Sine functions on compact commutative hypergroups

Recently, Fechner and Székelyhidi introduced sine functions on hypergroups. They conjectured that on a compact hypergroup, all sine functions are constant zero. We prove this conjecture for compact commutative hypergroups by Fourier analysis.     

Oligosaccharide-modified poly(propyleneimine) dendrimers: synthesis, structure determination, and Cu(II) complexation

The multiple application of reductive amination on primary amino groups of first and second generation poly(propyleneimine) dendrimers is used as a one-pot approach to introduce twice the amount of the oligosaccharide units as surface groups, compared to initially present amino groups in the first and second generation dendrimers. This was proven by (1)H NMR, MALDI-TOF-MS, and LILBID-MS analysis. The size of these dendrimers was determined by the hydrodynamic radius using pulsed field gradient NMR and dynamic light scattering. Molecular modeling confirmed the presence of dense-shell dendrimers. These dendrimers exhibit a generation dependent Cu(II)/dendrimer ratio in an aqueous environment, highlighting these materials as possible metal-carrier systems with a well-defined oligosaccharide protection shell for application in a biological environment.     

Novel Hyperbranched Poly([1,2,3]‐triazole)s Derived from AB2 Monomers by a 1,3‐Dipolar Cycloaddition

Summary: Novel hyperbranched poly([1,2,3]‐triazole)s were synthesized from several AB₂ monomers by a 1,3‐dipolar cycloaddition reaction. The compound 3,5‐bis(propargyloxy)benzyl azide was polymerized thermally at room temperature leading to 1,4‐ and 1,5‐disubstituted poly([1,2,3]‐triazole) and catalytically leading only to the 1,4‐disubstituted poly([1,2,3]‐triazole). Only the thermal reaction led to fully soluble products. The AB₂ monomers containing an internal alkyne A unit could be autopolymerized thermally under mild reaction conditions leading to soluble, high‐molecular‐weight hyperbranched poly([1,2,3] triazole)s. All products were characterized by detailed NMR investigations.

Synthesis route for polymers 8a and 8b .     

Three-Dimensional Regularities of Changes of Interelement Influence in Energy-Dispersive X-Ray Fluorescence Analysis

The insufficient energy resolution of detectors is the reason of effect of interelement influence, which reduces a precision in energy-dispersive X-ray fluorescence analysis (XRED) with semi-conductor detectrs and new method of total external reflection (TXRF) which ensures record sensitivity - up to (10^-11-10^-13) g. Taking into account this effect is a necessary stage of existing analysis techniques which tend to ensure identity of composition of sample and standard or use decomposition of a multiple on components on spectra of the monostandards. However, an impossibility to achieve an absolute identity of sample composition as well as fluctuations of the energy resolution result in serious errors and do not allow to analyze and take into consideration the effect of elements not present in composition of the standards.     

Hyperbranched thermolabile polycarbonates derived from a A2+B3 monomer system

Hyperbranched polycarbonates were synthesized successfully via the A₂ + B₃ route by the reaction of a bis(carbonylimidazolide) with triethanolamine. These polymers containing the carbonate group as thermolabile moiety are decomposing into volatile products at around 200°C. The polymers were characterized with ¹H/¹³C NMR spectroscopy, SEC, DSC and TGA techniques.     

Preparation and properties of thin films of hyperbranched polyesters with different end groups

Hyperbranched polyesters (HBP) with different end groups were prepared as thin films. They were characterized with regard to their chemical composition, thickness, optical constants and morphology using infrared spectroscopy, spectroscopic ellipsometry, and atomic force microscopy. The surface properties of the films were determined by zeta‐potential and contact angles measurements. The differences in the molecular structure and surface energetic and acid‐base properties between HBP materials with carboxylic, hydroxy and acetoxy end groups result in differences in their swelling behavior in atmospheric humidity. The swelling behavior at different atmospheric humidity was observed in situ using spectroscopic ellipsometry and reflectometric interference spectroscopy. From the results it can be concluded that HBP films can be used potentially as sensoric materials.     

Synthesis of oxazoline functionalized polypropene using metallocene catalysts

Using two different zirconocene/MAO catalyst systems, propene was copolymerized with the comonomers 2‐(9‐decene‐1‐yl)‐1,3‐oxazoline and 2‐(4‐(10‐undecene‐1‐oxo)phenyl)‐1,3‐oxazoline, respectively. The catalysts used were rac‐Et[Ind]₂ZrCl₂ and rac‐Me₂Si[2‐Me‐4, 5‐BenzInd]₂ZrCl₂. Up to 0.53 mol‐% oxazoline could be incorporated into polypropene. Oxazoline content, molecular weight, degree of isotacticity and melting behavior were dependent on the catalyst system, comonomer structure and comonomer concentration in the feed.     

Synthesis of Dendronized Diblock Copolymers via Click Chemistry: The Effect of Dendronization on Phase Separation Behaviour

A novel route towards the synthesis of well‐defined linear–dendronized diblock copolymers is reported. Precursor alkyne containing diblock copolymers were modified in a highly efficient cycloaddition reaction with dendritic azides of different generation. The dendronization has been shown to be selective and could be driven to completion under ambient conditions. The phase separation of such dendronized diblock copolymers was investigated in dependence of the generation size being attached. Compared to a linear–linear diblock copolymer as starting material the dendronization yielded in a pronounced phase separation. The nanoscaled features observed in thin films strongly depended on the dendron size and a variety of morphologies could be identified. Hence, the unique combination of controlled radical polymerization and click chemistry allows for the triggering of structured surfaces in the nanometer‐regime.

     

The Role of Solvent Ligated Metal Complexes Associated with Weakly Coordinating Counteranions (WCAs) in Isobutylene Polymerization

Summary: Polyisobutylene is an industrially important polymer which is conventionally prepared by polymerization at temperatures below 0 °C. The application of solvent ligated metal complexes associated with weakly coordinating counteranions (WCAs), however, allows the room temperature (30 °C) polymerization of isobutylene resulting in highly reactive polyisobutylene (HR-PIB) containing a high content of terminal double bonds. Recently described complexes include manganese (II), copper(II), molybdenum(III) and zink(II) complexes which were coordinated octahedrally with the boron and alumina based WCAs, each with its own advantages and traits.     

Organic-mineral composites copper oxide/chitosan/carbon fiber obtained by the electrodeposition method

The methods of the coprecipitation of chitosan and copper-containing particles on a carbon fiber used as a cathode and also of the precipitation of copper(II) on a carbon-fiber electrode preliminarily modified by chitosan were studied for feasibility of obtaining composites containing copper oxide/copper in a chitosan matrix. The composition, morphology, structure of the organic-mineral composites were studied by the methods of X-ray phase analysis, scanning electronic microscopy, X-ray photoelectron spectroscopy, and ESR spectroscopy.