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1.
M. Yu. Anikovsky A. S. Tatikolov P. G. Pronkin P. P. Levin V. I. Sklyarenko V. A. Kuzmin 《High Energy Chemistry》2003,37(6):398-404
The influence of DNA on the cis–trans equilibrium and fluorescent properties of 3,3-diethyl-9-thiomethylthiacarbocyanine iodide (DTTC) in a phosphate buffer (pH 7) was studied by various photochemical techniques. The interaction of dye molecules with DNA leads to the formation of stable noncovalently bonded complexes. Data obtained from DTTC absorption and fluorescence spectra suggest that complexation proceeds primarily through the cis-form of the dye. Complexation with DNA leads to a substantial increase in the quantum yield of the triplet state of DTTC molecules. The rate constant for quenching the dye triplet state by oxygen turned out to be significantly lower than the diffusion-controlled value. 相似文献
2.
Electrochemical and electrocatalytic properties of thin films Au(111-25 nm), which are quasi-single-crystal electrodes 25
nm thick made of gold with the (111) preferential orientation, and same electrodes modified with a monolayer (ML) of palladium
are studied in 0.1 M solutions of HClO4 and H2SO4 employing voltammetric techniques and surface enhanced infrared reflection absorption spectroscopy (ATR-SEIRAS). Spectroscopic
experiments demonstrate strong adsorption of electrolyte species (H2O, OHads, anions) on the Pd surface. The weak and reversible adsorption of CO on Au(111-25 nm) does not change the interfacial-water
structure. Adsorption of CO on the Pd-modified film results in an irreversibly adsorbed CO adlayer stabilized by co-adsorbed
isolated water species. Various electrooxidation mechanisms are discussed. Electrochemical and spectroscopic investigations
on the adsorption and electrooxidation of HCOOH on bare and 1 ML Pd-Au(111-25 nm) electrodes reveal that electrooxidation
proceeds in both cases via a direct or dehydrogenation pathway. This mechanism involves the formation of formate as intermediate,
which is detected by in situ ATR-SEIRAS. The reactivity on Pd-modified surfaces is higher than on bare gold. The specifically
adsorbed anions (sulfate/bisulfate) and the oxide formation on the substrate surface lower the reactivity for CO and HCOOH
on both surfaces.
Published in Russian in Elektrokhimiya, 2006, Vol. 42, No. 11, pp. 1312–1329.
Based on the report delivered at the 8th International Frumkin Symposium “Kinetics of the Electrode Processes,” October 18–22,
2005, Moscow.
The text was submitted by the authors in English. 相似文献
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V. A. Keskinov A. K. Pyartman N. A. Charykov O. V. Arapov A. A. Pronkin V. V. Lishchuk V. V. Leonov 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2008,82(3):329-331
The phase diagram of the hexane-o-xylene-dimethylformamide ternary liquid system was studied at T= 298.15 K. The diagram contained the regions of homogeneous solutions and two-phase liquid systems (systems with stratification), phase I being enriched in dimethylformamide and phase II, in hexane. The distribution of fullerenes C60 and C70 was considered at various concentrations and simultaneous presence in sections at variable phase compositions. The extraction isotherms of fullerenes C60 and C70 under various conditions were found to be close to linear, and the C70/C60 separation factor depended on the composition of the coexisting phases and ranged from 1.25 to 1.8. Fullerene C70 was predominantly distributed in phase I. 相似文献
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本文利用KDV方程所对应的线性方程解所具有的光滑效应及压缩映像原理,得到了Hirota-Satsuma系统初值问题的局部和整体适定性结果. 相似文献
8.
P. G. Pronkin A. S. Tatikolov V. I. Sklyarenko V. A. Kuz’min 《High Energy Chemistry》2006,40(4):252-258
The processes of cis-trans photoisomerization and thermal back isomerization as well as the effect of DNA on the spectral and kinetic characteristics of the triplet state of a number of meso-substituted thiacarbocyanine dyes: 3,3’-diethyl-9-methoxythiacarbocyanine iodide (K1), 3,3’,9-triethylthiacarbocyanine iodide (K2), 3,3’-diethyl-9-methylthiacarbocyanine iodide (K3), and 3,3’-diethyl-9-chlorothiacarbocyanine perchlorate (K4), were studied by the flash photolysis method. Upon flash photoexcitation, the processes of trans-cis and cis-trans photoisomerization were observed for dye K1; the data on the structure of the absorption bands of the photoisomers were obtained. Complexation with DNA leads to an increase in the quantum yield of the triplet state of the dyes, which is explained by growing rigidity of the bound molecules. In the presence of DNA, triplet state deactivation follows the two-exponential law, thus showing that the dyes form complexes of two different types. The processes of quenching of the dye triplet state by oxygen were studied in solutions and in complexes with DNA. The rate constants for oxygen quenching of the triplet state of the dyes in complexes with DNA were found to be much lower than the values expected for the diffusion-controlled reactions (with allowance for the spin statistical factor, $k_{qO_2 } < 1/9k_{dif} $ ), which is explained by the steric factor of the complexation. 相似文献
9.
Cis-trans equilibrium for a number of meso-substituted oxacarbocyanine dyes, 3,3′-diethyloxacarbocyanine iodide (K1), 3,3′-diethyl-9-methyloxacarbocyanine iodide (K2),
3,3′-dimethyl-9-ethyloxacarbocyanine iodide (K3), 3,3′,9-triethyl-6,6′-dimethoxyoxacarbocyanine iodide (K4), and 3,3′,9-triethyl-5,5′-dimethyloxacarbocyanine
iodide (K5), has been studied in solutions and in a complex with DNA by spectral and fluorescent methods. A shift of the cis-trans isomer equilibrium toward the formation of the trans-isomer was observed in the presence of DNA, which determined in many respects the spectral effects observed upon the complexation
of the oxacarbocyanine dyes. A steep rise of fluorescence (due to binding of the trans-isomer) in a complex with DNA is favorable for using oxacarbocyanine dyes to determine DNA. 相似文献
10.
The vibronic vapour phase photoacoustic spectrum of Br2 in the wavelength region 505–541 nm (19796–18480 cm−1) has been recorded using microphone as well as pump-probe method. Discrete vibronic bands superimposed on a monotonically
increasing continuum background towards the dissociation limit results from the overlapping B
3Π
0u
/+
← X
1Σ
g
/+
and 1Π1u
← X
1Σ
g
/+
electronic transitions. Vibronic bands originating from υ″=0 have been used to estimate the relative rate of non-radiative relaxation as a function of the excited state B
3Π0u
vibrational quantum number υ′. A comparison with the optical absorption spectroscopy of Br2 leads to the identification of three broad spectral regions between 505 and 541 nm (19796 and 18480 cm−1) on the basis of different non-radiative relaxation processes. 相似文献