Cyclic deformation of aluminium and its alloys

The formation of slip bands is the main mechanism of cyclic deformation in pure Al. Their density, orientation and heights in polycrystalline Al were investigated during cycling. Types, sizes and densities of precipitates are responsible for the mode of cyclic deformation in AlCu4 pure alloy. In technical Al alloys intermetallic phases have detrimental effects on deformation homogeneity and largely govern the fatigue mechanism of the material and especially microcrack initiation.     

含氧光敏引发体系的研究——Ⅵ.二苯酮/三乙胺体系引发光聚合过程中的再次引发效应

过去,作者曾发表了多种光敏引发体系引发烯类单体光聚合的工作,在研究2,2-二甲氧基苯乙酮在氧存在下引发甲基丙烯酸甲酯光聚合时,结合在聚合物链端的引发剂碎片具有光化学活性,在光聚合反应中产生高分子自由基,发生再次聚合,出现高分子量     

Conformation and Crystal Structure of Dipyrrinones with Oxindole Components

 Pyrrole α-aldehydes (2-formyl-4,5-dimethyl-1H-pyrrole and 2-formyl-N-methylpyrrole) condense readily at C(3) of indolin-2-ones to give dipyrrinone analogs, such as (3Z)-[(4,5-dimethylpyrrol-2-yl)-methylidenyl]-indolin-2-one and (3E)-[(1-methylpyrrol-2-yl)-methylidenyl]-indolin-2-one. ¹H-NMR NOE analyses and X-ray crystallography confirm the syn-(Z) configuration for the former and the syn-(E) configuration for the latter. The former is stabilized by intramolecular hydrogen bonding. Molecular mechanics calculations of the latter indicate no energy difference between the syn and anti conformations.     

A Water-Soluble Synthetic Bilirubin with Carboxyl Groups Replaced by Sulfonyl Moieties

 The first symmetrical bilirubin analog with CO₂H groups replaced by SO₃H, 8,12-bis-(2-sulfo-ethyl)-3,17-diethyl-2,7,13,18-tetramethyl-(10H,21H,23H,24H)-bilin-1,19-dione, was synthesized from methyl (2,4-dimethyl-5-ethoxycarbonyl-1H-pyrrol-3-yl) acetate in nine steps via the sulfonic acid analog of xanthobilirubic acid (XBR) and isolated as its disodium salt. The sulfonic acid group was introduced at an early stage of the synthesis by reaction of an intermediate, ethyl 4-(2-bromoethyl)-3,5-dimethyl-1H-pyrrole-2-carboxylate, with sodium sulfite. The disodium bilirubin disulfonate exhibits NMR spectroscopic properties rather similar to those of the parent carboxylic acid, mesobilirubin-XIIIα; however, its UV/Vis spectra are blue-shifted and broadened relative to those of the parent compound. Like mesobilirubin, the disulfonate displays a positive exciton chirality circular dichroism spectrum, albeit with weaker Cotton effects, in a buffered aqueous solution (pH = 7.4) containing a 2:1 molar ratio of human serum albumin.     

Mikrochemie

Ohne Zusammenfassung     

Gamma-ray bursts from evaporating primordial black holes

It is believed that the detection of gamma-ray bursts from evaporating primordial black holes is highly improbable in the near future since the expected photon flux, consisting mainly of photons with energies ≳ GeV, is too low. Contrary to this point of view, we show that a large fraction of the black hole power at the final stage of evaporation (the last 10³ s) can be liberated as a burst of soft γ-ray emission of duration 10⁻¹–10³ s and luminosity 10²⁸–10³¹ erg/s in the energy range 0.1–1 MeV. According to our calculations of the black hole evaporation rate (within the Standard Model of elementary particles), when the black hole temperature exceeds approximately 10 GeV, the charged particle outflow from a black hole forms a well-defined plasma and can be described in the hydrodynamic approximation. In this case more than half of the rest energy of a black hole can be converted into soft gamma-rays due to the presence of the magnetic field with energy density comparable to that of charged particles. We consider various mechanisms leading to such transformation and estimate their efficiency. It is shown that, at least, some of the gamma-ray bursts detected by BATSE can be associated with evaporating black holes. Institute of Applied Physics, Russian Academy of Sciences, Nizhny Novgorod, Russia. Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Radiofizika, Vol. 41, No. 1, pp. 36–45, January, 1998.     

The effect of LH wave on the peripheral plasma of TM-1-MH tokamak

The work is devoted to the study of the LH wave effect on the peripheral plasma of the TM-1-MH tokamak. The observed enhancement of the ion saturated current in the limiter shadow is interpreted as heating of the peripheral ions by absorption of decay waves generated in this region due to the nonlinear wave-plasma interaction.     

Fluorescence detected circular dichroism of a red-shifted exciton-coupling chromophore <Emphasis Type="Italic">N</Emphasis>,<Emphasis Type="Italic">N</Emphasis>′-carbonyl-bridged dipyrrinone derivative using an ellipsoidal device

A fluorescent red-shifted exciton-coupling chromophore, N,N′-carbonyl-bridged dipyrrinone, was subjected to fluorescence-detected CD (FDCD) measurements as a primitive structure-elucidating probe with trans-1,2-cyclohexanediol template in several solvents under various instrumental conditions. With the help of a JASCO ellipsoidal mirror device FDCD465, a chloroform solution achieved the sensitivity enhancement by 50 times of the transmission CD and 5 times of the conventional FDCD. All FDCD spectra were completely free from the polarization artifacts. Correspondence: Tatsuo Nehira and David A. Lightner, Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-hiroshima 739-8521, Japan; Department of Chemistry, University of Nevada, Reno, Nevada 89557, USA.     

Exciton Chirality. (A) Origins of and (B) Applications from Strongly Fluorescent Dipyrrinone Chromophores

(A) The origin of exciton interaction and examples of its application to organic stereochemistry are presented. (B) N,N-Carbonyl-bridged dipyrrinones constitute a new class of highly fluorescent chromophores suitable for investigations of stereochemistry and absolute configuration. N,N-Carbonylxanthobilirubic acid esters are strongly fluorescent, with a fluorescence quantum yield (_F) 0.8, but produce only weak exciton CD from the trans-1,2-cyclohexanediol template. The ester of an analog with benzoic acid replacing propionic, N,N-carbonyl-8-(4-carboxyphenyl)-3-ethyl-2,7,9-trimethyl-(10H)-dipyrrin-1-one, exhibits strong fluorescence (_F=0.68, _em=493nm, _ex=422nm in CHCl₃) and UV-Vis absorption (21000 at 424nm) in organic solvents. Its diester with (1S,2S)-cyclohexanediol is fluorescent and exhibits exciton circular dichroism (=+15dm³·mol^–1·cm^–1, =432nm; =–4dm³·mol^–1cm^–1, =380nm) that correlates with the Exciton Chirality Rule.