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91.
The 837 keV resonance is used for the rapid and non-destructive determination of the gradient of fluorine on the surface of metallic samples. The precise yield curve of this resonance for thick target and the experimental sensitivity of the method have been determined. With this method less than 5·10?4 μg·cm?2 fluorine content can be measured. The resolution is of the order of 1000 Å in aluminium and the concentration profiles can be measured to the depth of 1 μm. The time requirement of a surface analysis is 15–30 min, and 2–3 hrs of a gradient measurement. In addition, this method is simpler and more sensitive than the detection of the 1350 keV alpha-particles from the19F(p, αo)16O reaction. 相似文献
92.
G. Zigeuner R. Hopmann Ch. Knopp A. Fuchsgruber 《Monatshefte für Chemie / Chemical Monthly》1970,101(6):1829-1830
Dihydro-6-styryl-2(1H)-pyrimidinones react with dienophiles such as maleic anhydride in form of aDiels—Alder reaction. 相似文献
93.
A new and efficient formal total synthesis of (3S,4S)-balanol, a potent protein kinase C inhibitor, was accomplished from tri-O-acetyl-d-glucal. Balanol and ophiocordin consists of a chiral hexahydro azepine-containing fragment and a benzophenone fragment. The azepine core was prepared in chiral form through intramolecular aza Wittig reaction. A triphenylphosphine mediated ring expansion process was employed to form the seven-membered nitrogen heterocycle. The aldehyde equivalent key intermediate was treated with triphenylphosphine to give the azepine core. To demonstrate the applicability of the new route, a synthesis of the balanol is described. 相似文献
94.
Portilla Y Chávez I Arancibia V Loeb B Manríquez JM Roig A Molins E 《Inorganic chemistry》2002,41(7):1831-1836
In this work, we report the synthesis and a study on the degree of electronic delocalization in the asymmetric mixed valence complexes [CpFe(C(8)H(6))Fe(C(8)H(7))](+), 3a(+), and [CpCo(C(8)H(6))Fe(C(8)H(7))](+), 3b(+), (Cp = C(5)Me(5), C(8)H(6) = pentalenyde, C(8)H(7) = hydropentalenyde, and = ((3,5(CF(3))(2)C(6)H(3))(4)B(-))). Electrochemical methods, (57)Fe M?ssbauer spectroscopy, electronic spectroscopy, and electron paramagnetic resonance were used for this purpose. Although the anti conformation of the complexes precludes any metal-metal interaction, all the techniques employed show that 3a(+) is a electronic delocalized system, while 3b(+) behaves as two individual metallic centers with localized electron density. 相似文献
95.
I. Golicheff M. Loeuillet Ch. Engelmann 《Journal of Radioanalytical and Nuclear Chemistry》1974,22(1-2):113-129
The experimental device used is described. Excitation functions are given for an angle of observation 150° with respect to
the incident beam. The possibilities of applying these reactions to the measurement of surface lithium and fluorine concentrations
are considered. The detection limits for these two elements are shown to be 5·10−3 μg·cm−2 with protons of energy between 1,350 and 1,500 keV. The method is compared with that based on the detection of prompt γ-rays
from the reactions7Li(p, γ)8Be and19F(p, α γ)16O.
相似文献
96.
Potential surfaces, dipole moments, and polarizabilities are calculated by ab initio methods [unrestricted MP2(full)/6-311++G(2d,2p)] along the reaction paths of the F+CH4 and Cl+CH4 reaction systems. It is found that in general dipole moments and polarizabilities exhibit peaks near the transition state. In the case of X=F these peaks are on the products side and in the case of X=Cl they are on the reactants side indicating an early transition state in the case of fluorine and a late transition state in the case of chlorine. An analysis of the geometric changes along the reaction paths reveals a one-to-one correspondence between the peaks in the electric properties and peaks in the rate of change of certain internal geometric coordinates along the reaction path. Interaction with short infrared intense laser fields pulses leads to the possibility of interferences between the dipole and polarizability laser-molecule interactions as a function of laser phase. The larger dipole moment in the Cl+CH4 reaction can lead to the creation of deep wells (instead of energy barriers) and new strongly bound states in the transition state region. This suggests possible coherent control of the reaction path as a function of the absolute phase of the incident field, by significant modification of the potential surfaces along the reaction path and, in particular, in the transition state region. 相似文献
97.
V. Yu. Mitskyavichyus R. S. Baltrushis I. Ch. Bilinskaite É. É. Liepin'sh R. M. Zolotoyabko 《Chemistry of Heterocyclic Compounds》1991,27(9):999-1006
The reaction of o-substituted aromatic amines with methacrylic acid gave N-aryl--methyl--alanines, which were converted to dihydro-2,4-pyrimidinedione and dihydro-4-pyrimidinone-2-thione derivatives. The alkylation, acylation, and oximation of the dihydro-2,4-pyrimidinediones were accomplished. Conformational analysis of the compounds obtained was carried out by dynamic NMR methods.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1240–1247, September, 1991. 相似文献
98.
Summary A new simplified version of a closed on-column injector is introduced. Because of its design isobaric injection conditions do not have to be followed and a wide range of injection temperatures above the boiling point of the sample solvent can be chosen for on-column injections in capillary gas chromatography. Also, when following certain basic injection rules, injections of large sample volumes (20 l or more) give accurate and reproducible results without further problems.Presented at the 17th International Symposium on Chromatography, September 25–30, 1988, Vienna, Austria. 相似文献
99.
The interaction of ethidium bromide (2,7-diamino-10-ethyl-9-phenylphenanthridinium bromide; EB) with double stranded (ds) calf thymus DNA and thermally denatured single stranded (ss) DNA was studied in solution and at the electrode surface by means of transfer voltammetry using a carbon paste electrode (CPE) as working electrode in 0.2 M acetate buffer, pH 5.0. As a result of intercalation of this dye between the base pairs of dsDNA, the characteristic peak of dsDNA, due to the oxidation of guanine residues, decreased and after a particular concentration of EB a new peak at +0.81 V appeared, probably due to the formation of a complex between dsDNA and EB. The non-intercalated EB gives another peak, but at an increased concentration of the dye. A similar behaviour was observed during the interaction of the dye with ssDNA.Furthermore, the interaction of EB with ds, ss and supercoiled (sc) DNA was studied at the hanging mercury drop electrode (HMDE) surface by means of alternating current voltammetry in 0.3 M NaCl and 50 mM sodium phosphate buffer (pH 8.5) as supporting electrolyte. dsDNA yields a smaller peak at −1.42 V (peak III) compared to the one yielded by ssDNA, since the latter is a relaxed and more accessible form. By addition of EB into the buffer solution an increase of peak III was observed in the dsDNA form as well as in ssDNA resulting from their interaction with EB. Furthermore, the appearance of peak III in covalently closed circular scDNA after exposure to increasing concentrations of EB is a result of the introduction of ‘free ends’ in DNA affecting its structural integrity. 相似文献
100.
M. M. Abd-Elmeguid Ch. Sauer U. Köbler W. Zinn 《Zeitschrift für Physik B Condensed Matter》1985,60(2-4):239-248
X-ray diffraction,151Eu Mössbauer effect (ME) and magnetic susceptibility measurements have been performed to investigate the valence behavior and the magnetic interactions of the Eu ions in the intermetallic series Eu(Pd1–x
Au
x
)2Si2 (0x1) as a Forx>0.4 all experimental techniques are in agreement with each other and suggest a divalent 4f
7 ground state of the Eu ion. Belowx=0.4 the different methods lead to different results: while the lattice parameters and the ME isomer shift suggest an instable behavior of the valence the magnetic susceptibility proves a pure divalent 4f
7 ground state. These differences can be explained by assuming a partial extension of the 4f-shell radius such that the localized character of the 4f-electrons is preserved.Dedicated to B. Mühlschlegel on the occasion of his 60th birthday 相似文献