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5 protocols using 3 nitrobenzaldehyde

1

Photosensitizer Synthesis and Characterization

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Anthracene, oleic acid, linoleic acid, acetonitrile, methylene blue (MB), DABCO, BHT, BHA, TBHQ, 2-nitrobenzaldehyde, 3-nitrobenzaldehyde, and 4-nitrobenzaldehyde were purchased from Merck or Sigma-Aldrich (Vienna, Austria) and Alfa Aesar (Karlsruhe, Germany) without further purification. 5,10,15,20-Tetrakis(tolyl)porphyrin (H2TTP) and its ferric complex TTPFeCl were synthesized according to the literature [13 (link),14 (link)].
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2

Synthesis of Organotin(IV) Complexes

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2-Hydroxy benzaldehyde, 3-hydroxy benzaldehyde, 4-hydroxy benzaldehyde, 2-nitro benzaldehyde, 3-nitro benzaldehyde, 4-nitro benzaldehyde, 2-hydroxy, 3-methoxy benzaldehyde, 4-hydroxy, 3-methoxy benzaldehyde, malonic acid, ammonium acetate, acetyl chloride, dibutyltin(iv) oxide, dibutyltin(iv) dichloride, tributyltin(iv) chloride, triphenyltin(iv) chloride and tricyclohexyltin(iv) chloride were purchased from Merck Company (Germany). Melting points were determined by Fisher-Johns melting point apparatus (USA) and were found uncorrected. An Eager 300 mass analyzer (USA) was used for elemental analyses. A Bruker FTIR (USA) spectrophotometer TENSOR27 (ZnSe) was used to record the FTIR spectra of the pure solid samples covering 4000–400 cm−1. EI-MS spectra were observed in terms of % m/z on a Finnigan MAT 312 spectrometer (USA). 1H, 13C and 119Sn NMR spectra were calculated with a Bruker AM 400 NMR spectrometer (USA).
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3

Inhibition of α-Glucosidase Activity

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5-chlorosalisaldehyde, 4-N,N-dimethylaminobenzaldehyde, 2-thiophencarboxyaldehyde, 3-nitrobenzaldehyde, cinnamaldehyde, acarbose, potassium Iodide (KI), iodine (I2), potassium dihydrogen phosphate, dipotassium hydrogen phosphate were obtained from Sigma Aldrich (Hamburg, Germany), p-nitrophenyl β-d-glucopyranoside (p-NPG), α-glucosidase, methanol from Merck (KGaA, Darmstadt, Germany), starch, NaHCO3, hydrochloric acid (HCl), glacial acetic acid, absolute ethanol and dimethylsulfoxide (DMSO) from Sigma Aldrich (St. Louis, MO, USA).
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4

Analytical Ranking of Chemicals

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The chemicals of analytical ranking for example 2-Nitrobenzaldehyde, 3-Nitrobenzaldehyde, 4-Nitrobenzaldehyde, 4-Methyl-benzenesulfonylhydrazine, AgNO3, AuCl3, CdSO4, Co(NO3)2, Cr(NO3)3, HgCl2, NiCl2, Y(NO3)3, ZnSO4, EtOH, MeOH, NaH2PO4, Na2HPO4, and nafion (5% ethanolic solution) were purchased from the Sigma Aldrich company, and used as received. A mother solution of Y3+ (100.0 mM) was prepared from the purchased chemical, Y(NO3)3. A Stuart scientific SMP3 (version 5.0) melting point apparatus (Bibby Scientific Limited, Staffordshire, UK) was used to record the melting point (m.p.), and the reported m.p. was not corrected. 1H-NMR, and 13C-NMR spectra were recorded on an AVANCE-III instrument (400 MHz, Bruker, Fallanden, Switzerland) at 300 k, and chemical shifts were reported in ppm with reference with residual solvent signal. FTIR spectra were recorded as neat on a Thermo scientific NICOLET iS50 FTIR spectrometer (Madison, WI, USA). UV-V is study was conducted using Evolution 300 UV-Vis spectrophotometer (Thermo scientific). I-V method was carried out in order to detect Y3+ at a selective point using the modified 2-MNBBSH/GCE by Keithley electrometer (6517A, USA). Warning! Yttrium is poisonous. So, a minute amount of this chemical can be used for the preparation of the essential solution with care.
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5

Synthesis of Organic Compounds

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All the chemicals were obtained from commercial suppliers and were used without further purification. Lead iodide (99.99%, PbI2) and iodine (≥99.99%, I2) were purchased from Alfa Aesar. N,N-Dimethyl formamide (DMF) and hydroiodic acid (55% w/w, HI) were purchased from Fisher Scientific. Benzaldehyde, 2-methoxyBenzaldehyde, 4-chloroBenzaldehyde, 4-bromoBenzaldehyde, 3-nitroBenzaldehyde, cinnamaldehyde, 2-methoxycinnamaldehyde, salicylaldehyde, 2-nitrocinnamaldehyde, benzophenone, and methylamine solution (33 wt% in ethanol) were purchased from Sigma-Aldrich.
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