Partialsynthetische Aristolochiasäuren und Analoge. 3. Mitt.: 3,4,6-Trimethoxy-7-ethoxy- und 3,7-Diethoxy-4,6-dimethoxy-10-nitrophenanthren-1-carbonsäuren

Two further aporphine alcaloids, N-methyllaurotetanine and boldine, were used to the synthesis of aristolochic acid analogs. By means of their destruction and nitration of the reaction products two new nitrophenanthrene acids were obtained and their chemical structures were proved.

     

RCM-based synthesis of a variety of beta-C-glycosides and their in vitro anti-solid tumor activity

The synthesis of a number of biologically relevant C-glycosides has been carried out through the use of an esterification-ring-closing metathesis (RCM) strategy. The required acid precursors were readily prepared via a number of standard chemical transformations followed by dehydrative coupling of these acids with several olefin alcohols 1 to yield the precursor esters 3 in excellent yield. Methylenation of the esters 3 was followed by RCM and in situ hydroboration-oxidation of the formed glycals to furnish the protected beta-C-glycosides 6 in good overall yield. Several examples were converted to the corresponding C-glycoglycerolipids 17 and subsequently screened against solid-tumor cell lines for in vitro differential cytotoxicity.     

Photodegradation studies of novel biodegradable blends based on poly(ethylene oxide) and pectin

Blends of two biodegradable polymers: natural pectin and synthetic poly(ethylene oxide) at different weight-ratios were obtained by physical mixing in aqueous solutions, and evaporation of the solvent. The macromolecular order in the composites was investigated by applying X-ray diffraction, while the surface morphology was observed using atomic force microscopy. The photooxidative degradation of the blends was studied by viscometry, FTIR spectroscopy and UV-vis spectroscopy. It has been found that the susceptibility of the studied composites to UV radiation depends on an appropriate ratio of components, and the most sensitive to UV-irradiation among the samples studied was the equal weight-ratio blend of poly(ethylene oxide)/pectin.     

Preparation and characterization of a proficiency test material “Polish mushrooms” supported by the International Atomic Energy Agency (IAEA), Vienna

Mushroom reference material has been prepared and characterized for use in proficiency test exercises within the frame of an IAEA Interregional Technical Cooperation Project. Laboratories from 14 countries provided results for homogeneity testing and the assignment of property values. The contents of 11 elements have been assigned. The material was used for conducting a proficiency test in Poland and the results obtained by Polish laboratories are presented and discussed.     

Synthesis of porphyrinyl-nucleosides

Several porphyrinyl-nucleosides were prepared in the reaction of the OH group of one, two or four meso-p-hydroxyphenyl substituents of porphyrin with 5′-O-tosylates of 2′,3′-O-isopropylidene-adenosine or -uridine, or 5′-O-tosylthymidine; the remaining porphyrin meso-substituents were p-tolyl, p-hydroxyphenyl or 4-pyridyl. The following porphyrinyl-nucleosides were obtained with 8–17% yield: meso-di(p-tolyl)di(p-phenylene-5′-O-2′,3′-O-isopropylidene-adenosine) (or -uridine)porphyrins 1,2 , the respective meso-tetranucleosideporphyrins 3,4 -meso-mono(p-phenylene-5′-O-thymidine)porphyrins 5–7 , meso-di(p-tolyl)di(p-phenylene-5′-O-thymidine)porphyrins 8,9 and the meso-di(p-hydroxyphenyl)di(p-phenylene-5′-O-thymidine)porphyrins 10. Other compounds prepared belonged to the series: meso(4-pyridyl)_4?n(p-phenylene-5′-O-2′,3′-O-isopropylideneuridine)_nporphyrin, n = 1, 2 or 4, 11–13. N-Methylation gave the water soluble iodide salts: (N-methyl-4-pyridinium)4_4?n(p-phenylene-5′-O-2′,3′-isopropylideneuridine)_nporphyrins, n = 1, 2 or 4, 14–16. The ms fab showed in most cases stepwise detachment of the CH₂(5′)-nucleoside fragments. The porphyrins meso disubstituted by thymidine represent a convenient substrate for the build-up of both nucleoside units into the oligo/polynucleotide chains.     

Solventless transesterification of methyl methacrylate with ethylene glycol. A kinetic approach

The kinetics of solventless transesterification of methyl methacrylate with ethylene glycol has been studied to establish the optimal conditions for ethylene glycol monomethacrylate synthesis. The kinetic data presented show strong dependence of kinetic parameters on initial reagents ratio.

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Surface morphology dependent photoluminescence from colloidal silicon nanocrystals

Monodisperse 1-2 nm silicon nanocrystals are synthesized in reverse micelles and have their surfaces capped with either allylamine or 1-heptene to produce either hydrophilic or hydrophobic silicon nanocrystals. Optical characterization (absorption, PL, and time-resolved PL) is performed on colloidal solutions with the two types of surface-capped silicon nanocrystals with identical size distributions. Direct evidence is obtained for the modification of the optical properties of silicon nanocrystals by the surface-capping molecule. The two different surface-capped silicon nanocrystals show remarkably different optical properties.     

Symmetry and the generation and measurement of optical torque

A key element in the generation of optical torque in optical traps, which occurs when electromagnetic angular momentum is transferred from the trapping beam to the trapped particle by scattering, is the symmetries of the scattering particle and the trapping beam. We discuss the effect of such symmetries on the generation and measurement of optical torque in optical tweezers, and some consequent general principles for the design of optically driven micromachines.