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Tetrabutylammonium hexafluorophosphate nbu4npf6

Manufactured by Merck Group
Sourced in United States

Tetrabutylammonium hexafluorophosphate (nBu4NPF6) is a white crystalline salt that is commonly used as a supporting electrolyte in various electrochemical and analytical applications. It is highly soluble in polar organic solvents and has a high ionic conductivity, making it suitable for use in electrochemical cells and devices. The product is manufactured and distributed by Merck Group.

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3 protocols using tetrabutylammonium hexafluorophosphate nbu4npf6

1

Fabrication of Electrochemical Devices

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3,4-ethylenedioxythiophene (EDOT), poly(sodium 4-styrenesulfonate) (NaPSS, average Mw = 1,000,000 g/mol), and tetrabutylammonium hexafluorophosphate (nBu4NPF6) were obtained from Sigma Aldrich (Saint Louis, MO, USA). nBu4NPF6 was vacuum dried before use. Lithium perchlorate (LiClO4) and potassium chloride (KCl) were obtained from Acros Organics. Deionized water (Millipore quality) and acetonitrile (ACN, HPLC grade, Sigma Aldrich) were used as solvents.
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2

Inert Atmosphere Synthesis Protocols

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All manipulations were performed
in either an argon- or nitrogen-filled MBraun glovebox with an atmosphere
of <0.1 ppm of O2 and <0.1 ppm of H2O.
House nitrogen was purified through an MBraun HP-500-MO-OX gas purifier.
Tetrahydrofuran (THF) was predried by refluxing over potassium for
several days, distilled, and stirred over Na/K alloy for final purification.
Dimethoxyethane (DME) and toluene were dried over potassium, and nhexane was dried over calcium hydride. All
solvents were distilled under N2 from their drying agents,
and water/oxygen absence was confirmed via benzophenone solution as
an indicator within a glovebox prior to use. Deuterated solvents were
purchased from Cambridge Isotope Laboratories, dried over Na/K alloy
for several days, and filtered prior to use. Anhydrous ErCl3 was purchased from Sigma-Aldrich and used as received. 2.2.2-Cryptand
(crypt-222) was purchased from Sigma-Aldrich and crystallized from
hot nhexane prior to use. Tetrabutylammonium
hexafluorophosphate [nBu4N][PF6] was purchased from Sigma-Aldrich and crystallized several
times before use. Dibenzocyclooctatetraene (dbCOT)40 (link) and potassium graphite (KC8)41 (link) were prepared according to literature procedures. Elemental
analysis was performed at Michigan State University using a PerkinElmer
2400 Series II CHNS/O analyzer.
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3

Characterization of MOF Materials

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All solvents and commercially supplied chemicals were reagent grade and used as received without further purification. ZrCl4 (99.99%), tetrabutylammonium hexafluorophosphate (n-Bu4NPF6, for electrochemical analysis, ≥99.0%), potassium hexafluorophosphate (KPF6, ≥99.0%), 4-amino-3-hydroxybenzoic acid (97%), and fluorine-doped tin oxide (FTO) substrates (7 Ω/sq) were purchased from Sigma-Aldrich. Naphthalene-1,4,5,8-tetracarboxylic dianhydride (≥98.0%) was purchased from TCI. Glacial acetic acid, and N,N-dimethylformamide (DMF) (99.9%) were purchased from VWR. 1H-NMR spectra were measured using a JEOL 400 MHz spectrometer at 293 K. The chemical shifts given in ppm are internally referenced to the residual solvent signal. MOF samples were digested prior to NMR measurement by addition of 25 µL of HF to a suspension of 10 mg of MOF in 0.575 mL of DMSO-d6. ESI-MS data were collected on a Thermo LCQ XP Max mass spectrometer in negative mode with electrospray ionization. Electronic absorption spectra were measured using a Varian Cary 50 UV-Vis spectrophotometer. ATR-FTIR data were collected on a Bruker ALPHA FTIR Spectrometer from 4000 cm−1 to 450 cm−1 at room temperature.
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