-butene.

Niche uses

An example of a niche use is as an anesthetic agent (in an 85% ethylene/15% oxygen ratio).[12] It can also be used to hasten fruit ripening, as well as a welding gas.[8][13]

Production

Global ethylene production was 107 million tonnes in 2005,[4] 109 million tonnes in 2006,[14] 138 million tonnes in 2010 and 141 million tonnes in 2011.[15] By 2013 ethylene was produced by at least 117 companies in 32 countries. To meet the ever increasing demand for ethylene, sharp increases in production facilities are added globally, particularly in the Mideast and in China.[16]

Industrial Process

Ethylene is produced in the petrochemical industry by steam cracking. In this process, gaseous or light liquid hydrocarbons are heated to 750–950 °C, inducing numerous free radical reactions followed by immediate quench to stop these reactions. This process converts large hydrocarbons into smaller ones and introduces unsaturation. Ethylene is separated from the resulting complex mixture by repeated compression and distillation. In a related process used in oil refineries, high molecular weight hydrocarbons are cracked over zeolite catalysts. Heavier feedstocks, such as naphtha and gas oils require at least two "quench towers" downstream of the cracking furnaces to recirculate pyrolysis-derived gasoline and process water. When cracking a mixture of ethane and propane, only one water quench tower is required.[10]

The areas of an ethylene plant are:

  1. steam cracking furnaces:
  2. primary and secondary heat recovery with quench;
  3. a dilution steam recycle system between the furnaces and the quench system;
  4. primary compression of the cracked gas (3 stages of compression);
  5. hydrogen sulfide and carbon dioxide removal (acid gas removal);
  6. secondary compression (1 or 2 stages);
  7. drying of the cracked gas;
  8. cryogenic treatment;
  9. all of the cold cracked gas stream goes to the demethanizer tower. The overhead stream from the demethanizer tower consists of all the hydrogen and methane that was in the cracked gas stream. Cryogenically (−250 °F (−157 °C)) treating this overhead stream separates hydrogen from methane. Methane recovery is critical to the economical operation of an ethylene plant.
  10. the bottom stream from the demethanizer tower goes to the deethanizer tower. The overhead stream from the deethanizer tower consists of all the C
    2    's that were in the cracked gas stream. The C
    2     stream contains acetylene, which is explosive above 200 kPa (29 psi).[17] If the partial pressure of acetylene is expected to exceed these values, the C
    2     stream is partially hydrogenated. The C
    2    's then proceed to a C
    2     splitter. The product ethylene is taken from the overhead of the tower and the ethane coming from the bottom of the splitter is recycled to the furnaces to be cracked again;
  11. the bottom stream from the de-ethanizer tower goes to the depropanizer tower. The overhead stream from the depropanizer tower consists of all the C
    3    's that were in the cracked gas stream. Before feeding the C
    3    's to the C
    3     splitter, the stream is hydrogenated to convert the methylacetylene and propadiene (allene) mix. This stream is then sent to the C
    3     splitter. The overhead stream from the C
    3     splitter is product propylene and the bottom stream is propane which is sent back to the furnaces for cracking or used as fuel.
  12. The bottom stream from the depropanizer tower is fed to the debutanizer tower. The overhead stream from the debutanizer is all of the C
    4    's that were in the cracked gas stream. The bottom stream from the debutanizer (light pyrolysis gasoline) consists of everything in the cracked gas stream that is C
    5     or heavier.[10]

Since ethylene production is energy intensive, much effort has been dedicated to recovering heat from the gas leaving the furnaces. Most of the energy recovered from the cracked gas is used to make high pressure (1200 psig) steam. This steam is in turn used to drive the turbines for compressing cracked gas, the propylene refrigeration compressor, and the ethylene refrigeration compressor. An ethylene plant, once running, does not need to import steam to drive its steam turbines. A typical world scale ethylene plant (about 1.5 billion pounds of ethylene per year) uses a 45,000 horsepower (34,000 kW) cracked gas compressor, a 30,000 hp (22,000 kW) propylene compressor, and a 15,000 hp (11,000 kW) ethylene compressor.

Laboratory synthesis

Although of great value industrially, ethylene is rarely used in the laboratory and is ordinarily purchased.[18] It can be produced via dehydration of ethanol with sulfuric acid or in the gas phase with aluminium oxide.[19]

Ethylene as a plant hormone

An ethylene signal transduction pathway. Ethylene permeates the membrane and binds to a receptor on the endoplasmic reticulum. The receptor releases the repressed EIN2. This then activates a signal transduction pathway which activates a regulatory genes that eventually trigger an Ethylene response. The activated DNA is transcribed into mRNA which is then translated into a functional enzyme that is used for ethylene biosynthesis.

Ethylene serves as a hormone in plants.[20] It acts at trace levels throughout the life of the plant by stimulating or regulating the ripening of fruit, the opening of flowers, and the abscission (or shedding) of leaves. Commercial ripening rooms use "catalytic generators" to make ethylene gas from a liquid supply of ethanol. Typically, a gassing level of 500 to 2,000 ppm is used, for 24 to 48 hours. Care must be taken to control carbon dioxide levels in ripening rooms when gassing, as high temperature ripening (20 °C; 68 °F) has been seen to produce CO2 levels of 10% in 24 hours.[21]

History of ethylene in plant biology

Ethylene has been used since the ancient Egyptians, who would gash figs in order to stimulate ripening (wounding stimulates ethylene production by plant tissues). The ancient Chinese would burn incense in closed rooms to enhance the ripening of pears. In 1864, it was discovered that gas leaks from street lights led to stunting of growth, twisting of plants, and abnormal thickening of stems.[20] In 1901, a Russian scientist named Dimitry Neljubow showed that the active component was ethylene.[22] Sarah Doubt discovered that ethylene stimulated abscission in 1917.[23] It was not until 1934 that Gane reported that plants synthesize ethylene.[24] In 1935, Crocker proposed that ethylene was the plant hormone responsible for fruit ripening as well as senescence of vegetative tissues.[25]

Ethylene biosynthesis in plants

The Yang cycle

Ethylene is produced from essentially all parts of higher plants, including leaves, stems, roots, flowers, fruits, tubers, and seeds. Ethylene production is regulated by a variety of developmental and environmental factors. During the life of the plant, ethylene production is induced during certain stages of growth such as germination, ripening of fruits, abscission of leaves, and senescence of flowers. Ethylene production can also be induced by a variety of external aspects such as mechanical wounding, environmental stresses, and certain chemicals including auxin and other regulators.[26] The pathway for ethylene biosynthesis is named the Yang cycle after the scientist Shang Fa Yang who made key contributions to elucidating this pathway.

Ethylene is biosynthesized from the amino acid methionine to S-adenosyl-L-methionine (SAM, also called Adomet) by the enzyme Met Adenosyltransferase. SAM is then converted to 1-aminocyclopropane-1-carboxylic acid (ACC) by the enzyme ACC synthase (ACS). The activity of ACS determines the rate of ethylene production, therefore regulation of this enzyme is key for the ethylene biosynthesis. The final step requires oxygen and involves the action of the enzyme ACC-oxidase (ACO), formerly known as the ethylene forming enzyme (EFE). Ethylene biosynthesis can be induced by endogenous or exogenous ethylene. ACC synthesis increases with high levels of auxins, especially indole acetic acid (IAA) and cytokinins.

Ethylene perception in plants

Ethylene is perceived by a family of five transmembrane protein dimers such as the ETR1 protein in Arabidopsis. The genes encoding ethylene receptors have been cloned in the reference plant Arabidopsis thaliana and many other plants. Ethylene receptors are encoded by multiple genes in plant genomes. Dominant missense mutations in any of the gene family, which comprises five receptors in Arabidopsis and at least six in tomato, can confer insensitivity to ethylene.[27] Loss-of-function mutations in multiple members of the ethylene-receptor family result in a plant that exhibits constitutive ethylene responses.[28] DNA sequences for ethylene receptors have also been identified in many other plant species and an ethylene binding protein has even been identified in Cyanobacteria.[20]

Environmental and biological triggers of ethylene

Environmental cues such as flooding, drought, chilling, wounding, and pathogen attack can induce ethylene formation in plants. In flooding, roots suffer from lack of oxygen, or anoxia, which leads to the synthesis of 1-aminocyclopropane-1-carboxylic acid (ACC). ACC is transported upwards in the plant and then oxidized in leaves. The ethylene produced causes nastic movements (epinasty) of the leaves, perhaps helping the plant to lose water.[29]

List of plant responses to ethylene

Commercial issues

Ethylene shortens the shelf life of many fruits by hastening fruit ripening and floral senescence. Ethylene will shorten the shelf life of cut flowers and potted plants by accelerating floral senescence and floral abscission. Flowers and plants which are subjected to stress during shipping, handling, or storage produce ethylene causing a significant reduction in floral display. Flowers affected by ethylene include carnation, geranium, petunia, rose, and many others.[32]

Ethylene can cause significant economic losses for florists, markets, suppliers, and growers. Researchers have developed several ways to inhibit ethylene, including inhibiting ethylene synthesis and inhibiting ethylene perception. Aminoethoxyvinylglycine (AVG), Aminooxyacetic acid (AOA), and silver salts are ethylene inhibitors.[33][34] Inhibiting ethylene synthesis is less effective for reducing post-harvest losses since ethylene from other sources can still have an effect. By inhibiting ethylene perception, fruits, plants and flowers don't respond to ethylene produced endogenously or from exogenous sources. Inhibitors of ethylene perception include compounds that have a similar shape to ethylene, but do not elicit the ethylene response. One example of an ethylene perception inhibitor is 1-methylcyclopropene (1-MCP).

Commercial growers of bromeliads, including pineapple plants, use ethylene to induce flowering. Plants can be induced to flower either by treatment with the gas in a chamber, or by placing a banana peel next to the plant in an enclosed area.

Chrysanthemum flowering is delayed by ethylene gas[35] and growers have found that carbon dioxide 'burners' and the exhaust fumes from inefficient glasshouse heaters can raise the ethylene concentration to 0.05 ppmv causing delay in flowering of commercial crops.

Ligand

Ethylene is a ligand in organometallic chemistry. One of the first organometallic compounds, Zeise's salt is a complex of ethylene. Useful reagents containing ethylene include Pt(PPh3)2(C2H4) and Rh2Cl2(C2H4)4. The Rh-catalysed hydroformylation of ethylene is conducted on industrial scale to provide propionaldehyde.

History

Some geologists and scholars believe that the famous Greek Oracle at Delphi (the Pythia) went into her trance-like state as an effect of ethylene rising from ground faults.[36]

Ethylene appears to have been discovered by Johann Joachim Becher, who obtained it by heating ethanol with sulfuric acid;[37] he mentioned the gas in his Physica Subterranea (1669).[38] Joseph Priestley also mentions the gas in his Experiments and observations relating to the various branches of natural philosophy: with a continuation of the observations on air (1779), where he reports that Jan Ingenhousz saw ethylene synthesized in the same way by a Mr. Enée in Amsterdam in 1777 and that Ingenhousz subsequently produced the gas himself.[39] The properties of ethylene were studied in 1795 by four Dutch chemists, Johann Rudolph Deimann, Adrien Paets van Troostwyck, Anthoni Lauwerenburgh and Nicolas Bondt, who found that it differed from hydrogen gas and that it contained both carbon and hydrogen.[40] This group also discovered that ethylene could be combined with chlorine to produce the oil of the Dutch chemists, 1,2-dichloroethane; this discovery gave ethylene the name used for it at that time, olefiant gas (oil-making gas.)[41]

In the mid-19th century, the suffix -ene (an Ancient Greek root added to the end of female names meaning "daughter of") was widely used to refer to a molecule or part thereof that contained one fewer hydrogen atoms than the molecule being modified. Thus, ethylene (C
2H
4) was the "daughter of ethyl" (C
2H
5). The name ethylene was used in this sense as early as 1852.

In 1866, the German chemist August Wilhelm von Hofmann proposed a system of hydrocarbon nomenclature in which the suffixes -ane, -ene, -ine, -one, and -une were used to denote the hydrocarbons with 0, 2, 4, 6, and 8 fewer hydrogens than their parent alkane.[42] In this system, ethylene became ethene. Hofmann's system eventually became the basis for the Geneva nomenclature approved by the International Congress of Chemists in 1892, which remains at the core of the IUPAC nomenclature. However, by that time, the name ethylene was deeply entrenched, and it remains in wide use today, especially in the chemical industry.

Following experimentation by Luckhardt, Crocker, and Carter at the University of Chicago,[43] ethylene was used as an anesthetic[44][45] It remained in use through the 1940s use even while chloroform was being phased out. Its pungent odor and its explosive nature limit its use today.

Nomenclature

The 1979 IUPAC nomenclature rules made an exception for retaining the non-systematic name ethylene,[46] however, this decision was reversed in the 1993 rules[47] so the IUPAC name is now ethene.

Safety

Like all hydrocarbons, ethylene is an asphyxiant and combustible. It is listed as an IARC class 3 carcinogen.

References

  1. ↑ Record of Ethylene in the GESTIS Substance Database of the IFA, accessed on 25 October 2007
  2. 1 2 3 Neiland, O. Ya. (1990) Органическая химия: Учебник для хим. спец. вузов. Moscow. Vysshaya Shkola. p. 128.
  3. ↑ Booth, H. S. and Campbell, M. B. (1926) Studies of Anesthetic Ethylene: I. The Odor of Ethylene. Anesthesia and Analgesia, July–August 1929, pages 221–226.
  4. 1 2 "Production: Growth is the Norm". Chemical and Engineering News (PDF) 84 (28): 59–236. July 10, 2006. doi:10.1021/cen-v084n034.p059.
  5. ↑ "Propylene Production from Methanol". by Intratec, ISBN 978-0-615-64811-8.
  6. ↑ Wang K, Li H, Ecker J; Li; Ecker (2002). "Ethylene Biosynthesis and Signaling Networks". Plant Cell 14 (Suppl): S131–51. doi:10.1105/tpc.001768 (inactive 2016-05-06). PMC 151252. PMID 12045274.
  7. ↑ "Ethylene:UV/Visible Spectrum". NIST Webbook. Retrieved 2006-09-27.
  8. 1 2 3 "OECD SIDS Initial Assessment Profile — Ethylene" (PDF). inchem.org. Retrieved 2008-05-21.
  9. ↑ Elschenbroich, C.; Salzer, A. (2006). Organometallics : A Concise Introduction (2nd ed.). Weinheim: Wiley-VCH. ISBN 3-527-28165-7.
  10. 1 2 3 4 5 Kniel, Ludwig; Winter, Olaf; Stork, Karl (1980). Ethylene, keystone to the petrochemical industry. New York: M. Dekker. ISBN 0-8247-6914-7.
  11. ↑ Naim Kosaric, Zdravko Duvnjak, Adalbert Farkas, Hermann Sahm, Stephanie Bringer-Meyer, Otto Goebel and Dieter Mayer in "Ethanol" Ullmann's Encyclopedia of Industrial Chemistry, 2011, Wiley-VCH, Weinheim. doi:10.1002/14356007.a09_587.pub2
  12. ↑ Trout, Hugh H. (1927). "Blood Changes Under Ethylene Anæsthesia". Annals of Surgery 86 (2): 260–7. doi:10.1097/00000658-192708000-00013. PMC 1399426. PMID 17865725.
  13. ↑ "Informational Bulletin" 12. California Fresh Market Advisory Board. June 1, 1976.
  14. ↑ Nattrass, L and Higson, A (22 July 2010) NNFCC Renewable Chemicals Factsheet: Ethanol. National Non-Food Crops Centre
  15. ↑ True, Warren R. (2012). "Global ethylene capacity poised for major expansion" 110 (7): 90–95.
  16. ↑ "Market Study: Ethylene (2nd edition), Ceresana, November 2014". ceresana.com. Retrieved 2015-02-03.
  17. ↑ Korzun, Mikołaj (1986). 1000 słów o materiałach wybuchowych i wybuchu. Warszawa: Wydawnictwo Ministerstwa Obrony Narodowej. ISBN 83-11-07044-X. OCLC 69535236.
  18. ↑ Crimmins, M.T.; Kim-Meade, A.S. (2004). "Ethylene". In Paquette, L. Encyclopedia of Reagents for Organic Synthesis. New York: Wiley. doi:10.1002/047084289.
  19. ↑ Cohen, Julius B. (1930). Practical Organic Chemistry (preparation 4). Macmillan.
  20. 1 2 3 Lin, Z.; Zhong, S.; Grierson, D. (2009). "Recent advances in ethylene research". J. Exp. Bot. 60 (12): 3311–36. doi:10.1093/jxb/erp204. PMID 19567479.
  21. ↑ External Link to More on Ethylene Gassing and Carbon Dioxide Control. ne-postharvest.com
  22. ↑ Neljubov D. (1901). "Uber die horizontale Nutation der Stengel von Pisum sativum und einiger anderen Pflanzen". Beih Bot Zentralbl 10: 128–139.
  23. ↑ Doubt, Sarah L. (1917). "The Response of Plants to Illuminating Gas". Botanical Gazette 63 (3): 209–224. doi:10.1086/332006. JSTOR 2469142.
  24. ↑ Gane, R. (1934). "Production of ethylene by some fruits". Nature 134 (3400): 1008. Bibcode:1934Natur.134.1008G. doi:10.1038/1341008a0.
  25. ↑ Crocker W, Hitchcock AE, Zimmerman PW. (1935) "Similarities in the effects of ethlyene and the plant auxins". Contrib. Boyce Thompson Inst. 7. 231-48. Auxins Cytokinins IAA Growth substances, Ethylene
  26. ↑ Yang, S. F. and Hoffman N. E. (1984). "Ethylene biosynthesis and its regulation in higher plants". Annu. Rev. Plant Physiol. 35: 155–89. doi:10.1146/annurev.pp.35.060184.001103.
  27. ↑ Bleecker, A. B.; Esch, J. J.; Hall, A. E.; Rodríguez, F. I.; Binder, B. M. (1998). "The ethylene-receptor family from Arabidopsis: Structure and function". Philosophical Transactions of the Royal Society B: Biological Sciences 353 (1374): 1405–12. doi:10.1098/rstb.1998.0295. PMC 1692356. PMID 9800203.
  28. ↑ Hua, Jian; Meyerowitz, Elliot (1998). "Ethylene responses are negatively regulated by a receptor gene family in Arabidopsis thaliana". Cell 94 (2): 261–271. doi:10.1016/S0092-8674(00)81425-7. PMID 9695954.
  29. ↑ Explaining Epinasty. planthormones.inf
  30. ↑ Wilmowicz E, Kesy J, Kopcewicz J; Kesy; Kopcewicz (December 2008). "Ethylene and ABA interactions in the regulation of flower induction in Pharbitis nil". J. Plant Physiol. 165 (18): 1917–28. doi:10.1016/j.jplph.2008.04.009. PMID 18565620.
  31. ↑ Cockshull KE, Horridge JS (1978). "2-Chloroethylphosphonic Acid and Flower Initiation by Chrysanthemum morifolium Ramat. In Short Days and in Long Days". Journal of Horticultural Science & Biotechnology 53 (2): 85–90.
  32. ↑ Van Doorn, W. G. (2002). "Effect of ethylene on flower abscission: a survey". Annals of Botany 89 (6): 689–693. doi:10.1093/aob/mcf124. PMC 4233834. PMID 12102524.
  33. ↑ Cassells, A. C.; Peter B. Gahan (2006). Dictionary of plant tissue culture. Haworth Press. p. 77. ISBN 978-1-56022-919-3.
  34. ↑ Constabel, Friedrich; Jerry P. Shyluk (1994). "1: Initiation, Nutrition, and Maintenance of Plant Cell and Tissue Cultures". Plant Cell and Tissue Culture. Springer. p. 5. ISBN 0-7923-2493-5.
  35. ↑ van Berkel, N. (1987). "Injurious effects of low ethylene concentrations on Chrysanthemum morifolium Ramat". Acta Hort. (ISHS) 197: 43–52.
  36. ↑ John Roach (2001-08-14). "Delphic Oracle's Lips May Have Been Loosened by Gas Vapors". National Geographic. Retrieved March 8, 2007.
  37. ↑ Roscoe, Henry Enfield; Schorlemmer, Carl (1878). A treatise on chemistry 1. D. Appleton. p. 611.
  38. ↑ Brown, James Campbell (July 2006). A History of Chemistry: From the Earliest Times Till the Present Day. Kessinger. p. 225. ISBN 978-1-4286-3831-0.
  39. ↑ Appendix, §VIII, pp. 474 ff., Experiments and observations relating to the various branches of natural philosophy: with a continuation of the observations on air, Joseph Priestley, London: printed for J. Johnson, 1779, vol. 1.
  40. ↑ Roscoe & Schorlemmer 1878, p. 612
  41. ↑ Roscoe & Schorlemmer 1878, p. 613
    Gregory, William (1857). Handbook of organic chemistry (4th American ed.). A.S. Barnes & Co. p. 157.
  42. ↑ Hofmann, A. W. "Hofmann's Proposal for Systematic Nomenclature of the Hydrocarbons". www.chem.yale.edu. Retrieved 2007-01-06.
  43. ↑ Luckhardt, Arno; Carter, J. B. (1 Dec 1923). "Ethylene as a gas anesthetic". Current Researches in Anesthesisa & Analgeisa 2 (6): 221–229. Retrieved 11 January 2015.
  44. ↑ Johnstone, George A. Johnstone (1 Aug 1927). "Advantages of Ethylene-Oxygen as an anesthetic". California and Western Medicine (ACS) 27 (2): 216–218. PMC 1655579. PMID 18740435.
  45. ↑ Zimmermann, Heinz; Walz, Roland (2008). "Ethylene". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_045.pub3.
  46. ↑ IUPAC nomenclature rule A-3.1 (1979). Acdlabs.com. Retrieved on 2016-04-24.
  47. ↑ Footnote to IUPAC nomenclature rule R-9.1, table 19(b). Acdlabs.com. Retrieved on 2016-04-24.

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