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FT-IR spectra of the SBs and polymers

FT-IR spectra of the SBs and polymers

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Polyazomethines containing silane and phosphazene groups were synthesized via elimination reactions of dihydroxy compounds containing imine bonding with phosphazane and silane dichloride. The structures of monomers and polymers containing phosphazane and silane groups were supported by (1)H-NMR, (13)C-NMR, FT-IR and UV-Vis techniques. Electrochemic...

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Two Schiff bases were accomplished through a condensation reaction between salicylaldehyde and ortho-anisidine or para-anisidine. The oxidative polycondensation reaction conditions of 2-[(2-methoxyphenylimino)methyl)phenol (SB1) and 2-[(4-methoxyphenylimino)methyl] phenol (SB2) were determined by H2O2, NaOCl, and air oxidants in an aqueous alkaline medium at different temperatures and reaction times. The % conversion ratios (oligo-2-[(2-methoxyphenylimino)methyl)phenol (oligo-SB1) and oligo-2-[(4-methoxyphenylimino) methyl]phenol (oligo-SB2) were studied in optimum reaction conditions. The structural characterizations of compounds were defined with ¹H- ¹³C-NMR, FT-IR, and size exclusion chromatography (SEC) measurements. Electrochemical and thermal features of compounds were studied by UV-Vis spectroscopy, cyclic voltammetry (CV), FE-SEM, and TG-DTA, respectively. Moreover, conductivity and surface morphologies measurements of oligo-SB1 and oligo-SB2 were carried out by four-point probe technique and FE-SEM, respectively. The conductivity values of the oligo-SB1 and oligo-SB2 were found to be 4.12×10⁻⁶ S cm⁻¹ and 4.87×10⁻⁴ S cm⁻¹, respectively. The residue amounts of oligo-SB1 and oligo-SB2 at 1000°C were found as 45.52% and 55.46%, respectively. Thermal stability, optical properties and conductivity values of oligo-SB2 were better than oligo-SB1.