Search results for " POLYMER"

Characterization of sulfobetaine monomers by nuclear magnetic resonance spectroscopy: a note

1995

A set of zwitterionic monomers bearing the 3-ammoniopropanesulfonate moiety is analysed in CDCl3, CD3OD and D2O by one- and two-dimensional H-1 n.m.r. and C-13 n.m.r. spectroscopy. Absolute and relative positions of the n.m.r, signals are determined depending on the solvent used; the refined assignments of the signals in the vicinity of the ammonium group deviate from previously proposed assignments based on standard n.m.r, shift tables. Still, there is no convincing evidence for a special ring current effect due to a six-membered ring conformation of the betaine moiety.

Synthesis and characterization of bi-functional photorefractive polymers

2001

Abstract A novel bi-functional photorefractive acrylate polymer with pendant carbazolyl groups and azo derivatives as side chains was synthesized, in which azo derivatives as electro-optic chromophores and carbazolyl as photoconductive moiety were covalently linked on the acrylate backbone. Photorefractive experiments showed that a high two-beam coupling gain coefficient of 93 cm −1 , diffraction efficiency of 12% and electro-optic coefficient of 26 pm/V were obtained. With increasing writing beam's intensity, the two-beam coupling enhanced gradually, and then reached saturation. Using the method of four-wave mixing, the photoisomerization grating was observed.

Darstellung und polymerisation von diestern aus 2,2′-methylendiphenolen und acryl-, methacryl- bzw. Crotonsäure

1984

Several mono- and diesters of four selected 2,2′-methylenediphenols with acrylic, methacrylic, and crotonic acid were synthesized for the first time. Special emphasis was paid to the preparation of diesters with two different acyl groups which could be obtained via the corresponding monoesters. The radical polymerization of these esters with AIBN (mainly in benzene) gave insoluble (crosslinked) products from dimethacrylates and soluble (linear) polymers from mixed diesters with methacrylic and crotonic acid, while the dicrotonates are not reactive.

Polymerizable and polymeric zwitterionic surfactants: 2. Surface activity and aggregation behaviour in aqueous systems

1991

Abstract The surfactant properties of a series of permanently zwitterionic monomers and polymers were studied with respect to structural variations. A strong influence of the molecular geometry on solubility and aggregation behaviour was observed, in particular for the polymers. Whereas all monomers were water-soluble and true surfactants, the water solubility of the polymers was restricted to selected geometries. Water-soluble polymers showed the properties of classical polysoaps, i.e. low surface activity and solubilization power for hydrophobic solutes. In contrast, water-insoluble polymers formed stable monolayers at the air-water interface and could be deposited onto solid substrates b…

Amphotropic Ionomers by Attachment of Secondary Amines to a Reactive Ester Polymer

2004

We report on the synthesis of polyacrylamides that were prepared by the reaction of a reactive ester polymer with a mesogen-containing secondary amine and N-methyl-piperazine. As the polymers do not form hydrogen bonds near the amide groups, their mobility is significantly higher than that of poly(N-monoalkylacrylamides). The initially nonionic polymer shows no liquid-crystalline behavior in bulk and in mixture with ethylene glycol. This is due to the low polarity difference between the different side chains. The polarity difference can be increased by protonation or quarter-nization of the tertiary amino groups, and liquid-crystalline behavior is observed. The self-assembly multilayer buil…

1985

Etude de polyesters avec du triphenylene ou du benzene comme cœur du discogene et des espaces flexibles alkylene

1992

A series of liquid-crystalline copolymers 1 with a chiral azobenzene moiety as photoreactive mesogenic unit was prepared. The polymers were fractionated and the mesophase behaviour of the high- and low-molecular weight fractions was examined. The copolymers display smectic A and cholesteric phases. For the cholesteric phases the pitch of the helix was determined, which ranges from 3 to 20 μm. Stable monolayers at the air-water interface were obtained from two monomers and one of the homopolymers. Multilayer assemblies of the azobenzene-containing polymers can be used to study photo-induced order/disorder transitions.

Controlled synthesis of poly(acetone oxime acrylate) as a new reactive polymer: Stimuli-responsive reactive copolymers

2007

Abstract Acetone oxime acrylate has been synthesized as a new active ester monomer. Free radical polymerization yielded a reactive polymer soluble in various organic solvents, such as chloroform, dioxane, DMSO, acetone, methanol, dichloromethane, DMF, and ethanol. Controlled radical polymerization of acetone oxime acrylate was successfully conducted using the RAFT, NMP and Iniferter method. Partly polymer analogous reaction with N-isopropylamine resulted in the reactive copolymer poly(N-isopropylacrylamide-co-acetone oxime acrylate), which featured a lower critical solution temperature (LCST) of 61 °C in water. Further, the reactivity of the copolymer was exemplary proven by complete reacti…

Interfacial stabilization by soft Janus nanoparticles

2016

Abstract The stabilization of water/air, water/oil and water/solid interfaces by Janus particles with polystyrene (PS) and poly(methacrylic acid) (PMAA) hemispheres was systematically investigated. The stabilization of these interfaces is of relevance for the formulation of foams, emulsions and dispersions. The Janus particles were prepared from micellar solutions of polystyrene-b-polyisoprene-b-poly(tert-butyl methacrylate) (PS-PI-PtBMA) triblock terpolymers by selective cross-linking of the polyisoprene domain on a multi-gram scale, followed by hydrolysis of the PtBMA block. For the investigation of water/oil-emulsions a series of hydrophobic oils (paraffin oil, xylene, peanut oil, isopro…

Mechanism of Anionic Polymerization of (Meth)acrylates in the Presence of Aluminum Alkyls, 6. Polymerization of Primary and Tertiary Acrylates

1998

The kinetics of the polymerization of n-butyl acrylate initiated by lithiated ester enolates in the presence of aluminum alkyls was investigated in toluene and in toluene/Lewis base mixed solvents at −78 °C. In pure toluene, curved time−conversion plots, incomplete monomer conversion, and broad molecular weight distributions (Mw/Mn ≈ 2) are observedin the absence of aluminum alkyls the molecular weight distributions are significantly broader (Mw/Mn > 14). High monomer conversions and narrower molecular weight distributions (Mw/Mn ≈ 1.5) are obtained when using Lewis bases (e.g., methyl pivalate) as cosolvents. The polymerization of tert-butyl acrylate rapidly reaches full monomer conversion…