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排序方式: 共有291条查询结果,搜索用时 15 毫秒
1.
Musalov M. V. Yakimov V. A. Potapov V. A. Andreev M. V. Amosova S. V. 《Russian Journal of Organic Chemistry》2019,55(11):1809-1811
Russian Journal of Organic Chemistry - The reaction of selenium dichloride with methyl and ethyl propiolates leads to formation of anti-Markovnikov adducts. The regio- and stereoselective synthesis... 相似文献
2.
Crystallography Reports - The studies of wide-gap semiconductor materials using electron-beam induced current (EBIC) method are reviewed. The main methods for measuring the diffusion length of... 相似文献
3.
The hole thermal-emission rates and the cross sections for hole capture to the bound states in Ge quantum dots in Si are determined by admittance spectroscopy. The capture cross sections and the activation energies for emission rate are found to be related to each other by the Meyer-Neldel rule with a characteristic energy of 27±3 meV, which does not depend on the quantum-dot size. It is established that the capture cross section changes with temperature following the activation law. The experimental data are evidence of a unified multiphonon mechanism for the activation processes of hole transitions from the Ge quantum dots to the Si valence band and hole capture back into the quantum dots. 相似文献
4.
Mátyás Milen László Hazai Pál Kolonits György Kalaus Lajos Szabó Ágnes Gömöry Csaba Szántay 《Central European Journal of Chemistry》2005,3(1):118-136
Transformation of β-carboline derivatives into optically active entities were studied and the de and ee values of the resulted compounds were detected.
Dedicated to Professor Károly Lempert on his 80th birthday. 相似文献
5.
Milen Raytchev Elke Mayer Nicole Amann Hans-Achim Wagenknecht Torsten Fiebig 《Chemphyschem》2004,5(5):706-712
5-(Pyren-1-yl)-2'-deoxyuridine (PydU) and 5-(Pyren-1-yl)-2'-deoxycytidine (PydC) were used as model nucleosides for DNA-mediated reductive electron transport (ET) in steady-state fluorescence and femtosecond time-resolved transient absorption spectroscopy studies. Excitation of the pyrene moiety in PydU and PydC leads to an intramolecular electron transfer that yields the pyrenyl radical cation and the corresponding pyrimidine radical anion (dU.- and dC.-. By comparing the excited state dynamics of PydC and PydU, we derived information about the energy difference between the two pyrimidine radical anion states. To determine the influence of protonation on the rates of photoinduced intramolecular ET, the spectroscopic investigations were performed in acetonitrile, MeCN, and in water at different pH values. The results show a significant difference in the basicity of the generated pyrimidine radical anions and imply an involvement of proton transfer during electron hopping in DNA. Our studies revealed that the radical anion dC.- is being protonated even in basic aqueous solution on a picosecond time scale (or faster). These results suggest that protonation of dC.- may also occur in DNA. In contrast, efficient ET in PydU could only be observed at low pH values (< 5). In conclusion, we propose--based on the free energy differences and the different basicities--that only dT.- but not dC.- can participate as an intermediate charge carrier for excess electron migration in DNA. 相似文献
6.
Sergei D. Kirik Julia N. Zaitseva Igor S. Yakimov Nikolay N. Golovnev 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(11):i159-i160
Lithium sodium aluminium fluoride was obtained as a white powder by melting a stoichiometric mixture of AlF3, NaF and LiF at 1223 K, and then cooling to 923 K and sintering at this temperature for 4 h. The ab initio crystal structure determination was carried out using X‐ray powder diffraction techniques. The monoclinic structure of LiNa2AlF6 can be related to cubic elpasolite. The Li and Al atoms lie on inversion centres. The main octahedral AlF6 structural elements are not deformed, but are rotated slightly with respect to the unit‐cell axes. The Li atoms have octahedral coordinations, whereas the Na atoms have cubo‐octahedral coordinations. The Na coordination polyhedron is distorted in comparison with that of elpasolite. 相似文献
7.
J. Fekete M. Milen L. Hazai L. Poppe Cs. Szántay A. Kettrup I. Gebefügi 《Chromatographia》2003,57(3-4):147-153
Summary Reversed (RP-HPLC) and normal phase chromatographic (NP-HPLC) separations have been developed for diastereomers ofN-acyl-1-methyl-1,2,3,4-tetrahydo-β-carbolines which are acylated derivatives of simple natural β-carboline alkaloids. Separations
of derivatives having different acyl moieties in theO,O-diacyl-tartaric acid ester subtituent differed remarkably. Little or no resolution in either NP-HPLC or RP-HPLC could be
achieved with the diacetyl-tartrate derivative. Base-line separation by RP-HPLC but no separation by NP-HPLC was possible
with the bulkier and more apolar dipivaloyl derivative. Retention order of the bis-benzoylated diastereomers was reversed
and separation time increased dramatically by RP-HPLC. Good separation of the medium polarity, but rigid,N-camphanyl derivative by NP-HPLC has been achieved, whereas RP-HPLC could not be used for separation of these diastereomers.
Separability of different diastereomers was highly dependent on polarity and rigidity of the derivatizingN-acyl moieties. Conformational analysis by molecular mechanics and comparison of the lowest energy conformational states of
the diastereomers was applied to rationalise separation-retention behaviour of stereoisomers by RP-HPLC.
Presented at Balaton Symposium '01 on High-Performance Separation Methods, Siófok, Hungary, September 2–4, 2001 相似文献
8.
A. Yu. Yakimov 《Fluid Dynamics》2012,47(6):789-792
Steady-state free plane surface waves are investigated in the nonlinear formulation by means of the narrow streak method. The second-order differential equation derived can readily be integrated numerically. The first approximation of the equation is integrated. The next approximation leads to a nonlinear first-order differential equation which is traditional to the problem considered and whose coefficients have a simple physical meaning. 相似文献
9.
Spectra of the photocurrent of holes in δ-doped Si layers with Ge quantum dots in weak external electric fields have been studied. It has been established that the photocurrent of the holes in the photovoltaic mode changes its sign with the increase in the impurity concentration in the δ layers. It has been found that there is a voltage range in the vicinity of the zero bias in which the direction of the photocurrent is determined by the wavelength of the exciting radiation. 相似文献
10.