Organofluorine chemistry

Organofluorine chemistry describes the chemistry of organofluorine compounds, organic compounds that contain a carbon–fluorine bond. Organofluorine compounds find diverse applications ranging from oil and water repellents to pharmaceuticals, refrigerants, and reagents in catalysis. In addition to these applications, some organofluorine compounds are pollutants because of their contributions to ozone depletion, global warming, bioaccumulation, and toxicity. The area of organofluorine chemistry often requires special techniques associated with the handling of fluorinating agents.

The carbon–fluorine bond
Main article: Carbon-fluorine bond

Fluorine has several distinctive differences from all other substituents encountered in organic molecules. As a result, the physical and chemical properties of organofluorines can be distinctive in comparison to other organohalogens.

  1. The carbon–fluorine bond is one of the strongest in organic chemistry (an average bond energy around 480 kJ/mol[1]). This is significantly stronger than the bonds of carbon with other halogens (an average bond energy of e.g. C-Cl bond is around 320 kJ/mol[1]) and is one of the reasons why fluoroorganic compounds have high thermal and chemical stability.
  2. The carbon–fluorine bond is relatively short (around 1.4 Å[1]).
  3. The Van der Waals radius of the fluorine substituent is only 1.47 Å,[1] which is shorter than in any other substituent and is close to that of hydrogen (1.2 Å). This, together with the short bond length, is the reason why there is no steric strain in polyfluorinated compounds. This is another reason for their high thermal stability. In addition, the fluorine substituents in polyfluorinated compounds efficiently shield the carbon skeleton from possible attacking reagents. This is another reason for the high chemical stability of polyfluorinated compounds.
  4. Fluorine has the highest electronegativity of all elements: 3.98.[1] This causes the high dipole moment of C-F bond (1.41 D[1]).
  5. Fluorine has the lowest polarizability of all atoms: 0.56 10−24 cm3.[1] This causes very weak dispersion forces between polyfluorinated molecules and is the reason for the often-observed boiling point reduction on fluorination as well as for the simultaneous hydrophobicity and lipophobicity of polyfluorinated compounds whereas other perhalogenated compounds are more lipophilic.

In comparison to aryl chlorides and bromides, aryl fluorides form Grignard reagents only reluctantly. On the other hand, aryl fluorides, e.g. fluoroanilines and fluorophenols, often undergo nucleophilic substitution efficiently.[2]

Types of organofluorine compounds

Fluorocarbons
Main article: Perfluorocarbon

Formally, fluorocarbons only contain carbon and fluorine. Sometimes they are called perfluorocarbons. They can be gases, liquids, waxes, or solids, depending upon their molecular weight. The simplest fluorocarbon is the gas tetrafluoromethane (CF4). Liquids include perfluorooctane and perfluorodecalin. While fluorocarbons with single bonds are stable, unsaturated fluorocarbons are more reactive, especially those with triple bonds. Fluorocarbons are more chemically and thermally stable than hydrocarbons, reflecting the relative inertness of the C-F bond. They are also relatively lipophobic. Because of the reduced intermolecular van der Waals interactions, fluorocarbon-based compounds are sometimes used as lubricants or are highly volatile. Fluorocarbon liquids have medical applications as oxygen carriers.

The structure of organofluorine compounds can be distinctive. As shown below, perfluorinated aliphatic compounds tend to segregate from hydrocarbons. This "like dissolves like effect" is related to the usefulness of fluorous phases and the use of PFOA in processing of fluoropolymers. In contrast to the aliphatic derivatives, perfluoroaromatic derivatives tend to form mixed phases with nonfluorinated aromatic compounds, resulting from donor-acceptor interactions between the pi-systems.

Fluoropolymers

Polymeric organofluorine compounds are numerous and commercially significant. They range from fully fluorinated species, e.g. PTFE to partially fluorinated, e.g. polyvinylidene fluoride ([CH2CF2]n) and polychlorotrifluoroethylene ([CFClCF2]n). The fluoropolymer polytetrafluoroethylene (PTFE/Teflon) is a solid.

Hydrofluorocarbons
Main article: Hydrofluorocarbon

Hydrofluorocarbons (HFCs), organic compounds that contain fluorine and hydrogen atoms, are the most common type of organofluorine compounds. They are commonly used in air conditioning and as refrigerants[5] in place of the older chlorofluorocarbons such as R-12 and hydrochlorofluorocarbons such as R-21. They do not harm the ozone layer as much as the compounds they replace; however, they do contribute to global warming. Their atmospheric concentrations and contribution to anthropogenic greenhouse gas emissions are rapidly increasing, causing international concern about their radiative forcing.

Fluorocarbons with few C-F bonds behave similarly to the parent hydrocarbons, but their reactivity can be altered significantly. For example, both uracil and 5-fluorouracil are colourless, high-melting crystalline solids, but the latter is a potent anti-cancer drug. The use of the C-F bond in pharmaceuticals is predicated on this altered reactivity.[6] Several drugs and agrochemicals contain only one fluorine center or one trifluoromethyl group.

Unlike other greenhouse gases in the Paris Agreement, hydrofluorocarbons have other international negotiations.[7]

In September 2016, the so-called New York Declaration urged a global reduction in the use of HFCs.[8] On 15 October 2016, due to these chemicals contribution to climate change, negotiators from 197 nations meeting at the summit of the United Nations Environment Programme in Kigali, Rwanda reached a legally-binding accord to phase out hydrofluorocarbons (HFCs) in an amendment to the Montreal Protocol.[9][10][11]

Fluorocarbenes

As indicated throughout this article, fluorine-substituents lead to reactivity that differs strongly from classical organic chemistry. The premier example is difluorocarbene, CF2, which is a singlet whereas carbene (CH2) has a triplet ground state.[12] This difference is significant because difluorocarbene is a precursor to tetrafluoroethylene.

Perfluorinated compounds
Main article: Perfluorinated compounds

Perfluorinated compounds are fluorocarbon derivatives, as they are closely structurally related to fluorocarbons. However, they also possess new atoms such as nitrogen, iodine, or ionic groups, such as perfluorinated carboxylic acids.

Methods for preparation of C–F bonds

Organofluorine compounds are prepared by numerous routes, depending on the degree and regiochemistry of fluorination sought and the nature of the precursors. The direct fluorination of hydrocarbons with F2, often diluted with N2, is useful for highly fluorinated compounds:

R
3CH + F
2 → R
3CF + HF

Such reactions however are often unselective and require care because hydrocarbons can uncontrollably "burn" in F
2, analogous to the combustion of hydrocarbon in O
2. For this reason, alternative fluorination methodologies have been developed. Generally, such methods are classified into two classes.

Electrophilic fluorination
See also: electrophilic fluorination

Electrophilic fluorination rely on sources of "F+". Often such reagents feature N-F bonds, for example F-TEDA-BF4. Asymmetric fluorination, whereby only one of two possible enantiomeric products are generated from a prochiral substrate, rely on electrophilic fluorination reagents.[13] Illustrative of this approach is the preparation of a precursor to anti-inflammatory agents:[14]

Electrosynthetic methods
Main article: Electrofluorination

A specialized but important method of electrophilic fluorination involves electrosynthesis. The method is mainly used to perfluorinate, i.e. replace all C–H bonds by C–F bonds. The hydrocarbon is dissolved or suspended in liquid HF, and the mixture is electrolyzed at 5–6 V using Ni anodes.[15] The method was first demonstrated with the preparation of perfluoropyridine (C
5F
5N) from pyridine (C
5H
5N). Several variations of this technique have been described, including the use of molten potassium bifluoride or organic solvents.

Nucleophilic fluorination

The major alternative to electrophilic fluorination is nucleophilic fluorination using reagents that are sources of "F−," for Nucleophilic displacement typically of chloride and bromide. Metathesis reactions employing alkali metal fluorides are the simplest.[16] For aliphatic compounds this is sometimes called the Finkelstein reaction, while for aromatic compounds it is known as the Halex process.

R
3CCl + MF → R
3CF + MCl (M = Na, K, Cs)

Alkyl monofluorides can be obtained from alcohols and Olah reagent (pyridinium fluoride) or another fluoridating agents.

The decomposition of aryldiazonium tetrafluoroborates in the Sandmeyer[17] or Schiemann reactions exploit fluoroborates as F− sources.

ArN
2BF
4 → ArF + N
2 + BF
3

Although hydrogen fluoride may appear to be an unlikely nucleophile, it is the most common source of fluoride in the synthesis of organofluorine compounds. Such reactions are often catalysed by metal fluorides such as chromium trifluoride. 1,1,1,2-Tetrafluoroethane, a replacement for CFC's, is prepared industrially using this approach:[18]

Cl2C=CClH + 4 HF → F3CCFH2 + 3 HCl

Notice that this transformation entails two reaction types, metathesis (replacement of Cl− by F−) and hydrofluorination of an alkene.

Deoxofluorination

Deoxofluorination convert a variety of oxygen-containing groups into fluorides. The usual reagent is sulfur tetrafluoride:

RCO2H + SF4 → RCF3 + SO2 + HF

A more convenient alternative to SF4 is the diethylaminosulfur trifluoride, which is a liquid whereas SF4 is a corrosive gas:[19][20]

C6H5CHO + R2NSF3 → C6H5CHF2 + "R2NSOF"

Apart from DAST, a wide variety of similar reagents exist, including, but not limited to, 2-pyridinesulfonyl fluoride (PyFluor) and N-tosyl-4-chlorobenzenesulfonimidoyl fluoride (SulfoxFluor).[21] Many of these display improved properties such as better safety profile, higher thermodynamic stability, ease of handling, high enantioselectivity, and selectivity over elimination side-reactions.[22][23]

From fluorinated building blocks

Many organofluorine compounds are generated from reagents that deliver perfluoroalkyl and perfluoroaryl groups. (Trifluoromethyl)trimethylsilane, CF3Si(CH3)3, is used as a source of the trifluoromethyl group, for example.[24] Among the available fluorinated building blocks are CF3X (X = Br, I), C6F5Br, and C3F7I. These species form Grignard reagents that then can be treated with a variety of electrophiles. The development of fluorous technologies (see below, under solvents) is leading to the development of reagents for the introduction of "fluorous tails".

A special but significant application of the fluorinated building block approach is the synthesis of tetrafluoroethylene, which is produced on a large-scale industrially via the intermediacy of difluorocarbene. The process begins with the thermal (600-800 °C) dehydrochlorination of chlorodifluoromethane:[6]

CHClF2 → CF2 + HCl
2 CF2 → C2F4

Sodium fluorodichloroacetate (CAS# 2837-90-3) is used to generate chlorofluorocarbene, for cyclopropanations.

18F-Delivery methods

The usefulness of fluorine-containing radiopharmaceuticals in 18F-positron emission tomography has motivated the development of new methods for forming C–F bonds. Because of the short half-life of 18F, these syntheses must be highly efficient, rapid, and easy.[25] Illustrative of the methods is the preparation of fluoride-modified glucose by displacement of a triflate by a labeled fluoride nucleophile:

Biological role

Biologically synthesized organofluorines have been found in microorganisms and plants, but not animals.[26] The most common example is fluoroacetate, which occurs as a plant defence against herbivores in at least 40 plants in Australia, Brazil and Africa.[27] Other biologically synthesized organofluorines include ω-fluoro fatty acids, fluoroacetone, and 2-fluorocitrate which are all believed to be biosynthesized in biochemical pathways from the intermediate fluoroacetaldehyde.[26] Adenosyl-fluoride synthase is an enzyme capable of biologically synthesizing the carbon–fluorine bond.[28] Man made carbon–fluorine bonds are commonly found in pharmaceuticals and agrichemicals because it adds stability to the carbon framework; also, the relatively small size of fluorine is convenient as fluorine acts as an approximate bioisostere of the hydrogen. Introducing the carbon–fluorine bond to organic compounds is the major challenge for medicinal chemists using organofluorine chemistry, as the carbon–fluorine bond increases the probability of having a successful drug by about a factor of ten.[29] An estimated 20% of pharmaceuticals, and 30–40% of agrichemicals are organofluorines, including several of the top drugs.[29] Examples include 5-fluorouracil, fluoxetine (Prozac), paroxetine (Paxil), ciprofloxacin (Cipro), mefloquine, and fluconazole.

Applications

Organofluorine chemistry impacts many areas of everyday life and technology. The C-F bond is found in pharmaceuticals, agrichemicals, fluoropolymers, refrigerants, surfactants, anesthetics, oil-repellents, catalysis, and water-repellents, among others.

Pharmaceuticals and agrochemicals

The carbon-fluorine bond is commonly found in pharmaceuticals and agrochemicals because it is generally metabolically stable and fluorine acts as a bioisostere of the hydrogen atom. An estimated 1/5 of pharmaceuticals contain fluorine, including several of the top drugs.[30] Examples include 5-fluorouracil, flunitrazepam (Rohypnol), fluoxetine (Prozac), paroxetine (Paxil), ciprofloxacin (Cipro), mefloquine, and fluconazole. Fluorine-substituted ethers are volatile anesthetics, including the commercial products methoxyflurane, enflurane, isoflurane, sevoflurane and desflurane. Fluorocarbon anesthetics reduce the hazard of flammability with diethyl ether and cyclopropane. Perfluorinated alkanes are used as blood substitutes.

Inhaler propellant

Fluorocarbons are also used as a propellant for metered-dose inhalers used to administer some asthma medications. The current generation of propellant consists of hydrofluoroalkanes (HFA), which have replaced CFC-propellant-based inhalers. CFC inhalers were banned as of 2008 as part of the Montreal Protocol[31] because of environmental concerns with the ozone layer. HFA propellant inhalers like FloVent and ProAir ( Salbutamol ) have no generic versions available as of October 2014.

Fluorosurfactants

Fluorosurfactants, which have a polyfluorinated "tail" and a hydrophilic "head", serve as surfactants because they concentrate at the liquid-air interface due to their lipophobicity. Fluorosurfactants have low surface energies and dramatically lower surface tension. The fluorosurfactants perfluorooctanesulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) are two of the most studied because of their ubiquity, toxicity, and long residence times in humans and wildlife.

Solvents

Fluorinated compounds often display distinct solubility properties. Dichlorodifluoromethane and chlorodifluoromethane were at one time widely used refrigerants. CFCs have potent ozone depletion potential due to the homolytic cleavage of the carbon-chlorine bonds; their use is largely prohibited by the Montreal Protocol. Hydrofluorocarbons (HFCs), such as tetrafluoroethane, serve as CFC replacements because they do not catalyze ozone depletion. Oxygen exhibits a high solubility in perfluorocarbon compounds, reflecting on their lipophilicity. Perfluorodecalin has been demonstrated as a blood substitute transporting oxygen to the lungs.

The solvent 1,1,1,2-tetrafluoroethane has been used for extraction of natural products such as taxol, evening primrose oil, and vanillin. 2,2,2-trifluoroethanol is an oxidation-resistant polar solvent.[32]

Organofluorine reagents

The development of organofluorine chemistry has contributed many reagents of value beyond organofluorine chemistry. Triflic acid (CF3SO3H) and trifluoroacetic acid (CF3CO2H) are useful throughout organic synthesis. Their strong acidity is attributed to the electronegativity of the trifluoromethyl group that stabilizes the negative charge. The triflate-group (the conjugate base of the triflic acid) is a good leaving group in substitution reactions.

Fluorous phases

Of topical interest in the area of "Green Chemistry,"[33] highly fluorinated substituents, e.g. perfluorohexyl (C6F13) confer distinctive solubility properties to molecules, which facilitates purification of products in organic synthesis.[34] This area, described as "fluorous chemistry," exploits the concept of like-dissolves-like in the sense that fluorine-rich compounds dissolve preferentially in fluorine-rich solvents. Because of the relative inertness of the C-F bond, such fluorous phases are compatible with even harsh reagents. This theme has spawned techniques of "fluorous tagging and fluorous protection. Illustrative of fluorous technology is the use of fluoroalkyl-substituted tin hydrides for reductions, the products being easily separated from the spent tin reagent by extraction using fluorinated solvents.[35]

Hydrophobic fluorinated ionic liquids, such as organic salts of bistriflimide or hexafluorophosphate, can form phases that are insoluble in both water and organic solvents, producing multiphasic liquids.

Organofluorine ligands in transition metal chemistry

Organofluorine ligands have long been featured in organometallic and coordination chemistry. One advantage to F-containing ligands is the convenience of 19F NMR spectroscopy for monitoring reactions. The organofluorine compounds can serve as a "sigma-donor ligand," as illustrated by the titanium(III) derivative [(C5Me5)2Ti(FC6H5)]BPh4. Most often, however, fluorocarbon substituents are used to enhance the Lewis acidity of metal centers. A premier example is "Eufod," a coordination complex of europium(III) that features a perfluoroheptyl modified acetylacetonate ligand. This and related species are useful in organic synthesis and as "shift reagents" in NMR spectroscopy.

In an area where coordination chemistry and materials science overlap, the fluorination of organic ligands is used to tune the properties of component molecules. For example, the degree and regiochemistry of fluorination of metalated 2-phenylpyridine ligands in platinum(II) complexes significantly modifies the emission properties of the complexes.[36]

The coordination chemistry of organofluorine ligands also embraces fluorous technologies. For example, triphenylphosphine has been modified by attachment of perfluoroalkyl substituents that confer solubility in perfluorohexane as well as supercritical carbon dioxide. As a specific example, [(C8F17C3H6-4-C6H4)3P.[37]

C-F bond activation

An active area of organometallic chemistry encompasses the scission of C-F bonds by transition metal-based reagents. Both stoichiometric and catalytic reactions have been developed and are of interest from the perspectives of organic synthesis and remediation of xenochemicals.[38] C-F bond activation has been classified as follows "(i) oxidative addition of fluorocarbon, (ii) M–C bond formation with HF elimination, (iii) M–C bond formation with fluorosilane elimination, (iv) hydrodefluorination of fluorocarbon with M–F bond formation, (v) nucleophilic attack on fluorocarbon, and (vi) defluorination of fluorocarbon". An illustrative metal-mediated C-F activation reaction is the defluorination of fluorohexane by a zirconium dihydride, an analogue of Schwartz's reagent:

(C5Me5)2ZrH2 + 1-FC6H13 → (C5Me5)2ZrH(F) + C6H14

Fluorocarbon anions in Ziegler-Natta catalysis

Fluorine-containing compounds are often featured in noncoordinating or weakly coordinating anions. Both tetrakis(pentafluorophenyl)borate, B(C6F5)4−, and the related tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, are useful in Ziegler-Natta catalysis and related alkene polymerization methodologies. The fluorinated substituents render the anions weakly basic and enhance the solubility in weakly basic solvents, which are compatible with strong Lewis acids.

Materials science

Organofluorine compounds enjoy many niche applications in materials science. With a low coefficient of friction, fluid fluoropolymers are used as specialty lubricants. Fluorocarbon-based greases are used in demanding applications. Representative products include Fomblin and Krytox, made by Solvay Solexis and DuPont, respectively. Certain firearm lubricants such as "Tetra Gun" contain fluorocarbons. Capitalizing on their nonflammability, fluorocarbons are used in fire fighting foam. Organofluorine compounds are components of liquid crystal displays. The polymeric analogue of triflic acid, nafion is a solid acid that is used as the membrane in most low temperature fuel cells. The bifunctional monomer 4,4'-difluorobenzophenone is a precursor to PEEK-class polymers.

Biosynthesis of organofluorine compounds

In contrast to the many naturally-occurring organic compounds containing the heavier halides, chloride, bromide, and iodide, only a handful of biologically synthesized carbon-fluorine bonds are known.[39] The most common natural organofluorine species is fluoroacetate, a toxin found in a few species of plants. Others include fluorooleic acid, fluoroacetone, nucleocidin (4'-fluoro-5'-O-sulfamoyladenosine), fluorothreonine, and 2-fluorocitrate. Several of these species are probably biosynthesized from fluoroacetaldehyde. The enzyme fluorinase catalyzed the synthesis of 5'-deoxy-5'-fluoroadenosine (see scheme to right).

History

Organofluorine chemistry began in the 1800s with the development of organic chemistry.[18][40] The first organofluorine compounds were prepared using antimony trifluoride as the F− source. The nonflammability and nontoxicity of the chlorofluorocarbons CCl3F and CCl2F2 attracted industrial attention in the 1920s. On April 6, 1938, Roy J. Plunkett a young research chemist who worked at DuPont's Jackson Laboratory in Deepwater, New Jersey, accidentally discovered polytetrafluoroethylene (PTFE).[41][42][43] Subsequent major developments, especially in the US, benefited from expertise gained in the production of uranium hexafluoride.[6] Starting in the late 1940s, a series of electrophilic fluorinating methodologies were introduced, beginning with CoF3. Electrochemical fluorination ("electrofluorination") was announced, which Joseph H. Simons had developed in the 1930s to generate highly stable perfluorinated materials compatible with uranium hexafluoride.[15] These new methodologies allowed the synthesis of C-F bonds without using elemental fluorine and without relying on metathetical methods.

In 1957, the anticancer activity of 5-fluorouracil was described. This report provided one of the first examples of rational design of drugs.[44] This discovery sparked a surge of interest in fluorinated pharmaceuticals and agrichemicals. The discovery of the noble gas compounds, e.g. XeF4, provided a host of new reagents starting in the early 1960s. In the 1970s, fluorodeoxyglucose was established as a useful reagent in 18F positron emission tomography. In Nobel Prize-winning work, CFC's were shown to contribute to the depletion of atmospheric ozone. This discovery alerted the world to the negative consequences of organofluorine compounds and motivated the development of new routes to organofluorine compounds. In 2002, the first C-F bond-forming enzyme, fluorinase, was reported.[45]

Environmental and health concerns

Only a few organofluorine compounds are acutely bioactive and highly toxic, such as fluoroacetate and perfluoroisobutene.

Some organofluorine compounds pose significant risks and dangers to health and the environment. CFCs and HCFCs (hydrochlorofluorocarbon) deplete the ozone layer and are potent greenhouse gases. HFCs are potent greenhouse gases and are facing calls for stricter international regulation and phase out schedules as a fast-acting greenhouse emission abatement measure, as are perfluorocarbons (PFCs), and sulfur hexafluoride (SF6).

Because of the compound's effect on climate, the G-20 major economies agreed in 2013 to support initiatives to phase out use of HCFCs. They affirmed the roles of the Montreal Protocol and the United Nations Framework Convention on Climate Change in global HCFC accounting and reduction. The U.S. and China at the same time announced a bilateral agreement to similar effect.[46]

Persistence and bioaccumulation

Because of the strength of the carbon–fluorine bond, many synthetic fluorocarbons and fluorocarbon-based compounds are persistent in the environment. Fluorosurfactants, such as PFOS and PFOA, are persistent global contaminants. Fluorocarbon based CFCs and tetrafluoromethane have been reported in igneous and metamorphic rock.[26] PFOS is a persistent organic pollutant and may be harming the health of wildlife; the potential health effects of PFOA to humans are under investigation by the C8 Science Panel.

See also

References
  1. Kirsch, Peer Modern fluoroorganic chemistry: synthesis, reactivity, applications. Wiley-VCH, 2004.
  2. Warren, Stuart; Wyatt, Paul (2008). Organic Synthesis: the disconnection approach (2nd ed.). Wiley. pp. 12–13.
  3. J. Lapasset; J. Moret; M. Melas; A. Collet; M. Viguier; H. Blancou (1996). "Crystal structure of 12,12,13,13,14,14,15,15,16,16,17,17,17-tridecafluoroheptadecan-1-ol, C17H23F13O". Z. Kristallogr. 211 (12): 945–946. Bibcode:1996ZK....211..945L. doi:10.1524/zkri.1996.211.12.945.CSD entry TULQOG.
  4. C.E. Smith; P.S. Smith; R.Ll. Thomas; E.G. Robins; J.C. Collings; Chaoyang Dai; A.J. Scott; S. Borwick; A.S. Batsanov; S.W. Watt; S.J. Clark; C. Viney; J.A.K. Howard; W. Clegg; T.B. Marder (2004). "Arene-perfluoroarene interactions in crystal engineering: structural preferences in polyfluorinated tolans". J. Mater. Chem. 14 (3): 413. doi:10.1039/b314094f. CSD entry ASIJIV.
  5. Milman, Oliver (22 September 2016). "100 countries push to phase out potentially disastrous greenhouse gas". The Guardian. London, UK. Retrieved 2016-09-22.
  6. G. Siegemund, W. Schwertfeger, A. Feiring, B. Smart, F. Behr, H. Vogel, B. McKusick "Fluorine Compounds, Organic" in "Ullmann's Encyclopedia of Industrial Chemistry" 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a11_349
  7. Davenport, Carol (July 23, 2016). "A Sequel to the Paris Climate Accord Takes Shape in Vienna". NYT. Retrieved 17 August 2016.
  8. "The New York Declaration of the Coalition to Secure an Ambitious HFC Amendment". Washington, DC: US Department of State. 22 September 2016. Retrieved 2016-09-22.
  9. Chris Johnston, Oliver Milman, John Vidal and agencies, "Climate change: global deal reached to limit use of hydrofluorocarbons", The Guardian, Saturday 15 October 2016 (page visited on 15 October 2016).
  10. "Climate change: 'Monumental' deal to cut HFCs, fastest growing greenhouse gases". BBC News. 15 October 2016. Retrieved 15 October 2016.
  11. "Nations, Fighting Powerful Refrigerant That Warms Planet, Reach Landmark Deal". New York Times. 15 October 2016. Retrieved 15 October 2016.
  12. Dana Lyn S. Brahms; William P. Dailey (1996). "Fluorinated Carbenes". Chemical Reviews. 96 (5): 1585–1632. doi:10.1021/cr941141k. PMID 11848805.
  13. Brunet, Vincent A.; O'Hagan, David (2008). "Catalytic Asymmetric Fluorination Comes of Age". Angewandte Chemie International Edition. 47 (7): 1179–1182. doi:10.1002/anie.200704700. PMID 18161722.
  14. Stéphane Caron; Robert W. Dugger; Sally Gut Ruggeri; John A. Ragan; David H. Brown Ripin (2006). "Large-Scale Oxidations in the Pharmaceutical Industry". Chemical Reviews. 106 (7): 2943–2989. doi:10.1021/cr040679f. PMID 16836305.
  15. Simons, J. H. (1949). "The Electrochemical Process for the Production of Fluorocarbons". Journal of the Electrochemical Society. 95 (2): 47–66. doi:10.1149/1.2776733.
  16. Vogel, A. I.; Leicester, J.; Macey, W. A. T. "n-Hexyl Fluoride". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 4, p. 525.
  17. Flood, D. T. "Fluorobenzene". Organic Syntheses; Collected Volumes, vol. 2, p. 295.
  18. William R. Dolbier Jr. (2005). "Fluorine Chemistry at the Millennium". Journal of Fluorine Chemistry. 126 (2): 157–163. doi:10.1016/j.jfluchem.2004.09.033.
  19. Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, p. 1299, ISBN 978-0-471-72091-1
  20. Wang, Chia-Lin J. (1985). "Fluorination by Sulfur Tetrafluoride". Organic Reactions. pp. 319–400. doi:10.1002/0471264180.or034.02. ISBN 978-0-471-26418-7.
  21. Aggarwal, Trapti; Verma, Akhilesh K. (2021). "Achievements in fluorination using variable reagents through a deoxyfluorination reaction". Organic Chemistry Frontiers. 8 (22): 6452–6468. doi:10.1039/D1QO00952D.
  22. Nielsen, Matthew K.; Ugaz, Christian R.; Li, Wenping; Doyle, Abigail G. (5 August 2015). "PyFluor: A Low-Cost, Stable, and Selective Deoxyfluorination Reagent". Journal of the American Chemical Society. 137 (30): 9571–9574. doi:10.1021/jacs.5b06307.
  23. Guo, Junkai; Kuang, Cuiwen; Rong, Jian; Li, Lingchun; Ni, Chuanfa; Hu, Jinbo (28 May 2019). "Rapid Deoxyfluorination of Alcohols with N‐Tosyl‐4‐chlorobenzenesulfonimidoyl Fluoride (SulfoxFluor) at Room Temperature". Chemistry – A European Journal. 25 (30): 7259–7264. doi:10.1002/chem.201901176.
  24. Pichika Ramaiah, Ramesh Krishnamurti, and G. K. Surya Prakash (1998). "1-trifluoromethyl)-1-cyclohexanol". Organic Syntheses: 232{{cite journal}}: CS1 maint: multiple names: authors list (link).
  25. Le Bars, D. (2006). "Fluorine-18 and Medical Imaging: Radiopharmaceuticals for Positron Emission Tomography". Journal of Fluorine Chemistry. 127 (11): 1488–1493. doi:10.1016/j.jfluchem.2006.09.015..
  26. Murphy CD, Schaffrath C, O'Hagan D.: "Fluorinated natural products: the biosynthesis of fluoroacetate and 4-fluorothreonine in Streptomyces cattleya" Chemosphere. 2003 Jul;52(2):455-61.
  27. Proudfoot, Alex T; Bradberry, Sally M; Vale, J Allister (2006). "Sodium Fluoroacetate Poisoning". Toxicological Reviews. 25 (4): 213–9. doi:10.2165/00139709-200625040-00002. PMID 17288493. S2CID 29189551.
  28. O'Hagan, David; Schaffrath, Christoph; Cobb, Steven L.; Hamilton, John T. G.; Murphy, Cormac D. (2002). "Biochemistry: Biosynthesis of an organofluorine molecule". Nature. 416 (6878): 279. Bibcode:2002Natur.416..279O. doi:10.1038/416279a. PMID 11907567. S2CID 4415511.
  29. Thayer, Ann M. (5 June 2006). "Fabulous Fluorine". Chemical & Engineering News. 84 (23): 15–24. doi:10.1021/cen-v084n023.p015. Retrieved 17 January 2009.
  30. Ann M. Thayer "Fabulous Fluorine" Chemical and Engineering News, June 5, 2006, Volume 84, pp. 15-24. http://pubs.acs.org/cen/coverstory/84/8423cover1.html
  31. "Phase-Out of CFC Metered-Dose Inhalers". U.S. Food and Drug Administration. Retrieved 10 September 2017.
  32. Kabayadi S. Ravikumar, Venkitasamy Kesavan, Benoit Crousse, Danièle Bonnet-Delpon, and Jean-Pierre Bégué (2003). "Mild and Selective Oxidation of Sulfur Compounds in Trifluorethanol: Diphenyl Disulfide and Methyle Phenyl Sulfoxide". Organic Syntheses. 80: 184{{cite journal}}: CS1 maint: multiple names: authors list (link).
  33. E.G. Hopea, A.P. Abbotta, D.L. Daviesa, G.A. Solana and A.M. Stuarta "Green Organometallic Chemistry" in Comprehensive Organometallic Chemistry III, 2007, Volume 12, Pages 837-864. doi:10.1016/B0-08-045047-4/00182-5
  34. J. A. Gladysz, D. P. Curran, I. T. Horváth (Eds.) "Handbook of Fluorous Chemistry", Wiley–VCH, Weinheim, 2004. ISBN 978-3-527-30617-6.
  35. Aimee Crombie, Sun-Young Kim, Sabine Hadida, and Dennis P. Curran. "Synthesis of Tris(2-Perfluorohexylethyl)tin Hydride: A Highly Fluorinated Tin Hydride with Advantageous Features of Easy Purification". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 10, p. 712.
  36. M.E. Thompson, P.E. Djurovich, S. Barlow and S. Marder "Organometallic Complexes for Optoelectronic Applications" Comprehensive Organometallic Chemistry III, 2007, Volume 12, Pages 101-194. doi:10.1016/B0-08-045047-4/00169-2
  37. J.C. Peters, J.C. Thomas "Ligands, Reagents, and Methods in Organometallic Synthesis" in Comprehensive Organometallic Chemistry III, 2007, Volume 1, Pages 59-92. doi:10.1016/B0-08-045047-4/00002-9
  38. R.N. Perutz and T. Braun "Transition Metal-mediated C–F Bond Activation" Comprehensive Organometallic Chemistry III, 2007, Volume 1, Pages 725-758. doi:10.1016/B0-08-045047-4/00028-5.
  39. O'Hagan, D.; B. Harper, David (1999). "Fluorine-Containing Natural Products". Journal of Fluorine Chemistry. 100 (1–2): 127–133. doi:10.1016/S0022-1139(99)00201-8.
  40. Okazoe, Takashi (2009). "Overview on the history of organofluorine chemistry from the viewpoint of material industry". Proceedings of the Japan Academy, Series B. 85 (8): 276–289. Bibcode:2009PJAB...85..276O. doi:10.2183/pjab.85.276. ISSN 0386-2208. PMC 3621566. PMID 19838009.
  41. "Dr. Roy J. Plunkett: Discoverer of Fluoropolymers" (PDF). The Fluoropolymers Division Newsletter (Summer): 1–2. 1994. Archived from the original (PDF) on 2003-07-09.
  42. "Roy J. Plunkett". Science History Institute. June 2016. Retrieved 21 February 2018.
  43. Center for Oral History. "Roy J. Plunkett". Science History Institute. Retrieved 21 February 2018.
  44. C. Heidelberger; N. K. Chaudhuri; P. Danneberg; D. Mooren; L. Griesbach; R. Duschinsky; R. J. Schnitzer; E. Pleven; J. Schreiner (1957). "Fluorinated Pyrimidines, A New Class of Tumour-Inhibitory Compounds". Nature. 179 (4561): 663–6. Bibcode:1957Natur.179..663H. doi:10.1038/179663a0. PMID 13418758. S2CID 4296069.
  45. O'Hagan, D; Schaffrath, C; Cobb, S. L; Hamilton, J. T; Murphy, C. D (2002). "Biochemistry: biosynthesis of an organofluorine molecule". Nature. 416 (6878): 279. Bibcode:2002Natur.416..279O. doi:10.1038/416279a. PMID 11907567. S2CID 4415511.
  46. U.S. White House Press Secretary (September 6, 2013). "United States, China, and Leaders of G-20 Countries Announce Historic Progress Toward a Global Phase Down of HFCs". whitehouse.gov (Press release). Retrieved 2013-09-16 – via National Archives.
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