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21 protocols using k2co3

1

Synthesis of Alkali Niobium Tantalum Antimonite Perovskite

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The precursors used were Nb2O5 (99.9% purity, Sigma-Aldrich, St. Louis, MO, USA), Ta2O5 (99.0% purity, Sigma-Aldrich), Sb2O5 (99.9% purity, Alfa Aesar, Haverhill, MA, USA), Na2CO3 (99.5% purity, Panreac M&E, Barcelona, Spain), K2CO3 (99.0% purity, Fisher Scientific, Hampton, NH, USA) and Li2CO3 (99.5% purity, Panreac M&E). These precursors were attrition-milled individually in a Fritsch Pulverisette 7 planetary ball using ZrO2 stabilized with Y2O3 balls in ethanol during 2 h. This grinding step homogenized the particle size of the different powders between 2 and 10 μm. The powders obtained were oven dried at 80 °C for 24 h, were mixed according to the stoichiometry of the (K0.44Na0.52Li0.04)(Nb0.82Ta0.10Sb0.04)O3 formula and were attrition-milled again for 2 h.
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2

Facile Synthesis of Multifunctional Nanoparticles

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Iron(III) chloride hexahydrate (FeCl3·6H2O), gold(III) chloride trihydrate (HAuCl4·3H2O), poly(acrylic acid) (PAA, average M.W. 1800), tetraethyl orthosilicate (TEOS), formaldehyde (HCHO), 3-aminopropyltriethoxysilane (APTES), tetrakis-(hydroxymethyl)phosphonium chloride (THPC), 1-octanethiol, poly(ethylene glycol) methyl ether thiol (PEG-SH), poly(ethylene glycol) diacrylate (PEGDA, average Mn 575), and phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (photoinitiator) were purchased from Sigma-Aldrich. NH4OH solution (28%), NaOH, K2CO3, and CS2 were purchased from Fisher Scientific. Ethanol (200 proof) is purchased from Decon Laboratories Inc. Polyvinylpyrrolidone (PVP, K12, average M.W. 3500) is purchased from Acros Organics. All the chemicals were used as received.
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3

Bioactive 1393 Silicate Glass Fiber Synthesis

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The bioactive 1393 silicate glass (53 SiO2-20 CaO-6 Na2O-4 P2O5-12 K2O-5 MgO wt%) was prepared through standard procedures reported elsewhere [26 (link)]. In short, the powdered CaCO3, Na2CO3, MgCO3, K2CO3, SiO2, and CaHPO4·2H2O (Fisher Scientific, St. Louis, MO, USA) were mixed thoroughly for 30 min. This batch was melted in a platinum crucible and an electric furnace at 1350 °C for 2 h until homogeneously melted. Once melted, a silica rod was dipped into the solution and raised to produce initial fiber formation. These fibers were pulled by hand, annealing instantly at room temperature. Fibers that were less than 150 μm without bead formation were used in this study.
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4

Acid-Catalyzed Compound 1 Transformation

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Compound 1 (5.0 mg, 7.3421 μMol) was dissolved in 5% HCl-MeOH (3 mL) (HCl, 37% produce by Fisher Scientific and MeOH obtained from SOLEVO-Cameroon) and refluxed for 14 h at 70˚C. The reaction was monitored using TLC analysis. At the end of the reaction, the mixture obtained was extracted with methylene chloride (CH 2 Cl 2 obtained from SOLEVO-Cameroon) after neutralization with dilute potassium carbonate (K 2 CO 3 , produce by Fisher Scientific with 99.9% purity). The organic phase was separated and concentrated to yield 2.1 mg.
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5

Synthesis of Benzonitrile Derivative

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Reagent grade 2-(bromomethyl) benzonitrile and 8-hydroxyquinoline were purchased from Sigma Aldrich. Solvents, K2CO3, potassium iodide, NaOH and Cu(NO3)2·3H2O were procured from ThermoFisher scientific, India.
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6

Bioglass Disc Preparation and Surface Modification

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S53P4 and 13-93B20 BaG were prepared from analytical grade K2CO3 (Alfa Aesar, Thermo Fischer, Kandel, Germany),
Na2CO3, NH4H2PO4, (CaHPO4)(2(H2O)), CaCO3, MgO,
H3BO3 (Sigma-Aldrich, Saint-Louis, MS), and
Belgian quartz sand. The nominal oxide compositions of the experimental
BaGs are presented in Table 1 in mol %.
The reagents
were melted in a platinum crucible at 1450 °C
in an electrical furnace. The molten glass was then cast into a preheated
graphite mold to obtain a rod with a diameter of 14 mm. The glass
rods were then annealed overnight at 500 °C and let to cool down
to room temperature. The rods were then cut into 2 mm thick discs
and polished with SiC paper (grit #320, #500, #800, #1200, #2400,
and #4000, from Struers, Copenhagen, Denmark). All samples were dried
and kept in a desiccator until further use.
Membranes were directly
deposited onto untreated or surface-modified
BaG discs. Discs with both BaGs composition were surface treated by
either silanization or conditioning. The surface treatment protocols
are as follows.
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7

Colorimetric Enzyme Activity Assay

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Tannic acid (TA, Mw = 1701.23 g·mol−1, CAS 1401-55-4), ferroceneboronic acid ≥ 95% (FcB(OH)2, Mw = 229.85 g·mol−1, CAS 12152-94-2), glucose oxidase from Aspergillus Niger sp. Type X-S (GOx, ~168 U·mg−1, Mw = 160 kDa, G7141, CAS 9001-37-0), horseradish peroxidase (HRP, ~250 U·mg−1, Mw = 44 kDa, CAS 9003-99-0), hydrogen peroxide solution 30 wt.% (H2O2, Mw = 34.01 g·mol−1, CAS 7722-84-1), Bradford reagent (reference B6916), and phosphate buffered saline tablets were purchased from Sigma-Aldrich (St. Louis, MO, USA). Ferrocene methanol (FcOH ≥ 95%, Mw = 216.1 g·mol−1, CAS 1273-86-5) was retrieved from FluoroChem (Hadfield, UK). Hydrogen tetrachloroaurate(III) hydrate (HAuCl4, Mw = 393.83 g·mol−1, CAS 27988-77-8), d-(+)-glucose anhydrous 99% (Mw = 180.16 g·mol−1, CAS 50-99-7), and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS 98 %, Mw = 548.68 g·mol−1, CAS 30931-67-0) were purchased from Alfa Aesar (Haverhill, MA, USA). Sodium chloride ≥99.5% (NaCl, Mw = 58.44 g·mol−1, CAS 7631-99-4), and potassium carbonate ≥99.5% (K2CO3, Mw) =138.21 g·mol−1, CAS 209-529-3) were purchased from Fischer (Pittsburgh, PA). All chemicals were used as received and solution were prepared using Milli-Q water with 18.2 MΩ·cm resistivity.
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8

Synthesis of Benzonitrile Derivative

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Reagent-grade 2-(bromomethyl) benzonitrile and 8-hydroxyquinoline were purchased from Sigma Aldrich. K2CO3, Cu(NO3)2·3H2O, potassium iodide and NaOH were obtained from Thermo Fisher scientific, India. Solvents were purified prior to use following standard methods.
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9

Synthesis and Characterization of Polystyrene-Based Polymers

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Polystyrene (PS, Mn ∼ 170 kg
mol–1, PDI = 2.06, Sigma-Aldrich),
2-(piperidine-4-yl)propan-2-ol (PiptOH, 95%, Fluorochem),
1,1,1-trifluoroacetic acid (TFA, 99%, Acros), 1,1,1-trifluoromethanesulfonic
acid (TFSA, 99%, Acros), iodomethane (99%, Sigma-Aldrich), K2CO3 (99%, Acros), 1,5-dibromopentane (97%, Sigma-Aldrich),
1,4-dibromobutane (99%, Sigma-Aldrich), N-ethyldiisopropylamine
(DIPEA, 99%, Sigma-Aldrich), isopropanol (IPA, reagent grade, VWR),
diethyl ether (reagent grade, VWR), N-methyl-2-pyrrolidone
(NMP, reagent grade, Acros), dimethyl sulfoxide (DMSO, reagent grade,
VWR), NaBr (99%, Sigma-Aldrich), NaOH (99%, pellets, VWR), chloroform-d (99.8 atom % D, Sigma-Aldrich), and DMSO-d6 (99.96 atom % D, Sigma-Aldrich) were all used as received.
Dichloromethane and toluene were dried in an MBraun dry solvent dispenser
system (MB-SPS 800) prior to use.
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10

Synthetic Procedures and Characterization

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N,N-Dimethylethanolamine (99%), ethanol (99.9%), ethyl iodide (98%), 2-propanol (99%), HCl conc. (35%), NaNO2 (99%), phenol (98%) K2CO3 (99.5%), Na2CO3 (99.5%), NaOH (98%), 1-bromododecane (99%), 1-bromoheptane (99%), 1-bromooctane (99%) and 1,6-dibromohexane (99%) were purchased from Acros Organics and used without further purification. Petroleum ether (b.p. 60–90 °C), acetonitrile (99.9%), dichloromethane (99.9%), acetone (99%) and ethyl acetate (99%) were commercial products obtained from Acros Organics. 1H NMR (400 MHz) and 13C NMR (100 MHz) were recorded on a Bruker 400 MHz Ultrashield™ spectrometer. Elemental analysis was performed using a CHN elemental analyser.
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