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Novel Monomer (novel + monomer)
Selected AbstractsBehaviors of self-assembled diblock copolymer with pendant photosensitive azobenzene segmentsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2010Jui-Hsiang Liu Abstract A novel monomer, ethyl 4-[4-(11-methacryloyloxyundecyloxy)phenyl azobenzoyl-oxyl] benzoate, containing a photoisomerizable NN group was synthesized. The monomer was further diblock copolymerized with methyl methacrylate. Amphiphilic diblock copolymer poly(methyl methacrylate- block -ethyl 4-[4-(11-methacryloyloxyundecyloxy)phenyl azobenzoyl-oxyl] benzoate (PMMA - b - PAzoMA) was synthesized using atom transfer radical polymerization. The reverse micelles with spherical construction were obtained with 2 wt % of the diblock copolymer in a THF/H2O mixture of 1:2. Under alternating UV and visible light illumination, reversible changes in micellar structure between sphere and rod-like particles took place as a result of the reversible E-Z photoisomerization of azobenzene segments in PMMA - b - PAzoMA. Microphase separation of the amphiphilic diblock copolymer in thin films was achieved through thermal and solvent aligning methods. The microphases of the annealed thin films were investigated using atom force microscopy topology and scanning electron microscopy analyses. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1142,1148, 2010 [source] Ring-opening metathesis polymerization of functionalized cyclooctene by a ruthenium-based catalyst in ionic liquidJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2007Huijing Han Abstract This paper describes the synthesis of a novel monomer of 5-substituted cyclooctene with the pendant of imidazolium salt (7) and the ring-opening metathesis polymerization of the functionalized cyclooctenes (4 and 7) in CH2Cl2 and ionic liquid [bmim][PF6] by a ruthenium-based catalyst RuCl2(PCy3)(SIMes)(CHPh) (2). The polymerization, which was carried out in ionic liquid, afforded improved control over the molecular weight (Mn) and polydispersity of the resultant products (PDI <1.4). Furthermore, to facilitate the GPC measurement for molecular weight of polymers, the charged polymers (poly- 7) were hydrolyzed to give uncharged polymers (poly- 4*) by removing the imidazolium pendant from the polymer chains. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3986,3993, 2007 [source] Synthesis and Properties of a Superabsorbent Polymer Prepared by Copolymerization of Sodium Acrylate with Sodium 1-(Acryloyloxy)propan-2-yl PhosphateMACROMOLECULAR REACTION ENGINEERING, Issue 2 2007Zhenbin Chen Abstract A novel monomer, 1-(acryloyloxy)propan-2-yl phosphoryl dichloride, was synthesized and characterized in this work. Thereafter, the monomer was neutralized with sodium hydroxide and copolymerized with sodium acrylate to obtain a superabsorbent polymer. The superabsorbent polymer was then modified to improve its swelling properties (i.e., the water absorbency under load, the hydrogel strength, the resilience and the dispersion). Both single factor and orthogonal design experiments were adopted to obtain optimal conditions. The superabsorbent polymer prepared under the optimal conditions showed improved water absorbency in physiological saline [17 g,·,g,1 under load (P,=,2,×,103 Pa) and 65 g,·,g,1 at atmospheric pressure] and other swelling properties, such as hydrogel strength, resilience and dispersion, also improved. [source] Bioactive polyurethanes in clinical applications,POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 9-10 2006G. Ciardelli Abstract Biomaterials play an important role in most tissue engineering strategies. They can serve as substrates on which cell populations can attach and migrate, can be used as cell delivery vehicles and as bioactive factor carriers to activate specific cellular functions. A series of biodegradable polyurethanes (PUs) with tunable chemical, physical and degradation properties, showing an adequate response to in vitro tests was proposed for applications in soft tissue engineering. Three-dimensional scaffolds of superimposed square meshed grids were prepared by using a rapid prototyping technique (pressure activated microsyringe, PAM) and tested in vivo. Functionalization of PU systems was performed in order to control the chemistry of the materials for the promotion of highly specific binding interactions between materials and biological environments. Two different approaches were used for the coupling of bioactive molecules such as gelatin. The first involved the modification of the polymer chain through a novel monomer and the second one consisted in a surface modification by plasma-induced graft copolymerization of acrylic acid. Copyright © 2006 John Wiley & Sons, Ltd. [source] Selective polymerization of functional monomers with Novozym 435JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 24 2007Martijn A. J. Veld Abstract Two novel monomers, ambrettolide epoxide and isopropyl aleuriteate, encompassing functional groups, were obtained in a single step from commercially available materials. Novozym 435 catalyzed ring opening polymerization of ambrettolide epoxide furnished a polymer of Mn = 9.7 kg/mol and PDI = 1.9 while the epoxide groups remained unaffected during the polymerization. Selective polymerization of the primary hydroxyl groups of isopropyl aleuriteate using Novozym 435 was feasible and a polymer with moderate molecular weight (Mn = 5.6 kg/mol, PDI = 3.2) was isolated in moderate yield (43%). Subsequently, copolymerization of isopropyl aleuriteate with ,-CL in different ratios was performed, resulting in soluble, hydroxy functional polymers with good molecular weights (Mn = 10.4,27.2 kg/mol) in good yield (71,78%). The secondary hydroxy groups in the polymer reacted easily with hexyl isocyanate, showing the potential of isopropyl aleuriteate as a comonomer for the synthesis of functional polyesters. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5968,5978, 2007 [source] Synthesis and polymerization reactions of cyclic imino ethers.POLYMER ENGINEERING & SCIENCE, Issue 8 2007To study the effect of nonequal reactivity of B units in ABx monomers, two novel monomers for synthesis of hyperbranched polymers of the polyaddition type, namely 2-(2,5-dihydroxyphenyl)-2-oxazoline (2a) and 2-(2,4-dihydroxyphenyl)-2-oxazoline (2b) were prepared and characterized. Both monomers have one free phenolic group and one hydrogen-bonded phenolic group with the difference in chemical shift more than 2 ppm. Both monomers undergo thermally initiated polymerization in bulk and in solution at the temperature 220°C during 1 h in bulk and 24 h in solution of 1-chloronaphthalene. Products are white powders with degree of polymerization 17 and 13 for the respective polymer 3a and 3b. The degree of branching is 0.37 and 0.3 for the respective polymer. The structure of polymers is in agreement with the structure, which was expected from the structure of monomers and consists of linear, dendritic, and terminal units. POLYM. ENG. SCI., 47:1272,1280, 2007. © 2007 Society of Plastics Engineers [source] | ||||||||||