Observation of the neutron radiative decay

The aim of this work is the experimental observation of and research into a rare neutron mode, the radiative beta decay, where a new particle, the radiative gamma quantum, is formed along with the expected decay products: a beta electron, a recoil proton, and an antineutrino. The discovery of this rare neutron decay mode was conducted through identification of triple-coincidence events: simultaneous registration of a beta electron, a proton, and a radiative gamma quantum. The ordinary neutron decay was registered by double coincidences of a beta electron and a recoil proton. The statistics collected allow one to deduce the branching ratio (BR) BR = (3.2 ± 1.6) × 10⁻³ (90% C.L.) in the gamma energy region greater than 35 keV. This value of BR is consistent with standard electroweak theory. The text was submitted by the authors in English. An erratum to this article is available at .     

Banach spaces which are somewhat uniformly noncreasy

We consider a family of spaces wider than r-UNC spaces and we give some fixed point results in the setting of these spaces.     

Nitrat

Ohne Zusammenfassung     

Substituted γ-lactones. Some observations on the synthesis and reactivity of 4-aroyl-3-hydroxy-2(5H)-furanones

The reaction pathway towards formation of 4-aroyl-3-hydroxy-2(5H)-furanones 1 from the base catalyzed reaction between an acetophenone, diethyl oxalate and formaldehyde was investigated. If methoxide was used as base, a transesterification was found to occur in the first step, while a side reaction, namely the retro Claisen reaction, was in competition with the desired lactone formation in the second step. The nature of the solvent and the acidic character of 1 as well as the basicity of the aminoarylene were found to have a profound influence on the course of the reaction of 1 with aminoarylenes.     

The thermodynamics of proton dissociation of adenine

The thermodynamic quantities associated with ionization of the N₁ and N₉ protons of adenine have been calorimetrically determined as a function of temperature. The H values for proton dissociation of these groups, with pK values of 4.19 and 9.92, were found to be 5.1 and 9.1 kcal/mole, respectively, at 25°C, =0.025. The C _p values for proton dissociation of these groups were estimated to be –11 and –17 cal/mole-deg. These results indicate that the large heat capacity changes observed during conformational transitions of polynucleotides are not the result of ionization of the bases.     

Substituted γ-lactones: On the structural elucidation of the reaction products from 4-aroyl-3-hydroxy-2(5H)-furanones and 1,2-diamines

The reaction pathway of 4-aroyl-3-hydroxy-2(5H)-furanones 1 with diamines depends on the nature of the amine as well as on the applied reaction conditions. Thus, the reaction of 1a-d with 5,6-diamino-1,3-dimethyluracil 5 led to the formation of two isomeric Schiff bases 7a-d and 8a-d . Conversely type 1 compounds reacted with 4,5-diaminopyrimidine 9 or 2,3-diaminopyridine 10 to form the mono acid-base adducts 11a and 11b respectively. When type 1 compounds were reacted with aliphatic diamines 13a-d or p-phenylenediamine and p-xylenediamine, respectively also an immediate formation of acid-base adducts 15a-f was observed. The reaction of a number of O-methylated type 1 compounds with 1,2-ethylenediamine afforded the novel seven-membered ring compounds 18a-d in good yields. The analogous reaction of O-alkylated 1a with o-phenylenediamine 2 or 2,3-diaminonaphthalene gave the expected tricyclic ring systems 19 or 20 .     

Electrochemical synthesis of nanostructured ZnO films utilizing self-assembly of surfactant molecules at solid-liquid interfaces

An electrochemical synthesis strategy for the production of nanostructured films was developed by combining self-assembly of surfactant-inorganic aggregates at solid-liquid interfaces and an electrodeposition process. Through this approach high quality nanostructured ZnO films were cathodically deposited from a plating solution containing 0.1 wt % of sodium dodecyl sulfate (SDS). The resulting ZnO films possess lamellar structures with two different repeat distances, d001 = 31.7 A and d001* = 27.5 A, both of which feature well-defined long range order. Due to kinetically controlled surfactant-inorganic assembly during the deposition process, the film exhibits a wide distribution of the stacking directions of the ZnO layers, which will allow facile access of the guest molecules and analytes to the interlayers. The synthetic mechanism used here can be generalized to generate nanostructured films of other semiconducting and metallic materials with architectures that cannot be assembled by other means.     

Indications for the Occurrence of Nitric Oxide Synthases in Fungi and Plants and the Involvement in Photoconidiation of Neurospora crassa*

Indications for the occurrence of nitric oxide synthases in Dictyostelium, Neurospora, Phycomyces and the leguminous plant Mucuna hassjoo as well as a physiological role of nitric oxide in Neurospora crassa are demonstrated. An exogenous nitric oxide donor, sodium nitroprus-side, inhibited light-stimulated conidiation in N. crassa. Specific inhibitors of nitric oxide synthase, like the arginine derivatives N^G-nitro-L-arginine (L-NA) and N^G-nitro-L-arginine-methyl ester (L-NAME), enhanced conidiation in darkness and in the light, whereas the stereo-isomer D-NAME was inactive. This communication reports to our knowledge the first time the presence of enzymatic activity of nitric oxide synthase in fungi and a higher plant and an effect of nitric oxide in fungal photophysiology.     

A facile synthesis of novel triazoloquinoxahnones and triazinoquinoxalinones

A series of 1-aryl-s-triazolo[4,3-a]quinoxalin-4-ones, 3 , were synthesized via the pyrolysis of the corresponding hydrazones, 6 . Thus, the cyclodehydrogenation occurred by refluxing them in an inert solvent (e.g. ethylene glycol) to give the triazoloquinoxalin-4-ones in a satisfactory yield. Using DMSO as a solvent for the above transformation afforded as a minor by-product an S-ylid. In contrast to earlier findings, annelation of a six-membered ring was successful and achieved through the pyrolysis of the pyruvate hydrazones derived of the quinoxalin-4-ones at ?230° to give the as-triazino[4,3-a]quinoxalin-5-ones, 4 . The reaction of 5 with acetylacetone afforded 3-(3′,5′-dimethylpyrazol-1-yl)-2(1H)-quinoxalinone, 10 . The structural assignments for the new compounds were based on their elemental analysis and spectroscopic data as well as an independent synthesis.