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排序方式: 共有7254条查询结果,搜索用时 218 毫秒
81.
Yuan Ruo Cao ShuRui Chai YaQin Gao FengXian Zhao Qing Tang MingYu Tong ZhongQiang Xie Yi 《中国科学B辑(英文版)》2007,50(5):620-628
Alternate adsorption of positively charged colloid-Au nanoparticles (nano-Au⊕) and negatively charged hemoglobin (Hb) on L-cysteine (L-cys) modified gold electrode resulted in the assembly of {Hb/nano-Au⊕}n layer-by-layer films/L-cys modified gold electrode. The nano-Au⊕ was characterized by transmission electron micrograph (TEM) and microelectrophoresis. The modified electrode interface morphology was characterized by electrochemical impedance spectroscopy (EIS), atomic force mi- croscopy (AFM), cyclic voltammograms (CV) and chronoamperometry. Direct electron transfer between hemoglobin and gold electrodes was studied, and the apparent Michaelis-Menten constant ( km app) of the modified electrode was evaluated to be 0.10 mmol·L?1. Moreover, the higher activity of proteins in the nano-Au⊕ films could be retained compared with the electropolymerization membrane, since the pro- teins in nano-Au⊕ films retained their near-native structure. Direct electron transfer between hemoglo- bin and electrode and electrochemically catalyzed reduction of hydrogen peroxide on a modified elec- trode was studied, and the linear range was from 2.1×10-8 to 1.2 ×10?3 mol·L-1 (r = 0.994) with a detection limit of 1.1×10-8 mol·L-1 H2O2. 相似文献
82.
Chuan-Jin Guan 《Journal of fluorine chemistry》2003,119(1):97-100
Styrene oligomers with perfluoro[1-(2-fluorosulfonyl)ethoxy]ethyl end-groups have been synthesized with moderate to high yields (52-97%) via radical oligomerization by using perfluoro[2-(2-fluorosulfonyl)ethoxy]propyonyl peroxide (PPP) at various reactant ratios of styrene over PPP (80, 160, 240, 300, 360 and 420) and different temperatures (33, 37 and 42 °C), and characterized by FTIR, 1H NMR and 19F NMR. The molecular weight of the oligomers measured by gel permeation chromatography (GPC) is dependent on the reactant ratio and reaction temperature. The polydispersity of the oligomers varies from 1.99 to 3.30. The oligomer obtained at the reactant ratio of 300 has the maximum yield (97%) and much broader polydispersity (3.30). The contact angles of water, θH2O, on the oligomer films are much bigger than that of polystyrene (PS). The glass transition temperature of the oligomers, Tg, increases with the increase of molecular weight and is lower than that of the parent polymer. 相似文献
83.
M. V. Pryadeina Ya. V. Burgart M. I. Kodess V. I. Saloutin 《Russian Chemical Bulletin》2005,54(12):2841-2845
Cyclocondensation of 2-arylmethylidene-3-fluoroalkyl-oxopropionates with 2-amino-pyridine occurs at both the polyfluoroacylvinyl
and alkoxycarbonylvinyl fragments to give alkyl 4-aryl-2-polyfluoroalkyl-4H-pyrido[1,2-a]pyrimidine-3-carboxylates and 4-aryl-2-hydroxy-3-polyfluoroacyl-4H-pyrido[1,2-a]pyrimidines, respectively. When treated with copper(II) acetate, the pyrido[1,2-a]pyrimidines yield metal complexes.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2745–2749, December, 2005. 相似文献
84.
The standard enthalpies of formation ΔfHo (liq. or cr.) at the temperature T = 298.15 K were measured using combustion calorimetry for benzophenone (A), 1-indanone (B), -tetralone (C), 9-fluorenone (D), anthrone (E) and dibenzosuberone (F). The standard enthalpies of vaporization ΔvHo or sublimation ΔsHo of A-F and 5,7-dihydro-6H-dibenzo[a,c]cyclohepten-6-one (G) were obtained from the temperature function of the vapor pressure measured in a flow system. Enthalpies of fusion ΔmH of solid compounds were measured by DSC. From the enthalpies of formation of the gaseous compounds of A-G the values of their strain enthalpies were derived and structural effects discussed.
85.
在硼氢化钾碱性溶液中对金属氢化物(MH)电极的表面进行化学还原处理,提高了MH电极的放电容量、活化性能和电催化活性.用其为负极组装的AA型MH-Ni电池进行了封口化成,电池放电容量达到1150mAh,5C下电池的放电容量达到0.2C下容量的80%以上,电池在1C100%DOD(放电深度)充放电条件下,循环寿命由原来的100次左右提高到200次以上 相似文献
86.
R. Sakamoto 《Colloid and polymer science》1984,262(10):788-792
Solvent effects on the phase separation of poly(-benzyl L-glutamate) to liquid crystal and isotropic solution have been observed in various helicogenic solvents. The temperature-composition phase diagrams have been determined for each solution. The critical concentrations,
2
*
, at which the phase separation occours have been compared in various solvents. In dimethylformamide in which the polymer is molecularly dispersed, the observed
2
*
value has agreed with that calculated by Flory's theory. In some solvents in which the polymer aggregates in a head-to-tail mode such as chloroform, the observed
2
*
values have been considerably small. It is assumed that the polymer aggregates behave as longer particles than the original particles. In dioxane in which the polymer aggregates highly both in a head-to-tail and a side-by-side modes, the
2
*
value has been a little larger than that in chloroform. In this case the relationship between the aggregation and the liquid crystal formation is so complicated that further investigation is necessary. In aromatic solvents such asm-cresol that dissolves the polymer almost molecularly, the
2
*
is smaller than that in dimethylformamide. Therefore, the intermolecular interactions between the phenyl groups in the side groups of the polymer and those in solvent molecules must be considered.The author is grateful to Mr. K. Sano and Mr. M. Watanabe for their observation of the liquid crystal formation. 相似文献
87.
The stoichiometric solubility constant of eitelite (NaMg
0.5
CO
3
+2H+ ⇄ Na++0.5Mg
2+
+CO
2
(g)+H
2
O, log*K
pso
I
=14.67±0.03 was determined at I=3 m (mol kg−1) (NaClO
4
) and 25°C. The stability of magnesium (hydrogen-)carbonato complexes in this ionic medium was explicitely taken into account.
Consequently, trace activity coefficients of free ionic species, calculated from the Pitzer model with ion-interaction parameters
from the literature, were sufficient for an evaluation of the thermodynamic solubility constants and Gibbs energies of formation
for eitelite (−1039.88±0.60), magnesite (−1033.60±0.40), hydromagnesite (−1174.30±0.50), nesquehonite (−1724.67±0.40), and
brucite (−835.90±0.80 kJ-mol
−1
). The increasing solubilities of nesquehonite and eitelite at higher sodium carbonate molalities were explained by invoking
a magnesium dicarbonato complex (Mg2++2CO
3
2−
⇄ Mg(CO3)
2
2−
, log βz = 3.90 ± 0.08). A set of ion-interaction parameters was obtained from solubility and dissociation constants for carbonic
acid in 1 to 3.5 m NaClO
4
media
which reproduce these constants to 0.02 units in log K. The following Pitzer parameters are consistent with the previously
studied formation of magnesium (hydrogen-)carbonato complexes in 3m NaClO
4
. The model and Gibbs functions of solid phases derived here reproduce original solubility data (−log [H+], [Mg
2+
]
tot
) measured in perchlorate medium within experimental uncertainty.
Presented at the XXII International Conference on Solution Chemistry, July 14–19, 1991, Linz, Austria. 相似文献
88.
E. V. Tulyakova O. A. Fedorova Yu. V. Fedorov G. Jonusauskas A. V. Anisimov 《Russian Chemical Bulletin》2007,56(11):2166-2174
Using 1H NMR spectroscopy and steady-state and time-resolved electronic spectroscopy, the optical properties of mono-and bis(styryl)pyridinium
perchlorates and their complexes with Mg2+, Ba2+ cations were studied. The stability constants of the complexes were determined using spectrophotometric titration. The formation
of inclusion complexes for Mg2+ and sandwich type complexes for Ba2+ results in fluorescence enhancement and increases the lifetimes of the excited states of the initial bis-styryl ligands.
The variation of position of the styryl fragment in the pyridinium aromatic ring gives rise to photochromic crown ethers with
different optical and photophysical characteristics and is also an easy route to bis(crown-ethers) of symmetrical and unsymmetrical
structure.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2092–2100, November, 2007. 相似文献
89.
Study on oxidation of polymers treated by high LET radiation 总被引:2,自引:0,他引:2
Wang Ruiyu Ha Hongfei Wang Yugang Zhao Weijiang Yan Sha Jin Changwen Wang Guanghui Wu Jilan 《Radiation Physics and Chemistry》1998,52(1-6):251-256
The oxidation of medical silicone rubber and segmented polyether urethane which were bombarded with 11.2 MeV Si+ or F+ at the dose of 5 × 1014 ions/cm2 was studied. In XPS measurements, it was found that the oxygen concentration on the surface of the implanted polymeric membranes had been increasing in three months at least. ESR measurement showed that some free radicals existed in these membranes and their quantities decreased with time. Chemical analysis proved that peroxides were generated in the γ irradiated membranes. The reason for the increasing of oxygen concentration was that free radicals combined with oxygen in the air and produced peroxides on the membrane surface. Moreover, in order to demonstrate the radiation mechanism, low LET (γ rays) radiation of such polymeric membranes was carried out for comparison 相似文献
90.
An optical biosensor for the determination of hydrogen peroxide based on immobilized horseradish peroxidase is described. The fluorescence of the dimeric product of the enzyme catalysed oxidation of homovanillic acid is utilized to determine the concentration of H2O2. The membrane-bound enzyme is attached to a bifurcated fibre bundle permitting excitation and detection of the fluorescence by a fluorometer. The response of the sensor is linear from 1 to 130 M hydrogen peroxide; the coefficient of variation is 3%. The sensor is stable for more than 10 weeks. The operating pH for maximal sensor response is 8.15. This allows the sensor to be used in combination with oxidase reactions producing hydrogen peroxide, as is demonstrated with a co-immobilized lactate oxidase-horseradish peroxidase optode for the determination of L-lactate. The fluorescence intensity of this sensor depends linearly on the concentration of lactate between 3 and 200 M and a throughput of 10 samples per hour is possible. The precision is in the same range as that of the monoenzyme optode. The lifetime of the bienzyme sensor for lactate is considerably shorter than that of the peroxidase sensor; it is limited by the stability of the immobilized lactate oxidase enzyme. The sensor has been applied to the determination of lactate in control serum. 相似文献