The monomer phenyl acrylamide was synthesized by reacting acrylamide with chloro benzene in the presence of pyridine. Copolymer of phenyl acrylamide (PAM) with methyl methacrylate (MMA) was synthesized by free radical technique using dimethylsulfoxide (DMSO) as solvent and benzoyl peroxide (BPO) as initiator. The overall conversion was kept low (≤ 15% wt/wt) for all studies copolymers samples. The synthesized copolymers were characterized using fourier transform infrared spectroscopy (FT-IR), and their thermal properties were studied by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The copolymers compositions were determined by elemental analysis. The monomer reactivity ratios have been calculated by linearization methods proposed by Kelen-Tudos and Fineman-Ross. The derived reactivity ratios (r1, r2) for (PAM-co-MMA) are: (0.03, 0.593). The microstructure of copolymers and sequence distribution of monomers in the copolymers were calculated by statistical method based on the average reactivity ratios and found that these values are in agreement with the derived reactivity ratios. Copolymers of PAM with MMA formed alternating copolymers.
New tridentate ligand 1-(2, 2-dicyclohexylethyl)-3-(1, 5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-ylimino)indolin-2-one (L) was synthesized from the reaction of 3-(1,5-dimethyl-3oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-ylimino)indolin-2-one and dicyclohexyl amine. Monomeric complexes of this ligand, of general formulae [VO II (L)(SO4)], [M III (L)Cl3] with M=Cr III and Fe III , and [M II (L)Cl]Clwith (M = Mn II and Co II) are reported. The mode of bonding and overall geometry of the complexes were determined through FT-IR, UV-Vis, and mass spectral studies, magnetic moment measurements, elemental analysis, metal content, chloride containing and molar conductance. These studies revealed octahedral geometries for the Fe III , Cr III complexes, square pyramidal for VO (II) complex and tetrahedral for the Mn II and Co II complexes. The study of complexes formation via molar ratio and job method in DMF solution has been investigated and results were consistent to those found in the solid complexes with a ratio of (M:L) as (1:1). Hyper Chem-8 program has been used to predict structural geometries of compounds in gas phase the heat of formation (ΔHf º), binding energy (ΔEb), total energy, electronic energy and dipole moment at 298 o k.
The present work involved synthesis of several new N-Sulfamethoxazol derivatives imide on Polymeric chain by two steps. The first stip involved preparation of N- (sub.orunsub benzoyl and sub unsub acetyl) amidyl sub sulfamethoxazole (1-5) by condensation of sulfamethoxazole drug with many substituted acid chloride, then the second step include, preparation new five N-(acrly-N–sub or unsub benzoyl) imidyl substituted sulfamethoxazol(6-10) by reaction of poly acryloyl chloride with the prepared compound (1-5) in first stepin asuitable solvent in the presenceamount triethylamine (Et3N) with heating. The structure confirmations of all polymers wereconfirmed using FT-IR,1H-NMR,13C-NMR and UV spectroscopy. Other physical properties including softeningpoint's, melting point, and solubility of the polymers were also measured.
This study in volved synthesis of the chelating phenolic polymers functionalized by Mannich base functional groups. The work included two parts ; part one syntheses of Mannich bases monomers formed by the condensation reaction of P-hydroxy benzaldehyde with different secondary amines and Primary amine (Metoclopramide hydrochloride) have been synthesized. Then part two included synthesis of phenolic chelating polymers containing Mannich bases by condensation Mannich bases which prepared in part one with P-hydroxy benzaldehyde and phenol. These chelating polymers were characterized through (FT-IR) and( 1 H-NMR) spectroscopy so measured the thermal stability and study the biological activity of some of the synthesized compounds .
The purpose of this study is to determine the useful of Schiff bases derivatives containing (oxazepine, tetrazole) rings with biological activity which can be used as drug and antimicrobial, the present work is started from [Binary (2,5(4,'4-diaminophenyl) -1,3,4oxadiazole]. A variety of Schiff bases and heterocyclic (oxazepine, tetrazole) have been synthesis, and confirm that structures by physical properties , FTIR , 1H-NMR, 13C-NMR, elemental analysis, [Microbial study against three type of bacteria (staphylococcus aurea and klebsiella pneumonia) and (Canadida albncans) fungi].All analyzation performed in center of consulatation University of Jordan.
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