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Cas Database

3109-63-5

3109-63-5

Identification

  • Product Name:Tetrabutylammonium hexafluorophosphate

  • CAS Number: 3109-63-5

  • EINECS:221-472-6

  • Molecular Weight:387.433

  • Molecular Formula: C16H36N.PF6

  • HS Code:29239000

  • Mol File:3109-63-5.mol

Synonyms:1-Butanaminium, N,N,N-tributyl-, hexafluorophosphate(1-);1-Butanaminium, N,N,N-tributyl-, hexafluorophosphate(1-) (1:1);

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Safety information and MSDS view more

  • Pictogram(s):,HarmfulXn

  • Hazard Codes:Xi,Xn

  • Signal Word:Warning

  • Hazard Statement:H315 Causes skin irritationH319 Causes serious eye irritation H335 May cause respiratory irritation

  • First-aid measures: General adviceConsult a physician. Show this safety data sheet to the doctor in attendance.If inhaled If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician. In case of skin contact Wash off with soap and plenty of water. Consult a physician. In case of eye contact Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician. If swallowed Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.

  • Fire-fighting measures: Suitable extinguishing media Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Wear self-contained breathing apparatus for firefighting if necessary.

  • Accidental release measures: Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. For personal protection see section 8. Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided. Pick up and arrange disposal. Sweep up and shovel. Keep in suitable, closed containers for disposal.

  • Handling and storage: Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Avoid exposure - obtain special instructions before use.Provide appropriate exhaust ventilation at places where dust is formed. For precautions see section 2.2. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.

  • Exposure controls/personal protection:Occupational Exposure limit valuesBiological limit values Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday. Eye/face protection Safety glasses with side-shields conforming to EN166. Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU). Skin protection Wear impervious clothing. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace. Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique(without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it. Respiratory protection Wear dust mask when handling large quantities. Thermal hazards

Supplier and reference price

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  • Manufacture/Brand:TRC
  • Product Description:Tetrabutylammonium Hexafluorophosphate
  • Packaging:10g
  • Price:$ 65
  • Delivery:In stock
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  • Manufacture/Brand:TCI Chemical
  • Product Description:Tetrabutylammonium Hexafluorophosphate >98.0%(T)
  • Packaging:250g
  • Price:$ 303
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  • Manufacture/Brand:TCI Chemical
  • Product Description:Tetrabutylammonium Hexafluorophosphate >98.0%(T)
  • Packaging:25g
  • Price:$ 53
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  • Manufacture/Brand:SynQuest Laboratories
  • Product Description:Tetrabutylammonium Hexafluorophosphate 98%
  • Packaging:100 g
  • Price:$ 93
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  • Manufacture/Brand:SynQuest Laboratories
  • Product Description:Tetrabutylammonium Hexafluorophosphate 98%
  • Packaging:25 g
  • Price:$ 36
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  • Manufacture/Brand:Strem Chemicals
  • Product Description:Tetrabutylammonium hexafluorophosphate, 98%
  • Packaging:5g
  • Price:$ 16
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  • Manufacture/Brand:Strem Chemicals
  • Product Description:Tetrabutylammonium hexafluorophosphate, 98%
  • Packaging:25g
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  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Tetrabutylammonium hexafluorophosphate for electrochemical analysis, ≥99.0%
  • Packaging:100g
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  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Tetrabutylammonium hexafluorophosphate for electrochemical analysis, ≥99.0%
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  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Tetrabutylammonium hexafluorophosphate purum, ≥98.0% (CHN)
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Relevant articles and documentsAll total 21 Articles be found

Electrochemistry and ion-sensing properties of calix[4]arene derivatives

Chen, Shanshan,Webster, Richard D.,Talotta, Carmen,Troisi, Francesco,Gaeta, Carmine,Neri, Placido

, p. 7036 - 7043 (2010)

The cyclic voltammetric properties of several substituted calix[4]arenes were examined in acetonitrile and dichloromethane. The compounds that contained one phenolic group in the macrocyclic cavity were able to be electrochemically oxidised at positive potentials. In acetonitrile, cyclic voltammetry experiments indicated that the phenolic compounds were oxidised in a two-electron (one-proton) process over all measured scan rates (up to 50 V s-1), while in dichloromethane, the oxidation process occurred by one-electron at scan rates ≥5 V s-1, to most likely form the radical cations. In both solvents, longer timescale (minutes to hours) controlled potential coulometry experiments indicated that the oxidation process occurred by two-electrons per molecule, to form reactive diamagnetic cations that could not be reduced back to the starting materials under electrolysis conditions. The ion-sensing properties of the compounds were investigated in polymer membrane ion-selective electrodes and it was found that they responded reversibly in a Nernstian fashion to Groups 1 and 2 metals and had the highest selectivity to the cesium cation.

Competing hydrogen-bonding, decomposition, and reversible dimerization mechanisms during the one- and two-electron electrochemical reduction of retinal (Vitamin A)

Tan, Ying Shan,Yue, Yanni,Webster, Richard D.

, p. 9371 - 9379 (2013)

Retinal (R) can be sequentially voltammetrically reduced in CH 3CN in two one-electron processes to form first the anion radical (Ra?¢-) at -1.75 (?±0.04) V vs Fc/Fc+ (Fc = ferrocene) then the dianion (R2-) at -

METAL COMPLEXES WITH TETRAPYRROLE LIGANDS. 50. REDOX POTENTIALS OF SANDWICHLIKE METAL BIS(OCTAETHYLPORPHYRINATES) AND THEIR CORRELATION WITH RING-RING DISTANCES

Buchler, Johann W.,Scharbert, Bernd

, p. 4272 - 4276 (1988)

On the basis of prior work describing the synthesis and structure of sandwichlike metal bis(porphyrinates) M(OEP)2 (I:M=Y, La, ..., Lu, except Pm), the electron-transfer reactions of these double-deckers are presented.Apart from the CeIV complex Ce(OEP)2 (1c), all the other species contain MIII ions that are not affected in the redox reactions.The neutral MIII complexes 1 are porphyrin ?-radicals yielding the porphyrin ?-diradical cations + (2) upon reversible one-electron oxidation and the monoanions - (3) or the porphyrin ?-radical dianions 2- (4) upon reversible one- or two-electron reduction.Ce(OEP)2 (1c) is reversibly oxidized to the porphyrin ?-radical cation + (2c).The quasi-reversible reduction of (1c) gives the anion - (3c) with CeIII.For the neutral MIII complexes 1, the energies of the near-infrared absorption bands and the redox potentials for the processes 12 are correlated with the ionic radii rI. of the tervalent central ions MIII.A decrease of the ring oxidation potentials parallels a decrease of the ionic radii and, hence, the ring-ring distances in the double-deckers.

Electrochemical/chemical oxidation of bisphenol A in a four-electron/two- proton process in aprotic organic solvents

Chan, Ya Yun,Yue, Yanni,Li, Yongxin,Webster, Richard D.

, p. 287 - 294 (2013)

The electrochemical behavior of bisphenol A (BPA) was examined using cyclic voltammetry, bulk electrolysis and chemical oxidation in aprotic organic solvents. It was found that BPA undergoes a chemically irreversible voltammetric oxidation process to form compounds that cannot be electrochemically converted back to the starting materials on the voltammetric timescale. To overcome the effects of electrode fouling during controlled potential electrolysis experiments, NO+ was used as a one-electron chemical oxidant. A new product, hydroxylated bisdienone was isolated from the chemical oxidation of BPA with 4 mol equiv of NO+SbF6- in low water content CH3CN. The structure of the cation intermediate species was deduced and it was proposed that BPA is oxidized in a four-electron/two-proton process to form a relatively unstable dication which reacts quickly in the presence of water in acetonitrile (in a mechanism that is similar to phenols in general). However, as the water content of the solvent increased it was found that the chemical oxidation mechanism produced a nitration product in high yield. The findings from this study provide useful insights into the reactions that can occur during oxidative metabolism of BPA and highlight the possibility of the role of a bisdienone cation as a reactive metabolite in biological systems.

Phenylcyanamidoruthenium scorpionate complexes

Harb, Carmen,Kravtsov, Pavel,Choudhuri, Mohommad,Sirianni, Eric R.,Yap, Glenn P.A.,Lever,Crutchley, Robert J.

, p. 1621 - 1630 (2013)

Nine [Ru(Tp)(dppe)L] complexes, where Tp is hydrotris(pyrazol-1-yl)borate, dppe is ethylenebis(diphenylphosphine), and L is (4-nitrophenyl)cyanamide (NO2pcyd-), (2-chlorophenyl)cyanamide (2-Clpcyd -), (3-chlorophenyl)cyanamide (3-Clpcyd-), (2,4-dichlorophenyl)cyanamide (2,4-Cl2pcyd-), (2,3-dichlorophenyl)cyanamide (2,3-Cl2pcyd-), (2,5-dichlorophenyl)cyanamide (2,5-Cl2pcyd-), (2,4,5-trichlorophenyl)cyanamide (2,4,5-Cl3pcyd-), (2,3,5,6-tetrachlorophenyl)cyanamide (2,3,5,6-Cl4pcyd-), and (pentachlorophenyl)cyanamide (Cl5pcyd-), and the dinuclear complex [{Ru(Tp)(dppe)}2(μ-adpc)], where adpc 2- is azo-4,4-diphenylcyanamide, have been prepared and characterized. The crystal structures of [Ru(Tp)(dppe)(Cl5pcyd)] and [{Ru(Tp)(dppe)}2(μ-adpc)] reveal the RuII ion to occupy a pseudooctahedral coordination sphere in which the cyanamide ligand coordinates to RuII by its terminal nitrogen atom. For both complexes, the cyanamide ligands are planar, indicating significant π mixing between the cyanamide and phenyl moieties as well as the azo group in the case of adpc2-. The optical spectra of the nominally ruthenium(III) species [Ru(Tp)(dppe)L]+ were obtained through spectroelectrochemistry measurements and showed an intense near-IR absorption band. Time-dependent density functional theory calculations of these species revealed that oxidation of the ruthenium(II) species led to species where partial oxidation of the cyanamide ligand had occurred, indicative of noninnocent character for these ligands. The spin densities reveal that while the 3-Clpycd species has substantial RuII(3-Clpycd0) character, the Cl5pycd species is a much more localized ruthenium(III) complex of the Cl5pycd monoanion. Some bond order and charge distribution data are derived for these ruthenium(III) species. The near-IR band is assigned as a quite complex mixture of d-d, 4dπ to L(NCN) MLCT, and L(NCN) to Ru 4d LMCT with even a scorpionate ligand component. Spectroelectrochemistry was also performed on [{Ru(Tp)(dppe)} 2(μ-adpc)] to generate the mixed-valence state. The intense intervalence transition that is observed in the near-IR is very similar to that previously reported for [{Ru(trpy)(bpy)}2(μ-adpc)]2+, where trpy is 2,2′:6′,2″-terpyridine and bpy is 2,2′-bipyridine, and by analogy identifies [{Ru(Tp)(dppe)} 2(μ-adpc)]+ as a delocalized mixed-valence complex.

PGSE NMR diffusion overhauser studies on [Ru(Cp*)(η6- arene)][PF6], plus a variety of transition-metal, inorganic, and organic salts: An overview of ion pairing in dichloromethane

Moreno, Aitor,Pregosin, Paul S.,Veiros, Luis F.,Albinati, Alberto,Rizzato, Silvia

, p. 5617 - 5629 (2008)

PGSE diffusion, 1F, 1H HOESY and 13CNMR studies for a series of [Ru(Cp*)(η6-arene)][PF6] (1) salts are presented. The solid-state structure of [Ru(Cp*) (η6-fluorobenzene)][PF6] (1c) is reported. The extent of the ion pairing and the relative positions of the ions are shown to depend on the arene. For the solvent dichloromethane, new and literature PGSE data for PF6- salts of transition-metal, inorganic, and organic salts are compared. Taken together, these new results show that the charge distribution and the ability of the anion to approach the positively charged positions (steric effects due to molecular shape) are the determining factors in deciding the amount of ion pairing. DFT calculations of the charges in four salts of type 1, as well as in a variety of other salts, using a natural population analysis (NPA), support this view. This represents the first attempt, using experimental data, to understand, correlate, and partially explain the various degrees of ion pairing in a widely different collection of salts.

Thermal stability of quaternary ammonium hexafluorophosphates and halides

Zhuravlev,Nikol'skii,Voronchikhina

, p. 824 - 830 (2013)

Thermal decomposition of hexafluorophosphates of short-chain tetraalkylammonium salts of the general formula R3R'NPF6, where R3 = R' = CH3, C2H5, C 4H9; R3 = C2H5, R' = CH2C6H6 or CH2CH=CH2, was studied by thermal gravimetric analysis. Measurements were performed in air in the temperature interval 20-500°N. The thermal stability of halides with the same cations in the same temperature interval was studied for comparison. The effect of cation on the thermal stability of the halides and hexafluorophosphates was examined. The mechanism of thermal decomposition of quaternary ammonium hexafluorophosphates was suggested.

Tetracyanido(difluorido)phosphates M+[PF2(CN)4]-

Bresien, Jonas,Ellinger, Stefan,Harloff, J?rg,Schulz, Axel,Sievert, Katharina,Stoffers, Alrik,T?schler, Christoph,Villinger, Alexander,Zur T?schler, Cornelia

, p. 4474 - 4477 (2015)

The systematic study of the reaction of M[PF6] salts and Me3SiCN led to a synthetic method for the synthesis and isolation of a series of salts containing the unprecedented [PF2(CN)4]- ion in good yields. The reaction temperature, pressure, and stoichiometry were optimized. The crystal structures of M[PF2(CN)4] (M=[nBu4N]+, Ag+, K+, Li+, H5O2+) were determined. X-ray crystallography showed the exclusive formation of the cis isomer in accord with 31P and 19F solution NMR spectroscopy data. Starting with the K[PF2(CN)4] the room temperature ionic liquid EMIm[PF2(CN)4] was prepared exhibiting a rather low viscosity.

Deoxygenative Fluorination of Phosphine Oxides: A General Route to Fluorinated Organophosphorus(V) Compounds and Beyond

Bornemann, Dustin,Brüning, Fabian,Grützmacher, Hansj?rg,Guan, Liangyu,Küng, Sebastian,Pitts, Cody Ross,Togni, Antonio,Trapp, Nils,Wettstein, Lionel

supporting information, p. 22790 - 22795 (2020/10/06)

Fluorinated organophosphorus(V) compounds are a very versatile class of compounds, but the synthetic methods available to make them bear the disadvantages of 1) occasional handling of toxic or pyrophoric PIII starting materials and 2) a dependence on hazardous fluorinating reagents such as XeF2. Herein, we present a simple solution and introduce a deoxygenative fluorination (DOF) approach that utilizes easy-to-handle phosphine oxides as starting materials and effectively replaces harsh fluorinating reagents by a combination of oxalyl chloride and potassium fluoride. The reaction has proven to be general, as R3PF2, R2PF3, and RPF4 compounds (as well as various cations and anions derived from these) are accessible in good yields and on up to a multi-gram scale. DFT calculations were used to bolster our observations. Notably, the discovery of this new method led to a convenient synthesis of 1) new difluorophosphonium ions, 2) hexafluorophosphate salts, and 3) fluorinated antimony- and arsenic- compounds.

Lewis Acidity Scale of Diaryliodonium Ions toward Oxygen, Nitrogen, and Halogen Lewis Bases

Legault, Claude Y.,Mayer, Robert J.,Mayr, Herbert,Ofial, Armin R.

supporting information, (2020/03/13)

Equilibrium constants for the associations of 17 diaryliodonium salts Ar2I+X- with 11 different Lewis bases (halide ions, carboxylates, p-nitrophenolate, amines, and tris(p-anisyl)phosphine) have been investigated by titrations followed by photometric or conductometric methods as well as by isothermal titration calorimetry (ITC) in acetonitrile at 20 °C. The resulting set of equilibrium constants KI covers 6 orders of magnitude and can be expressed by the linear free-energy relationship lg KI = sI LAI + LBI, which characterizes iodonium ions by the Lewis acidity parameter LAI, as well as the iodonium-specific affinities of Lewis bases by the Lewis basicity parameter LBI and the susceptibility sI. Least squares minimization with the definition LAI = 0 for Ph2I+ and sI = 1.00 for the benzoate ion provides Lewis acidities LAI for 17 iodonium ions and Lewis basicities LBI and sI for 10 Lewis bases. The lack of a general correlation between the Lewis basicities LBI (with respect to Ar2I+) and LB (with respect to Ar2CH+) indicates that different factors control the thermodynamics of Lewis adduct formation for iodonium ions and carbenium ions. Analysis of temperature-dependent equilibrium measurements as well as ITC experiments reveal a large entropic contribution to the observed Gibbs reaction energies for the Lewis adduct formations from iodonium ions and Lewis bases originating from solvation effects. The kinetics of the benzoate transfer from the bis(4-dimethylamino)-substituted benzhydryl benzoate Ar2CH-OBz to the phenyl(perfluorophenyl)iodonium ion was found to follow a first-order rate law. The first-order rate constant kobs was not affected by the concentration of Ph(C6F5)I+ indicating that the benzoate release from Ar2CH-OBz proceeds via an unassisted SN1-type mechanism followed by interception of the released benzoate ions by Ph(C6F5)I+ ions.

Gold(I) Complexes Nuclearity in Constrained Ferrocenyl Diphosphines: Dramatic Effect in Gold-Catalyzed Enyne Cycloisomerization

Nguyen, Tuan-Anh,Roger, Julien,Nasrallah, Houssein,Rampazzi, Vincent,Fournier, Sophie,Cattey, Hélène,Sosa Carrizo, E. Daiann,Fleurat-Lessard, Paul,Devillers, Charles H.,Pirio, Nadine,Lucas, Dominique,Hierso, Jean-Cyrille

supporting information, p. 2879 - 2885 (2020/08/13)

Di-tert-butylated-bis(phosphino)ferrocene ligands bearing phosphino substituents R (R=phenyl, cyclohexyl, iso-propyl, mesityl, or furyl) allow tuning the selective formation of Au(I) halide complexes. Thus, dinuclear linear two-coordinate, but also rare mononuclear trigonal three-coordinate and tetrahedral four-coordinate complexes were formed upon tuning of the conditions. Both Au(I) chloride and rarer Au(I) iodide complexes were synthesized, and their X-ray diffraction analysis are reported. The significance of the control of structure and nuclearity in Au(I) complexes is further illustrated herein by its strong effect on the efficiency and selectivity of gold-catalysed cycloisomerization. Cationic linear digold(I) bis(dicyclohexylphosphino) ferrocenes outperform other catalysts in the demanding regioselective cycloisomerization of enyne sulphonamides into cyclohexadienes. Conversely, tetrahedral and trigonal cationic monogold(I) complexes were found incompetent for enyne cycloaddition. We used the two-coordinate linear electron-rich Au(I) complex 2 b (R=Cy) to extend the scope of selective intramolecular cycloaddition of different 1,6-enyne sulfonylamines with high activity and excellent selectivity to the endo cyclohexadiene products.

Lewis Acid Catalyzed Synthesis of Cyanidophosphates

Bl?sing, Kevin,Ellinger, Stefan,Harloff, J?rg,Schulz, Axel,Sievert, Katharina,T?schler, Christoph,Villinger, Alexander,Zurt?schler, Cornelia

supporting information, p. 4175 - 4188 (2016/03/16)

Salts containing new cyanido(fluorido)phosphate anions of the general formula [PF6-n(CN)n]- (n=1-4) were synthesized by a very mild Lewis-acid-catalyzed synthetic protocol and fully characterized. All [PF6-n(CN)n]- (n=1-4) salts could be isolated on a preparative scale. It was also possible to detect the [PF(CN)5]- but not the [P(CN)6]- anion. The best results with respect to purity, yield, and low cost were obtained when the F-/CN- substitution reactions were carried out in ionic liquids. Cyanido(fluorido)phosphates: Salts containing [PF6-n(CN)n]- (n=1-4) ions were isolated on a preparative scale by utilizing Lewis acids (LA) catalysts under mild conditions (see equation). The best results with respect to purity, yield, and low cost were obtained when the F-/CN- substitution reactions were carried out in ionic liquids.

Process route upstream and downstream products

Process route

tetrabutylammomium bromide
1643-19-2

tetrabutylammomium bromide

tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
With trimethyl phosphite; hexafluorophosphoric acid; at 0 - 60 ℃; for 15h; Inert atmosphere; neat (no solvent);
96%
With potassium hexafluorophosphate; In dichloromethane; water; at 20 ℃; for 24h;
88%
With potassium hexafluorophosphate; In dichloromethane; water; at 20 ℃; for 24h;
88%
With potassium hexafluorophosphate; In dichloromethane; water; at 25 ℃; for 24h;
88%
With ammonium hexafluorophosphate; In acetone; Heating;
With potassium hexafluorophosphate;
With hexafluorophosphoric acid;
With potassium hexafluorophosphate; In water;
tetrabutyl-ammonium chloride
1112-67-0

tetrabutyl-ammonium chloride

phosphonic acid diethyl ester
762-04-9

phosphonic acid diethyl ester

tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
phosphonic acid diethyl ester; With potassium fluoride; oxalyl dichloride; In acetonitrile; at 20 ℃; Glovebox; Sealed tube; Inert atmosphere;
tetrabutyl-ammonium chloride; In water; at 20 ℃; for 0.166667h; Glovebox; Sealed tube; Inert atmosphere;
59%
tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
With silver(I) hexafluorophosphate; In dichloromethane; acetonitrile; at 20 ℃; for 10h; Darkness;
92%
tetra(n-butyl)ammonium hydroxide
2052-49-5

tetra(n-butyl)ammonium hydroxide

tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
With hexafluorophosphate; In water;
With hexafluorophosphoric acid; In water;
With hexafluorophosphoric acid; In water; Inert atmosphere; Schlenk technique;
potassium hexafluorophosphate
17084-13-8

potassium hexafluorophosphate

tetrabutyl-ammonium chloride
1112-67-0

tetrabutyl-ammonium chloride

tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
In water; for 24h;
ammonium hexafluorophosphate

ammonium hexafluorophosphate

tetrabutylammomium bromide
1643-19-2

tetrabutylammomium bromide

tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
In not given; recrystn.(ethanol/water), drying (vacuo, 24 h, 80°C);
ammonium hexafluorophosphate

ammonium hexafluorophosphate

tetrabutylammomium bromide
1643-19-2

tetrabutylammomium bromide

tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
In water;
C<sub>15</sub>H<sub>16</sub>IO<sub>3</sub><sup>(1+)</sup>*F<sub>6</sub>P<sup>(1-)</sup>

C15H16IO3(1+)*F6P(1-)

tetrabutylammonium benzoate
18819-89-1

tetrabutylammonium benzoate

C<sub>25</sub>H<sub>27</sub>IO<sub>8</sub>

C25H27IO8

tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
In acetonitrile; at 20 ℃; Equilibrium constant; Inert atmosphere;
C<sub>15</sub>H<sub>16</sub>IO<sub>3</sub><sup>(1+)</sup>*F<sub>6</sub>P<sup>(1-)</sup>

C15H16IO3(1+)*F6P(1-)

tetra-n-butylammonium p-nitrophenoxide
3002-48-0

tetra-n-butylammonium p-nitrophenoxide

C<sub>24</sub>H<sub>26</sub>INO<sub>9</sub>

C24H26INO9

tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
In acetonitrile; at 20 ℃; Equilibrium constant; Inert atmosphere;
tetrabutyl-ammonium chloride
1112-67-0

tetrabutyl-ammonium chloride

C<sub>15</sub>H<sub>16</sub>IO<sub>3</sub><sup>(1+)</sup>*F<sub>6</sub>P<sup>(1-)</sup>

C15H16IO3(1+)*F6P(1-)

C<sub>18</sub>H<sub>22</sub>ClIO<sub>6</sub>

C18H22ClIO6

tert-butylammonium hexafluorophosphate(V)
3109-63-5

tert-butylammonium hexafluorophosphate(V)

Conditions
Conditions Yield
In acetonitrile; at 20 ℃; Equilibrium constant; Thermodynamic data; Inert atmosphere;

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