Intramolecular hemiacetals. The acid-base-catalyzed ring-chain interconversion of 2-substituted 2-hydroxy-4,4-dimethylmorpholinium cations in aqueous solution.

The ring-chain tautomerism in aqueous solution of some aryl-substituted morpholinium salts (bromides), has been studied and equilibrium constants are reported. In the crystals the substrates exist entirely in their cyclic forms as hemiacetals, but in aqueous solution NMR measurements reveal that an equilibrium is established between the cyclic (hemiacetal) and the noncyclic (ketone) form, the degree of ring-opening being more pronounced with electron-donating aryl substituents at the carbonyl carbon. The kinetics of the ring-chain interconversion in water has been investigated spectrophotometrically by a 'pH jump' stopped-flow technique. General base catalysis is observed with a Br?nsted beta value apparently independent of substituent and equal to 0.60. The Hammett rho values for various base catalysts are close to those for very similar intermolecular reactions involving hemiacetal breakdown, leading to the suggestion of a 'normal' class n mechanism for base catalysis. For acid catalysis, however, a quite different situation is encountered, since no general acid but only (weak) catalysis by the hydronium ion can be detected. We believe this deviation from 'normal' general acid catalysis is caused by an electrostatic interaction, and we suggest that it might result from a change in the usual class e mechanism for general acid catalysis by a situation in which rate-limiting concerted proton transfer is replaced by rate-limiting preprotonation. This is supported by the observed drastic change in Hammett rho value for catalysis by the hydronium ion, compared with the 'normal' case. An interesting case is encountered for the 4-aminophenyl-substituted substrate, in which the amino group becomes protonated in acid solution, thus representing a new substituent. Despite this complication, the various equilibrium and rate constants may also be evaluated experimentally for this substrate.     

Plasma B-6 vitamer and plasma and urinary 4-pyridoxic acid concentrations in young women as determined using high performance liquid chromatography.

Plasma B-6 vitamer and plasma and urinary 4-pyridoxic acid concentrations of 21 young white women, 21-27 years, having radiomonitored pyridoxal 5'-phosphate and coenzyme stimulation of erythrocyte alanine aminotransferase activities indicative of adequate vitamin B-6 status were determined in an effort to establish normal ranges for plasma B-6 vitamers. B-6 vitamers and 4-pyridoxic acid were quantitated using reversed phase high performance liquid chromatography with fluorometric and ultraviolet detection. Pyridoxal phosphate values obtained by radioenzymatic and chromatographic, fluorometric and ultraviolet, assays were highly correlated as were pyridoxine phosphate values determined using both detectors. The B-6 vitamer and 4-pyridoxic acid values of these subjects should be of use in the establishment of normal ranges of these congeners in women.     

Violation of Bell’s inequality in neutral kaons system

We show by general considerations that it is not possible to test violation of the existing versions of Bell’s inequality in entangled neutral kaons system using experimentally accessible thin regenerators. We point out the loophole in the recent argument (A Bramon and M Nowakowski, Phys. Rev. Lett. 83, 1 (1999)) that claimed such a test to be possible.     

Certified reference materials for the quality control of analysis in the environment

Summary The Community Bureau of Reference (BCR) has undertaken the production of a wide range of certified reference materials (CRMs) for the improvement of accuracy and measurement harmony in various areas of concern at European Community level. This paper provides an overview of the sectors of the BCR-programme in the field of environment i.e. for water systems (water, sediment, biota), soil analysis (soil, fertiliser, waste), plant analysis (aquatic and terrestrial plants), analysis related to animals (e.g. muscle or liver) or man (e.g. industry and food).     

The missing part of the greenhouse effect

Summary Global average temperatures from 1860 to 1989 were analysed with a simple fitting procedure. The temperature records can be fitted with a rising exponential up to 1946 and with the same exponential minus an increasing cooling action from 1946 to 1989. It is shown that the results are compatible with the hypothesis of an albedo increase caused by SO₂ emissions. This hypothesis gives satisfactory explanations of the temperature drop in the years 1940–1970, of the different warming of the northern and southern hemispheres and of the slower warming observed over North America. The results give an indication that the greenhouse warming in the next years could be faster than predicted until now. Due to the relevance of its scientific content, this paper has been given priority by the Journal Direction.     

Green's temperature functions of massive scalar particles for finite matter density

An explicit expression is obtained for the Green's functions of a massive scalar field for nonnull temperatures and density in the form of a series in powers of m/T. The equivalence of the spectral-geometric approach and the temperature technique of Matsubara and Bernard is demonstrated. Corrections to the Stefan-Boltzmann law are obtained on the basis of the calculated Green's functions. The energy density is calculated in regions of high and low temperatures. The formulas obtained can prove to be useful in the discussion of the phase transition hadrons-quark-gluon plasma.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 7, pp. 32–40, July, 1991.     

Hamiltonian and recursion operators for two-dimensional scalar fields

The equation for the Noether operator is obtained. It gives the necessary conditions for complete integrability of the field equations. For several double-component models the Hamiltonian pairs and the recursion operators are presented.