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44 protocols using 4 nitroaniline

1

Synthesis and Characterization of N-doped Reduced Graphene Oxide

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Graphite powder (99.99% -trace metal basis), sodium nitrate (99%), potassium permanganate (99%), 4-nitroaniline (≥99%), 4-aminophenol (≥99%) and 4-nitro-ο-phenylenediamine (≥99%) were purchased from Sigma-Aldrich, Johannesburg, South Africa. These chemicals were of analytical grade and were used without further purification. Hydrogen peroxide (100%) was purchased from Merck Laboratory Supplies, Johannesburg, South Africa. Sulfuric acid (98%) was purchased from Promark Chemicals, Johannesburg, South Africa. Double distilled water was obtained from a double distiller, Glass Chem water distiller model Ws4lcd was supplied by Shalom Laboratory Supplies, Durban, South Africa. A gas mixture of 10% hydrogen in argon (v/v) was purchased from Afrox Limited Gas Co., Durban, South Africa. Weighing of N-rGO was done on an electronic weighing balance, Mettler AE 200, Mundelein, IL USA. Ultrasonication was performed in a digital ultrasonic water bath (400 W) obtained from Shalom Laboratory Supplies, Durban, South Africa.
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2

Efficient Extraction of Roasted Onion Leaves

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Chemicals including CA (≥97%), RA (≥97%), BL (98%), and ML (97%) were purchased from Aladdin Biochemical Technology Co., Ltd. (Shanghai, China). Polyethylene glycol (number average molecular weight, 400) (PEG-400) was supplied by Yantian Biotechnology Co., Ltd. (Shanghai, China). The IL, [C4mim]PF6 (99%) was obtained from the Lanzhou Institute of Chemical Physics of the Chinese Academy of Sciences (Lanzhou, China). Reichardt’s dye (RD, 90%) and 4-nitroaniline (NA, ≥99%) were supplied by Sigma-Aldrich Co., (St. Louis, MO, USA); N,N-diethyl-4-nitroaniline (DENA, 97%) was obtained from Fluorochem Ltd., (Hadfield, UK). The macroporous resins CAD-40 (polar resin, specific surface area: 450–500 m2 g−1, particle size: 60–16 meshes) and HP-20 (non-polar resin, specific surface area: 550–600 m2 g−1, particle size: 60–16 meshes) were supplied by Xinhu Laboratory Equipment Co., Ltd. (Shanghai, China). All the other reagents are of analytical grade and were used as received. Dried ROLs were supplied by Haoruijia Biotechnology Co., Ltd. (Chengdu, China) and crushed into fine powers (100 meshes) before use. The extract of the ROLs was prepared using 45% PEG-400 as the extraction solvent containing 4.3% H3PO4 [13 (link)].
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3

Reagent Sources for Immunoassay Development

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NIC, 4-nitroaniline, 2-nitroaniline, 3-nitroaniline, N-(4-nitrophenyl) propionamide, H-Val-pNA HCl, L-argininep-nitroanilide dihydrochloride, 4-nitrophenethylamine hydrochloride, N-methyl-4-nitrophenethylamine hydrochloride, H-Ala-pNA HCl, N, N-dimethyl-4-nitroaniline, H-Glu-pNA, halofuginone, toltrazuril, 1,3-diphenylguanidine, ronidazole, and dinitolmide were obtained from Sigma-Aldrich (St. Louis, MO, USA) (Figure 1). The coating antigen (DNC-4-BSA) and mAb 3B4 were acquired from China Agricultural University (Qianqian Tang May 2018). For other reagents materials were shown in the Supplementary Materials part.
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4

Synthesis of 4-Nitrobenzenediazonium Tosylate

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Acetic acid (reagent grade, ≥99%), diethyl ether, deionized water, methanol (puriss. p.a., absolute, ≥99.8% (GC)), p-toluenesulfonic acid monohydrate (ACS reagent, ≥98.5%), tert-butyl nitrite (90%), 4-nitroaniline (≥99%), and PEDOT:PSS water suspension was supplied from Sigma-Aldrich. 4-Nitrobenzenediazonium tosylate was synthesized according to the published procedure.29 (link)
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5

Soybean Oil and Waste Snail Shell Characterization

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Soybean oil was purchased from the local market in Silchar, Assam, India and its physical properties and compositions are listed in Table 1 of the ESI. Waste snail shells (Pila spp.) were procured from Mizoram, India. Methanol of analytical reagent (AR) grade was acquired from Merck, India. Double distilled water was used throughout the experiments. Bromothymol blue (pKa = 7.2), phenolphthalein (pKa = 9.8), indigo carmine (pKa = 12.2), 2,4-dinitroaniline (pKa = 15.0) and 4-nitroaniline (pKa = 18.4) were purchased from Sigma Aldrich.
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6

Spectroscopic Analysis of Nitroaniline Dyes

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p-Nitroanisole (1) (purity > 99%) was purchased from Sigma-Aldrich. The displacements for this dye are expected to characterize interactions with dye dipoles and induced dipoles.22
N,N-diethyl-4-nitroaniline (2) (purity > 99 %) was purchased from Fluorochem. The electronic transitions for dye (2) are expected to be more sensitive to solvent-donor to dye-acceptor hydrogen bond interactions.23 4-nitroaniline (3) (purity > 99 %) was purchased from Sigma-Aldrich. The electronic transitions for dye (3) are expected to be more sensitive to solvent-acceptor to dye-donor hydrogen bond interactions.22
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7

Synthesis of Substituted Anilines

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4-Nitroaniline (Sigma Aldrich), 3-Nitroaniline(Alfa Aesar), 3-(trifluoromethyl) aniline, 4-Nitro-2-(trifluoromethyl) aniline(Alfa Aesar), 3,5-dinitro aniline (Sigma Aldrich), 2,4-dinitro aniline (Sigma Aldrich), Sodium Azide (Sigma Aldrich), Copper Sulphate and Sodium ascorbate were used as received. Dichloromethane (Merck) was distilled. Triethyl amine was also distilled. Acryloyl chloride(Alfa Aesar) were used under inert conditions. AIBN (Sigma Aldrich) as obtained. All the solvents were purified by distillation prior to their use.
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8

Photocatalytic Degradation of Phenol

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All chemicals used for the synthesis of all materials, photocatalytic degradation and the determination of phenol were of analytical-reagent grade (pro analysis) and used as obtained. Melamine, dicyandiamide, guanidine hydrochloride, 4-nitroaniline and amoxicillin were purchased from Sigma-Aldrich (Darmstadt, Germany). Phenol and Rhodamine B were obtained from Thermo Fisher Scientific (Waltham, MA, USA). Sodium carbonate, sodium nitrate, ethylenediaminetetraacetic acid (EDTA), p-benzoquinone and t-butanol were purchased from Penta (Chrudim, Czech Republic). Distilled water was used for the preparation of solutions and experiments.
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9

Synthesis of Arenediazonium Tosylates

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Chloroauric acid tetrahydrate (HAuCl44 H2O, 99.9 %), silver nitrate (AgNO3, 99.0 %), ascorbic acid (AA, 99.0 %), p‐toluenesulfonic acid monohydrate (98.0 %), acetic acid (≥99.7 %), tert‐butyl nitrite (90.0 %), 4‐nitroaniline (≥99 %), 4‐aminobenzoic acid (≥99 %), 4‐aminoaniline (≥99.0 %), and diethyl ether (≥99.7 %) were purchased from Sigma–Aldrich. All chemical reagents were used as received without further purification. Mueller–Hinton agar (MHA) was prepared as described by the producer (Oxoid, CM0337) and sterilized in an autoclave. Deionized water was used throughout the experiments. The corresponding arenediazonium tosylates (4‐nitrobenzenediazonium tosylate, 4‐aminobenzenediazonium tosylate, and 4‐carboxybenzenediazonium tosylate) were prepared according to the described procedure.55
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10

Synthesis of Organic Compounds via Palladium Catalysis

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All
the chemical precursors,
namely, 4-iodoanisole, 4-nitroaniline, Cu powder, K2CO3, 18-Crown-6, Pd/C (10%), KOH, 1,10-phenanthroline, CuI, and
phenothiazine, as well as the solvents, were purchased form Sigma-Aldrich
and used without further purification. Compound 3 and 4 were synthesized according to previously reported methods.56 (link),57 (link) All the reactions were carried out under an inert environment in
Schleck tube. 1H and 13C NMR spectra were recorded
with 500 MHz JEOL spectrometer in CDCl3 against tetramethylsilane
as reference. Mass spectroscopy was carried out using a high-resolution
ESI-TOF LCT Premier XE mass spectrometer (Waters Corp.). The analyte
was dissolved in chloroform/methanol (c
0.01 mg/mL). More details on the synthesis are in the Supporting Information.
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