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5 protocols using salicylaldehyde

1

Synthesis of Zeolite Y Catalysts

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Pure zeolite Y is purchased
from Sigma-Aldrich, India. Salicylaldehyde and its derivatives and
ethylenediamine are purchased from Alfa Aesar, and palladium acetate
is purchased from TCI chemicals, India. All solvents (ethanol, acetone,
methanol, and diethyl ether) are purchased from S.D. Fine, India.
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2

Optimization and Characterization of Novel Compounds

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Ethyl acetoacetate, DPPH, ABTS, deuterated dimethyl sulfoxide, and salicylaldehyde and its hydroxylated derivatives were purchased from Alfa Aesar (Kandel, Germany). Absolute ethanol, piperidine, deuterated chloroform, thiosemicarbazide, and acetic acid were purchased from Merck (Milan, Italy). Reagents were used as received without further purification.
NMR spectra were acquired with a Bruker Advance III HD 600 spectrometer (Rheinstetten, Germany) at room temperature with tetramethylsilane (TMS) as the internal standard in DMSO-d6 or CDCl3. ESI mass spectra were recorded with a triple quadrupole QqQ Varian 310-MS mass spectrometer (Palo Alto, CA, USA) using previously optimized parameters [5 (link)]. High-resolution ESI mass spectra were acquired on a Thermofisher ORBITRAP-ELITE (Waltham, MA, USA). Melting points were measured on a Kofler Hot Stage (Rochford, UK) and are uncorrected.
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3

Synthesis of N-Hexyl Salicylaldimine

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Salicylaldehyde (SA), n-hexylamine (Hex-NH2), ethanol, sodium hydroxide (NaOH), anhydrous sodium sulfate, formaldehyde, 1,4-dioxane (DO), chloroform, sodium borohydride (NaBH4) and dilute hydrochloric acid were purchased from Acros. All melting points were recorded and corrected on the Melt-Temp II melting point instrument. The chemicals and solvents used in this experiment were all purchased from Sigma-Aldrich and are all of the analytical grades.
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4

Metal-Organic Synthesis Protocol

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Chemicals and solvents used in the current work were obtained in their purest forms from different local suppliers like Metal(II) acetates (where metal(II) = Co, Ni, Cu and Zn) from Riedel-de-Haen, Salicylaldehyde from Acros Organics, solvents from Merck and Sigma Aldrich. Metal salts were dried in a vacuum oven for 3–4 h at 80–100 °C before reaction. 2-aminobenzohydrazine was prepared using the previously reported procedure. The reaction environment was kept inert, and the manipulations were carried out in Schlenk line.
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5

Synthesis of Organometallic Compounds and Polymers

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Argon (grade 5.0, Linde Gas), Ti(OiPr)4 (99.999%, Sigma-Aldrich, St. Louis, MO, USA), VO(OiPr)3 (TCI), NaBH4 (98%, Sigma-Aldrich), 2-aminobenzyl alcohol (98%, Sigma-Aldrich), and salicylaldehyde (99%, Acros Organic, Geel, Belgium) were used as received. CDCl3 (99.5 atom % D, Deutero GmbH, Kastellaun, Germany, 99.8 atom % D, 0.03% TMS), CH2Cl2 (Chempur, Piekary Śląskie, Poland, analytical grade), and ε-caprolactone (99%, Alfa Aesar, Haverhill, MA, USA) were dried over molecular sieves. Rac-lactide (99%, Acros Organic, Geel, Belgium) and L-lactide (99%, Aldrich) were purified by vacuum sublimation at 85°C. Hexane (Linegal Chemicals, Blizne Łaszczyńskiego, Poland) and toluene (FP, AnalaR NORMAPUR, VWR, Radnor, PA, USA) were refluxed over sodium and sodium/benzophenone, respectively, and distilled under a nitrogen atmosphere prior to use.
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