Eine neuc Umlagerung an einem Metathebainon-Derivat mit Cyclohexa-2,5-dienon-Struktur

Zusammenfassung 4-O-Methyl-7,8-dehydro-metathebainon-methin (1) geht in alkalischer Lösung in das Naphthalin-Derivat3 über, das unter Abspaltung von Formiat7 liefert. Das Auftreten von3 kann durch Isolierung von13a nach Reduktion mit NaBH₄ nachgewiesen werden. Die aus3 und7 durch Reduktion erhaltenen Alkohole8a und13a werden in saurer Lösung unter Methanol-Abspaltung zu den 2,3-Dihydro-naphtho[1,8-bc]pyranen9 und14 cyclisiert.

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A new rearrangement of a metathebainone derivative with a cyclohexa-2,5-dienone groupment

4-O-Methyl-7.8-dehydrometathebainonemethine (1) in alkaline solution rearranges to the naphthalene derivative3, which eliminates formiate to give7. The occurrence of3 was confirmed by isolation of13a after reduction with NaBH₄. The hydroxy compounds8a and13a, obtained by reduction, eliminate methanol and cyclize to the 2.3-dihydronaphtho[1.8-bc]pyrans9 and14.

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Mit 2 Abbildungen     

Quantitation of chlordiazepoxide and its metabolites in biological fluids by thin-layer chromatography.

Chlordiazepoxide and its 4 major metabolites were assayed after separation by thin-layer chromatography following extraction from biological fluids. The compounds become intensely fluorescent in the presence of red, fuming nitric acid. The resulting compounds are quantitated with a spectrodensitometer with a fluorescent attachment. The sensitivity varies between 0.05 and 0.1 microgram. The coefficient of variation is 1.4% for assays in urine and 6.4% in serum.     

Total synthesis of the marine alkaloid (-)-lepadin B

An enantioselective total synthesis of (-)-lepadin B has been developed starting from (2S,4S)-2,4-O-benzylidene-2, 4-dihydroxybutanal. The key steps in the synthesis include the use of an aqueous intramolecular acylnitroso Diels-Alder reaction to afford the trans-1,2-oxazinolactam and Suzuki cross-coupling reaction to elaborate the (E,E)-octadienyl unit.     

Reactions of 1-Allenylpyrazole and 1-Allenyl-1,2,4-triazole with Hydrogen Chloride and Metal Chlorides

1-Allenylpyrazole and 1-allenyl-1,2,4-triazole react with hydrogen chloride via proton addition at the pyridine-like nitrogen atom (N² and N⁴, respectively). In the reaction with 1-allenylpyrazole, 1-[(E)-3-chloro-1-propenyl]pyrazole is also formed via regio- and stereoselective addition of hydrogen chloride to the propadienyl group. 1-Allenylpyrazole and 1-allenyl-1,2,4-triazole act as unidentate ligands with respect to Co, Ni, Cu, Zn, Cd, Pd, and Sn, the donor centers being N² and N⁴, respectively. Apart from mononuclear coordination compounds, 1-allenylpyrazole gives rise to polymeric complexes which contain units and blocks formed by the free ligand.     

Atomic spectroscopy for detection in thermal analysis

An atomic absorption spectrophotometer is coupled to a conventional thermoanalytical quartz furnace as used for TG and DTG to detect the thermally evolved products. In this combined system, the dry aerosol (smoke) obtained by cooling the vapour evolved is transported from the furnace to the flame for metal-specific atomic absorption detection. The particular design of the furnace outlet promotes the formation of stable aerosols. Optimum experimental conditions were determined, using zinc chloride solution, by varying the specimen mass, the heating rate and the flow rate of the furnace gas at a linear temperature program. The absorbancevs. temperature curves obtained with this method for various zinc compounds are compared with the corresponding DTG curves. The applicability of the technique for studying heterogeneous reactions with carbon tetrachloride and hexane vapours is presented. The utilization of an atomic absorption spectrophotometer equipped with a quartz cuvette for detecting the thermal evolution of mercury vapours is described, as well as detection potentials by molecular absorption (for NO and NH₃) and light scattering (for smoke evolved from organic matter). The results obtained with the suggested methods may, in some respects, valuably complement the results achieved with DTG and with flame ionization detection.

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Zusammenfassung Ein Atomabsorptionsspektrometer wurde mit einem konventionellen thermoanalytischen Quarzofen gekoppelt um thermische Abspaltprodukte nachzuweisen. In diesem kombinierten System wird das durch Kühlung des entwickelten Dampfes erhaltene Aerosol (Rauch) vom Ofen in die Flamme für den metallspezifischen Atomabsorptionsnachweis übergeleitet. Die spezielle Ausbildung der Austrittsöffnung gewährleistet die Bildung eines stabilen Aerosols. Die optimalen Versuchsbedingungen wurden durch Zinkchloridlösungen bei Anderung der Probenmasse, der Aufheizgeschwindigkeit und der Strömungsgeschwindigkeit des Ofengases im linearen Temperaturprogramm ermittelt. Die mit dieser Methode für verschiedene Zinkverbindungen erhaltenen Absorptions—Temperatur-Kurven wurden mit den entsprechenden DTG-Kurven verglichen. Die Anwendbarkeit dieser Technik bei dem Studium heterogener Reaktionen mit Kohlenstofftetrachlorid und Hexandämpfen wird gezeigt. Der Einsatz eines mit einer Quarzküvette zum Nachweis der thermischen Entwicklung von Quecksilberdampf versehenen Atomabsorptionsspektrometers wird beschrieben, sowie die Nachweisgrenze durch molekulare Absorption (für NO und NH₃) und Lichtstreuung (für aus organischem Material entwickelten Rauch). Die bei den beschriebenen Methoden erhaltenen Ergebnisse können, in mancher Hinsicht, die durch DTG und Flammenionisationsnachweis erhaltenen Ergebnisse wertvoll ergänzen.

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- , , . (), , . . , . — , , -. . - , , , ( NO NH₃) ( , ). , , , - .

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Presented in part at the 24th Hungarian Conference on Analytical Sptecroscopy, Miskolc, June 15–18, 1981. Abstracts pp. 159–162.

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The authors wish to express their thanks to S. Gál for his assistance in the present application of the temperature programmer developed by him and his group, and for the valuable discussions on the subject. Thanks are also due to K. Tomor and J. Kmives who participated in the comparative thermoanalytical measurements and their analysis.     

Investigation of transitions and relaxation processes in polystyrene by using positron annihilation

The glass transition and relaxation processes in polystyrene resins with the number average molecular weight ranging from 7.0·10² to 9.8·10⁴ were studied with the positron annihilation technique. The pick-off annihilation lifetime of ortho-positronium (₃) and its intensity (I ₃) were measured in the temperature range from 20 to 430 K. The glass transition temperature (T _g) was determined as an onset temperature coefficient of ₃.T _g shows the molecular weight dependence in these samples. BelowT _g, local motions were detected by measurements ofI ₃. The local motions could be observed above 100 K in this experiment.I ₃ show the minimum at around 250 K and it does not show molecular weight dependence.     

Thermogravimetry and differential scanning calorimetry of natural and synthetic melanins

The thermal stability of natural melanins from bovine eyes, black human hair and the hard core of banana peel, synthetic melanins obtained enzymatically or by autoxidation of various precursors, and chemically modified synthetic melanins was studied by DSC and TG analysis. It was shown that the resistance of melanins to thermal degradation depends on their origin. Synthetic melanins were found to be more stable to thermal decomposition than natural melanins. Methylation of melanins caused a significant increase in thermal stability. The DSC curves of melanins reveal typical relaxation phenomena in the temperature range 293–413 K.

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Zusammenfassung Mittels DSC und TG wurde die thermische Stabilität von natürlichen Melaninen aus Rindsaugen, aus schwarzem menschlichen Haar und aus Hartteilen von Bananenschalen, weiterhin von enzymatisch oder durch Autoxidation aus verschiedenen Präkursoren synthetisierten Melaninen sowie von chemisch modifizierten synthetischen Melaninen untersucht. Es zeigte sich, daß die Beständigkeit von Melaninen gegenüber thermischem Abbau von ihrem Ursprung abhängt. Synthetische Melanine erwiesen sich in der thermischen Zersetzung als stabiler als Melanine natürlichen Ursprunges. Durch Methylierung wird eine eindeutige Steigerung der thermischen Stabilität verursacht. Im Temperaturbereich 293–413 K zeigen weisen die DSC-Kurven der Melanine typische Relaxationserscheinungen auf.

     

Preparation and properties of yttrium complexes with alkanodicarboxylic acids

Malonate, succinate and glutarate of yttrium were obtained by dissolving Y(OH)₃ in a solution of the corresponding acid and crystallization, whereas adipate, pimelate, suberate, azelate and sebacate in the reaction of YCl₃ with the ammonium salt of the acid. Yttrium alkanodicarboxylates were prepared as crystalline solids with general formula Y₂O₃.nH₂O, wheren=3, 4, 6, 7. On the basis of IR spectra the way of coordination COO^– - Y³⁺ was established. Yttrium malonate, succinate, glutarate, azelate and sebacate heated lose crystallization water and next anhydrous complexes are transformed to Y₂O₃, whereas yttrium adipate, pimelate and suberate on heating lose some water molecules and, the mono- or dihydrates formed are decomposed to Y₂O₃. The properties of the studied complexes change discretely according to odd or even number of carbon atoms in the chain.

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Zusammenfassung Durch Auflösen von Y(OH)₃ in einer Lösung der entsprechenden Säure und anschliessendem Kristallisieren wurden Yttriummalonat,-succinat und -glutarat dargestellt, das Yttriumadipat, -pimelat-, -suberat und -azelainat und sebacate hingegen in der Reaktion von YCl₃ mit dem Ammoniumsalz der Säure. In Form kristalliner Feststoffe wurden Yttriumalkanodicarboxylate der allgemeinen Formel Y₂L₃,nH₂O mitn=3, 4, 6 bzw. 7 hergestellt. Ausgehend von den IR-Spektren konnte die Art der Koordinierung als COO^– y³⁺ festgestellt werden. Beim Erhitzen geben Ytrriummalonat, -succinat, -glutarat, azelainat und -sebazat ihr Kristallwasser ab, aus den anhydratierten Komplexen bildet sich anschliessend Y₂O₃, während Yttriumadipet, pimelat und -suberat einige Wassermoleküle verlieren und die monooder dihydratierten Formen sich dann zu Y₂O₃ zersetzen. Die Eigenschaften der untersuchten Komplexe variieren eindeutig in Abhängigkeit davon, ob sich in der Kette eine gerade oder ungerade Anzahl von Kohlenstoffatomen befindet.

     

Photobinding of ketoprofen in vitro and ex vivo

Ketoprofen (KP), a non-steroidal anti-inflammatory drug of the 2-aryl propionic class, has been shown to produce photoallergic side effects as well as cutaneous photosensitizing properties that induce other phototoxic effects. In the present study we investigated photobinding of ketoprofen to both human serum albumin (HSA), a model protein, and to ex vivo pig skin and its photodegradation. Results demonstrate that photoadduct formation and photodegradation progressively increased with irradiation time where they reach a maximum. Maximum photobinding to the viable layer of the epidermis was about 7-8% of the initial radiolabelled KP added, in the region of 15-30 min UV irradiation. These results were comparable to in vitro results that were seen with photobinding of KP to HSA; in this case, the quantity of covalently bound material was approximately 10% of the initial, after a maximum of 18 min irradiation. It was found by HPLC analysis that the KP decrease is accompanied by an increase of the corresponding photoproduct, decarboxylated ketoprofen (DKP). The yield of DKP reaches a maximum at around 15 min. DKP appears to play an important role in vitro and ex vivo, being the major photoproduct and responsible for the photobinding process. Using micro-autoradiographical techniques we investigated the penetration and distribution of ketoprofen in ex vivo pig skin in greater detail. It was apparent that percutaneous absorption was taking place and that most of the ketoprofen was predominately localised in fibroblasts in the papillary dermis. No other specific localisation within the skin architecture was identified. Although there were differences in the quantities of bound ketoprofen within the different layers of the skin, these levels did not appear to correlate with irradiation time.     

Expanded scope in ethylene-alkyne cross-metathesis: coordinating heteroatom functionality at the propargylic position

The Grubbs 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene-substituted ruthenium complex 1 catalyzed ethylene-alkyne cross-metathesis and was shown to tolerate free hydroxyl groups and coordinating functionality at the propargylic and homopropargylic positions. Hindered and enantiomerically enriched 1-substituted alkynes also react efficiently under the reported conditions.