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Prepared Polymer (prepared + polymer)
Selected AbstractsPhase Transition Behavior of Novel pH-Sensitive Polyaspartamide Derivatives Grafted with 1-(3-Aminopropyl)imidazoleMACROMOLECULAR BIOSCIENCE, Issue 9 2006Kwangwon Seo Abstract Summary: New pH-sensitive polyaspartamide derivatives were synthesized by grafting 1-(3-aminopropyl)imidazole and/or O -(2-aminoethyl)- O,-methylpoly(ethylene glycol) 5000 on polysuccinimide for application in intracellular drug delivery systems. The DS of 1-(3-aminopropyl)imidazole was adjusted by the feed molar ratio, and the structure of the prepared polymer was confirmed using FT-IR and 1H NMR spectroscopy. Their pH-sensitive properties were characterized by light transmittance measurements, and the particle size and its distribution were investigated by dynamic light scattering measurements at varying pH values. The pH-sensitive phase transition was clearly observed in polymer solutions with a high substitution of 1-(3-aminopropyl)imidazole. The prepared polymers showed a high buffering capacity between pH 5 and 7, and this increased with the DS of 1-(3-aminopropyl)imidazole. The pH dependence of the aggregation and de-aggregation behavior was examined using a fluorescence spectrometer. For MPEG/imidazole- g -polyaspartamides with a DS of 1-(3-aminopropyl)imidazole over 82%, self aggregates associated with the hydrophobic interactions of the unprotonated imidazole groups were observed at pH values above 7, and their mean size was over 200 nm, while the aggregates of polymers were dissociated at pH values below 7 by the protonation of imidazole groups. These pH-sensitive polyaspartamide derivatives are potential basic candidates for intracellular drug delivery carriers triggered by small pH changes. Mean particle size change of MPEG/imidazole- g -polyaspartamide as pH is varied. [source] Electrosynthesis of Poly(para)phenylene in an Ionic Liquid: Cyclic Voltammetry and in Situ STM/Tunnelling Spectroscopy StudiesCHEMPHYSCHEM, Issue 3 2008T. Carstens Abstract The electropolymerization of benzene in the air and water-stable ionic liquid 1-hexyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate (HMIm)FAP is investigated. The study comprises cyclic voltammetry, IR and in situ STM/tunnelling spectroscopy measurements. The IR results indicate that poly(para)phenylene is the end product of the electropolymerization of benzene in the employed ionic liquid. The resulting conjugation lengths of the product fall between 19 and 21. A polymer reference electrode is used successfully for the electrochemical polymerization of benzene. The first in situ STM results show that the electropolymerization of benzene in the ionic liquid can be probed on the nanoscale and the band gap of the prepared polymer can be determined. The electrodeposited polymer film obtained at a constant potential of 1.0 V vs PPP (polyparaphenylene) exhibits a band gap of 2.9±0.2 eV. [source] Functional syndiotactic poly(,-hydroxyalkanoate)s via stereoselective ring-opening copolymerization of rac -,-butyrolactone and rac -allyl-,-butyrolactoneJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2009Noureddine Ajellal Abstract The copolymerization of racemic ,-butyrolactone (rac -BLMe) with racemic "allyl-,-butyrolactone" (rac -BLallyl) in toluene, catalyzed by the discrete amino-alkoxy-bis(phenolate) yttrium-amido complex 1, gave new poly(,-hydroxyalkanoate)s with unsaturated side chains. The poly(BLMe - co -BLallyl) copolymers produced have a highly syndiotactic backbone structure (Pr = 0.80,0.84) with a random enchainment of monomer units, as evidenced by 13C NMR, and high molecular weight (Mn up to 58,000 g mol,1) with a narrow polydispersity (Mw/Mn = 1.07,1.37), as determined by GPC. The comonomer incorporation (5,50 mol % rac -BLallyl) was a linear function of the feed ratio. The pendant vinyl bond of the side-chains in those poly(BLMe - co -BLallyl) copolymers allowed the effective introduction of hydroxy or epoxy groups via dihydroxylation, hydroboration-oxidation or epoxidation reactions. NMR studies indicated that all of these transformations proceed in an essentially quantitative conversion and do not affect the macromolecular architecture. Some thermal properties (Tm, ,Hm, Tg) of the prepared polymers have been also evaluated. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3177,3189, 2009 [source] Synthesis and polymerization reactions of cyclic imino ethers.JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 1 2006Abstract Homopolyaddition reactions of AB-type monomers containing a 2-oxazoline and a phenol group in different positions of the phenyl ring, namely, 2-(4-hydroxyphenyl)-2-oxazoline, 2-(3-hydroxyphenyl)-2-oxazoline, 2-(2-hydroxyphenyl)-2-oxazoline, and 2-(4-hydroxyphenyl)-4,4-dimethyl-2-oxazoline, were studied. Except for 2-(4-hydroxyphenyl)-4,4-dimethyl-2-oxazoline, the reaction carried out in bulk or a solution of highly boiling solvents resulted in the formation of poly(ether amide)s with molecular weights in the range of 103 to 104 as measured by vapor pressure osmometry and gel permeation chromatography. A mechanism of the growth reaction, including a nucleophilic attack of a phenol group to a 2-oxazoline ring in the 5-position, was suggested. The polymerization was accompanied by a side reaction of the amido groups formed by the primary reaction of the 2-oxazoline ring. This led to branching of the main chain. The thermal properties of the prepared polymers were evaluated. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 343,355, 2006 [source] | ||||||||||