Polymerization of propylene catalyzed over highly active and stereospecific catalysts synthesized with Mg(OEt)2/benzoyl chloride/TiCl4

A series of monoester catalysts has been studied, each catalyst prepared by the reaction of magnesium diethoxide with benzoyl chloride [BzCOCl, to produce ethyl benzoate (EB) in situ] in the presence of excess titanium tetrachloride. Solid product and catalysts obtained by subsequent treatments with titanium tetrachloride were characterized by elemental analysis, IR spectroscopy, x-ray diffraction, BET measurement, and thermal gravimetric analysis. The catalysts yielded very high activity (above 20 kg polymer/g Ti h atm) for the polymerization of propylene in slurry reactions. From the results of polymerization as well as catalyst characterization, the effects of internal and external Lewis bases on the isospecificity and stability of catalysts are discussed in detail. © 1992 John Wiley & Sons, Inc.     

On generating regular elements in the semigroup of binary relations

We prove the semigroup generated by four binary relations contains all regular binary relations.     

Social systems analysis

We present a model of social systems as special types of games in extensive form in which perception and learned strategies play an important role. We discuss personality, emotions, and the relation of utility to Maslow's hierarchy of values. We also formulate a new class of games, partially cooperative games, and attempt to define a solution concept for these.     

Pteridines. Part CVI. Isolation and characterization of limipterin (1-O-(L-erythro-biopterin-2′-yl)-β-N-acetylglucosamine) and its 5,6,7,8-tetrahydro derivative from green sulfur bacterium Chlorobium limicola f. thiosulfatophilum NCIB 8327

A new pteridine compound was isolated from green sulfur photosynthetic bacteria, Chlorobium limicola f. thiosulfatophilum NCIB 8327. The structure of this pterin derivative was established to be 1-O-(L -erythro-5,6,7,8- tetrahydropterin-2′-yl)-β-N-acetylglucosamine ( 1 ) from ¹H-NMR and CD spectra as well as from various mass spectrometric techniques and chemical-cleavage techniques. Upon acid hydrolysis of 1 , equimolar amounts of biopterin ( 2 ) and N-acetylglucosamine were produced. The structure of the hydrolysis product 2 was confirmed by comparing its NMR, UV, CD, and MS and its chromatographical behavior with those of an authentic specimen. N-Acetylglucosamine was identified by an enzymatic hydrolysis experiment as well as by NMR and thin layer chromatography. Electrospray (ES), fast-atom-bombardment (FAB), and thermospray (TS) mass spectrometry of 1 yielded an MH⁺ at m/z 441. Periodate-oxidation experiments of the intact molecule 1 and of its hydrolysis product 2 are consistent with the proposed structure. Differential I₂ oxidation experiments with the native compound showed that the in vivo oxidation state of this pterin is its tetrahydro form. We propose the trivial name ‘limipterin’ for this new compound.     

A sensitive radiochemical assay for Coenzyme A

Summary A simple and sensitive assay for Coenzyme A (CoA) is described. The method is based on coupling the enzymatic reactions of acetyl-CoA synthetase and acetyl-CoA carboxylase. CoA is converted into acetyl-CoA with acetyl-CoA synthetase in the presence of excess ATP and acetate. Acetyl-CoA is subsequently converted into malonyl-CoA with acetyl-CoA carboxylase in the presence of excess ATP and KH¹⁴CO₃. The formation of labelled acid-stable material (i.e. malonyl-CoA) is determined. Under conditions of the assay CoA is quantitatively converted into malonyl-CoA. This procedure permits the detection of as little as 15 pmoles of CoA in biological samples. Elimination of acetyl-CoA synthetase from the reaction mixture allows for the determination of acetyl-CoA.

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Empfindlicher radiochemischer Assay für Coenzym A

Zusammenfassung Ein einfacher und empfindlicher Assay für Coenzym A (CoA) wird beschrieben, der auf einer Kopplung der enzymatischen Reaktionen von Acetyl-CoA-synthetase und Acetyl-CoA-carboxylase beruht. CoA wird mit Hilfe von Acetyl-CoA-synthetase in Gegenwart von überschüssigem ATP und Acetat zu Acetyl-CoA umgesetzt. Dieses wird anschließend mit Acetyl-CoA-carboxylase in Gegenwart von überschüssigem ATP und KH¹⁴CO₃ zu Malonyl-CoA umgewandelt. Die Bildung von markierter säurestabiler Substanz (d.h. Malonyl-CoA) wird bestimmt. Unter den Versuchsbedingungen ist die Umsetzung von CoA zu Malonyl-CoA quantitativ. Noch 15 pMol CoA können in biologischem Material erfaßt werden. Durch Entfernung von Acetyl-CoA-synthetase aus dem Reaktionsgemisch kann auch Acetyl-CoA bestimmt werden.