ON THE INCOMPLETENESS OF A DESCENDING CHAIN OF EXTENSIONS OF IMPLICATIONAL S5

C5.ω is obtained by adding, schematically, to the strict-implicational fragment C5 of S5 the axiom ((p → q) → (q → p)) → (q → p). This paper presents a fully general proof that neither C5.ω nor any of a descending chain of its extensions is complete with respect to any class of frames, correcting the garbled details of a version skeched in an earlier paper (same Zeitschrift 31 (1985), 201-208).     

Temperature dependence of magnetization in nanocrystalline FeCoZr alloy

The temperature dependence of magnetization of a nanocrystalline Fe₆₀Co₃₀Zr₁₀ alloy annealed at various temperatures to varying crystal sizes was investigated down to 5 K in the field range up to 5 T. The fitting procedure gave T^3/2 as the leading term irrespective of the crystal size. We suggest that the increase of the coefficient by this term for smaller crystals may be connected to an increased relative volume of their surface.     

Complexes of 2,2′,2″-Nirtilotriphenol. Part IV. Cage Compounds with Phosphorus(III) and Phosphorus(V)

The ligand 2,2′,2″-nitrilotriphenol reacts with P(III) and P(V) compounds to form corresponding phosphorus complexes. Syntheses and NMR data of 2,2′,2″-nitrilotriphenyl phosphite ( II ), 2,2′,2″-nitrilotriphenyl phosphate ( III ) and of a hydrolysis product of II , 2,2′-[N-(2-hydroxyphenyl)imino]diphenly phosphonate ( IV ), are reported, as well as crystal structures of II and IV . Phosphite II shows a bicycloundecane framework; no N?Pinteraction is present. The phosphonate IV shows two coordinated and one dangling phenol group; the N-atom does not interact with the P-atom. Strong acids protonate II as well as III to form cations: in these, NMR evidence indicates coordination of the N-atom to the P-atom.     

Optical and neutron domain structure studies of amorphous ribbons

The domain configuration of amorphous ribbons with positive, vanishing and negative magnetostriction constant λ_s has been investigated by means of the longitudinal magneto-optical Kerr-effect and a three-dimensional neutron depolarization analysis. The influence of an external tensile stress on the domain arrangement depends on the sign and the magnitude of the magnetostriction constant and could be measured quantitatively in the depolarization experiment. With the aid of the optical observations domain models have been established; these models were tested and completed by means of an analytic calculation of the corresponding depolarization matrix and a comparison with experimental data. Domain reorientation processes within the ribbons under an imposed tensile stress were found to agree with theoretical predictions. The nearly nonmagnetostrictive alloys shows neither stripe domains nor simple wide domains but a more complicated structure with several layers of domains.     

Microbial Baeyer-Villiger Oxidation of Ketones by Cyclohexanone and Cyclopentanone Monooxygenase – A Computational Rational for Biocatalyst Performance

Summary. Recombinant Escherichia coli overexpressing Pseudomonas sp. NCIMB 9872 cyclopentanone monooxygenase (CPMO, EC 1.14.13.16) and Acinetobacter sp. NCIMB 9871 cyclohexanone monooxygenase (CHMO, EC 1.14.13.22) have been utilized in whole-cell Baeyer-Villiger biotransformations of prochiral bicycloketones. A significant difference in substrate acceptance and stereoselectivity was observed for bicyclo[3.3.0] and bicyclo[4.3.0] substrates. A plausible mechanism of these transformations was established by means of high level DFT/B3LYP calculations suggesting an essential difference in electronic requirements for a successful enzymatic conversion, which was similarly encountered in recombinant whole-cell mediated biooxidations. Some of the lactones produced in the biocatalytic Baeyer-Villiger oxidation represent key intermediates for the synthesis of indole alkaloids.