Synthesis Characterization And Photopolymerization Of Novel Phosphonated Materials

New phosphonated cross-linked materials were synthesized from telomers obtained by reaction between 10-undecenol and dialkyl hydrogenphosphonates. Telomers were then converted to materials resins by methacrylation reactions. Finally, photopolymerization of the different materials synthesized was achieved and influence of the nature of the phosphonate group (diester, monoacid and diacid) was also evaluated.New phosphonated cross-linked materials were synthesized from telomers obtained by reaction between 10-undecenol and dialkyl hydrogenphosphonates. Telomers were then converted to materials resins by methacrylation reactions. Finally, photopolymerization of the different materials synthesized was achieved and influence of the nature of the phosphonate group (diester, monoacid and diacid) was also evaluated

Study of the inhibition of corrosion of mild steel in a 1M HCl solution by a new quaternary ammonium surfactant

The anticorrosive effect of surfactant, 12-(2,3-dioxoindolin-1-yl)-N,N,N-trimethyldodecanammonium bromide 3 on the corrosion of mild steel in 1M hydrochloric acid was assessed by gravimetric and electrochemical techniques (potentiodynamic polarization and electrochemical impedance spectroscopy). The results have shown that our synthesized surfactant is an excellent corrosion inhibitor for mild steel in 1 M HCl. Inhibitory efficacy of up to 95.9% was exhibited by surfactant 3 at a concentration of 1 mM after 6 h immersion at 298K. Based on the polarization curves, it is clear that the surfactant 3 can be considered as a mixed inhibitor with a predominantly anodic character. The inhibitory effectiveness increases with increasing concentration but decreases with increasing temperature. It was found that the adsorption of the inhibitor on the surface of the mild steel in 1M HCl followed the Langmuir adsorption isotherm. In this context, the main kinetic and thermodynamic parameters were determined and discussed

SYNTHESIS OF NEW 5-BROMO-1H-INDOLE-2,3-DIONE DERIVATIVES BY 1,3-DIPOLAR CYCLOADDITION

To contribute to the development of the chemistry of 5-bromo-isatin, we have synthesized new heterocyclic systems, using alkylation reactions under conditions of phase transfer catalysis to be then subjected to cycloaddition reactions dipolar involving 1,3-dipoles. The structures of the various products obtained were determined by 1H NMR, 13C NMR spectroscopy