Abstract:Chemical modification of inexpensive commercial polymers, such as styrene, is a safe methodology to obtain new copolymers. The 4-chloromethyl styrene (CMS) was copolymerized with styrene (in various mole ratios) by free radical polymerization method at 70 ºC using α,α-azobis(isobutyronitrile) (AIBN) as an initiator. The azide ion was covalently attached to the obtained copolymers with replacement of all the chlorine atoms in CMS units. The 1,3-dipolar click cycloaddition reaction between azido polymers and dim… Show more
“…As shown in Scheme 3, GATA was deprotected using a catalytic quantity of sodium methoxide in methanol [13]. The FT-IR spectrum shows the complete Odeacetylation.…”
Section: Resultsmentioning
confidence: 99%
“…Cubane-1,4-bis (methacryloyloxyethyl) carboxylate (CA), glucose-6-acrylate-1,2, 3,4-tetraacetate (GATA) and glucose-6-acrylate (GA) were prepared using the methods described in the literature [11][12][13]. Estradiol was purchased from SigmaAldrich.…”
For the first time, the glucose-6-acrylate-1,2,3,4-tetraacetate (GATA) monomer was prepared under mild conditions. The removal of protecting acetate groups from GATA was carried out before the silylation and then Me 3 Si was covalently linked with glucose acrylate (GA). Cubane-1,4-dicarboxylic acid (CDA) was covalently linked with 2-hydroxyethyl methacrylate (HEMA). The silyl-linked GA is abbreviated as TMSiGA. CDA linked to two HEMA groups was used as the cross-linking agent (CA). Free radical crosslinking co-polymerization of the methacrylic acid (MAA) and hydrophobic glycomonomer (TMSiGA) with two different molar ratios of CA was carried out at 60-70 • C. The compositions of the cross-linked threedimensional polymers were determined by FT-IR spectroscopy. A model hydrophobic drug, the steroid hormone estradiol, was entrapped in these gels and the in vitro release profiles were carried out in enzymefree simulated gastric and intestinal fluids (SGF and SIF, respectively). To overcome the hydrophobicity of estradiol, the buffers for estradiol were modified by adding ethanol. The influence of the structures and amounts of silane monomers on the swelling and drug-release behaviors were studied.
“…As shown in Scheme 3, GATA was deprotected using a catalytic quantity of sodium methoxide in methanol [13]. The FT-IR spectrum shows the complete Odeacetylation.…”
Section: Resultsmentioning
confidence: 99%
“…Cubane-1,4-bis (methacryloyloxyethyl) carboxylate (CA), glucose-6-acrylate-1,2, 3,4-tetraacetate (GATA) and glucose-6-acrylate (GA) were prepared using the methods described in the literature [11][12][13]. Estradiol was purchased from SigmaAldrich.…”
For the first time, the glucose-6-acrylate-1,2,3,4-tetraacetate (GATA) monomer was prepared under mild conditions. The removal of protecting acetate groups from GATA was carried out before the silylation and then Me 3 Si was covalently linked with glucose acrylate (GA). Cubane-1,4-dicarboxylic acid (CDA) was covalently linked with 2-hydroxyethyl methacrylate (HEMA). The silyl-linked GA is abbreviated as TMSiGA. CDA linked to two HEMA groups was used as the cross-linking agent (CA). Free radical crosslinking co-polymerization of the methacrylic acid (MAA) and hydrophobic glycomonomer (TMSiGA) with two different molar ratios of CA was carried out at 60-70 • C. The compositions of the cross-linked threedimensional polymers were determined by FT-IR spectroscopy. A model hydrophobic drug, the steroid hormone estradiol, was entrapped in these gels and the in vitro release profiles were carried out in enzymefree simulated gastric and intestinal fluids (SGF and SIF, respectively). To overcome the hydrophobicity of estradiol, the buffers for estradiol were modified by adding ethanol. The influence of the structures and amounts of silane monomers on the swelling and drug-release behaviors were studied.
“…Azaheterocycles are obviously suitable scaffolds for achieving nitrogen-rich polymers. There is a considerable interest in polyvinyltetrazoles (PVT) containing a large amount of nitrogen because of their powerful energetics, [1][2][3] interpolymer complexity, [4,5] biological activity, high thermostability, [6][7][8] and good solubility in various solvents, [9] exhibiting wide applications including dynamite, polyelectrolytes, [10,11] distinctive complex, [12] biocompatible material of different natures, and oxygen enriching membrane. [13][14][15] The investigation on the radical (co)polymerization, [16] radiation-induced bulk polymerization, [17] solution interdiffusion, [18,19] solution properties and kinetics of solution formation in various media, [20] rheological properties, [21] swelling thermodynamics, [22] and thermal degradation and its kinetics and mechanism of the PVT has been reported.…”
The novel functionality of aromatic tetrazole derivatives with high nitrogen content predetermines a great interest to tetrazole-containing polymers. Poly(5-vinyltetrazole) is one of the most attractive polymers containing tetrazoles. The 4-chloromethyl styrene (CMS) was copolymerized with acrylonitrile (in various mole ratios) by free radical polymerization method at 70°C using α,α-azobis(isobutyronitrile) as an initiator. The reaction azide ion with copolymers, simultaneously with replacement of all the chlorine atoms in CMS units, causes the nitrile groups are entirely converted to tetrazole in dimethylformamide at elevated temperatures. The polymers, obtained in quantitative yields, were characterized by FT-IR and 1 H NMR spectroscopy, differential scanning calorimetry, and gel permeation chromatograph studies. Thermal properties nitrogen-rich polymers show that explosive thermal degradation takes place at around 260°C.
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