Investigation on the electroreduction azo coupling mechanism of 1,4-dinitrobenzene in aprotic media containing CO2

2022 ◽  
pp. 139841
Author(s):  
Feng Li ◽  
Yan Liu ◽  
Wenjuan Wang ◽  
Wei Wang ◽  
Baokang Jin
Keyword(s):  
Coupling Mechanism ◽  
Azo Coupling

EVALUATION OF TISSUE STEROID BINDING IN VITRO

1971 ◽  
Vol 68 (1_Suppl) ◽  
pp. S223-S246 ◽  
Author(s):  
C. R. Wira ◽  
H. Rochefort ◽  
E. E. Baulieu
Keyword(s):  
Protein Binding ◽  
Binding Sites ◽  
Experimental System ◽  
Specific Protein ◽  
Coupling Mechanism ◽  
Target Tissue ◽  
Protein Binding Sites ◽  
Definition Of ◽  
Hormone Specificity

ABSTRACT The definition of a RECEPTOR* in terms of a receptive site, an executive site and a coupling mechanism, is followed by a general consideration of four binding criteria, which include hormone specificity, tissue specificity, high affinity and saturation, essential for distinguishing between specific and nonspecific binding. Experimental approaches are proposed for choosing an experimental system (either organized or soluble) and detecting the presence of protein binding sites. Techniques are then presented for evaluating the specific protein binding sites (receptors) in terms of the four criteria. This is followed by a brief consideration of how receptors may be located in cells and characterized when extracted. Finally various examples of oestrogen, androgen, progestagen, glucocorticoid and mineralocorticoid binding to their respective target tissues are presented, to illustrate how researchers have identified specific corticoid and mineralocorticoid binding in their respective target tissue receptors.

Anionic and Cationic Redox Processes in β-Li2IrO3 and Their Structural Implications on Electrochemical Cycling in Li-Ion Cell

2019 ◽  
Author(s):  
Paul Pearce ◽  
Gaurav Assat ◽  
Antonella Iadecola ◽  
François Fauth ◽  
Rémi Dedryvère ◽  
...  
Keyword(s):  
Analytical Techniques ◽  
Charge Compensation ◽  
Coupling Mechanism ◽  
Redox Processes ◽  
Positive Electrodes ◽  
X Ray ◽  
Electrochemical Cycling ◽  
Li Ion ◽  
Electrochemical Instability ◽  
High Degree

The recent discovery of anionic redox as a means to increase the energy density of transition metal oxide positive electrodes is now a well established approach in the Li-ion battery field. However, the science behind this new phenomenon pertaining to various Li-rich materials is still debated. Thus, it is of paramount importance to develop a robust set of analytical techniques to address this issue. Herein, we use a suite of synchrotron-based X-ray spectroscopies as well as diffraction techniques to thoroughly characterize the different redox processes taking place in a model Li-rich compound, the tridimentional hyperhoneycomb β-Li2IrO3. We clearly establish that the reversible removal of Li+ from this compound is associated to a previously described reductive coupling mechanism and the formation of the M-(O-O) and M-(O-O)* states. We further show that the respective contributions to these states determine the spectroscopic response for both Ir L3-edge X-ray absorption spectroscopy (XAS) and X-ray photoemissions spectroscopy (XPS). Although the high covalency and the robust tridimentional structure of this compound enable a high degree of reversibile delithiation, we found that pushing the limits of this charge compensation mechanism has significant effects on the local as well as average structure, leading to electrochemical instability over cycling and voltage decay. Overall, this work highlights the practical limits to which anionic redox can be exploited and sheds some light on the nature of the oxidized species formed in certain lithium-rich compounds.<br>

Anionic and Cationic Redox Processes in β-Li2IrO3 and Their Structural Implications on Electrochemical Cycling in Li-Ion Cell

2019 ◽  
Author(s):  
Paul Pearce ◽  
Gaurav Assat ◽  
Antonella Iadecola ◽  
François Fauth ◽  
Rémi Dedryvère ◽  
...  
Keyword(s):  
Analytical Techniques ◽  
Charge Compensation ◽  
Coupling Mechanism ◽  
Redox Processes ◽  
Positive Electrodes ◽  
X Ray ◽  
Electrochemical Cycling ◽  
Li Ion ◽  
Electrochemical Instability ◽  
High Degree

The recent discovery of anionic redox as a means to increase the energy density of transition metal oxide positive electrodes is now a well established approach in the Li-ion battery field. However, the science behind this new phenomenon pertaining to various Li-rich materials is still debated. Thus, it is of paramount importance to develop a robust set of analytical techniques to address this issue. Herein, we use a suite of synchrotron-based X-ray spectroscopies as well as diffraction techniques to thoroughly characterize the different redox processes taking place in a model Li-rich compound, the tridimentional hyperhoneycomb β-Li2IrO3. We clearly establish that the reversible removal of Li+ from this compound is associated to a previously described reductive coupling mechanism and the formation of the M-(O-O) and M-(O-O)* states. We further show that the respective contributions to these states determine the spectroscopic response for both Ir L3-edge X-ray absorption spectroscopy (XAS) and X-ray photoemissions spectroscopy (XPS). Although the high covalency and the robust tridimentional structure of this compound enable a high degree of reversibile delithiation, we found that pushing the limits of this charge compensation mechanism has significant effects on the local as well as average structure, leading to electrochemical instability over cycling and voltage decay. Overall, this work highlights the practical limits to which anionic redox can be exploited and sheds some light on the nature of the oxidized species formed in certain lithium-rich compounds.<br>

Oxidation mechanism of carcinogenic bis-azo dyestuff Trypan Blue

1982 ◽  
Vol 47 (10) ◽  
pp. 2746-2748 ◽  
Author(s):  
Miroslav Matrka ◽  
Jana Pípalová
Keyword(s):  
Acid Medium ◽  
Quantitative Evaluation ◽  
Oxidation Product ◽  
Trypan Blue ◽  
Oxidation Mechanism ◽  
Azo Coupling ◽  
Arenediazonium Salt

Oxidation of Trypan Blue with cerium(IV) ion in acid medium gives arenediazonium cation similar to the oxidation product of N,N-dimethyl-4-aminoazobenzene. Quantitative evaluation of the arenediazonium salt formed has been carried out spectrophotometrically after previous C-azo coupling with 2-naphthol.

scholarly journals Remote Sensing of Ecosystem Water Use Efficiency: A Review of Direct and Indirect Estimation Methods

2021 ◽  
Vol 13 (12) ◽  
pp. 2393
Author(s):  
Wanyuan Cai ◽  
Sana Ullah ◽  
Lei Yan ◽  
Yi Lin
Keyword(s):  
Remote Sensing ◽  
Water Use Efficiency ◽  
Analytical Model ◽  
Water Use ◽  
Estimation Methods ◽  
Retrieval Algorithm ◽  
Canopy Conductance ◽  
Coupling Mechanism ◽  
Indirect Methods ◽  
Use Efficiency

Water use efficiency (WUE) is a key index for understanding the ecosystem of carbon–water coupling. The undistinguishable carbon–water coupling mechanism and uncertainties of indirect methods by remote sensing products and process models render challenges for WUE remote sensing. In this paper, current progress in direct and indirect methods of WUE estimation by remote sensing is reviewed. Indirect methods based on gross primary production (GPP)/evapotranspiration (ET) from ground observation, processed models and remote sensing are the main ways to estimate WUE in which carbon and water cycles are independent processes. Various empirical models based on meteorological variables and remote sensed vegetation indices to estimate WUE proved the ability of remotely sensed data for WUE estimating. The analytical model provides a mechanistic opportunity for WUE estimation on an ecosystem scale, while the hypothesis has yet to be validated and applied for the shorter time scales. An optimized response of canopy conductance to atmospheric vapor pressure deficit (VPD) in an analytical model inverted from the conductance model has been also challenged. Partitioning transpiration (T) and evaporation (E) is a more complex phenomenon than that stated in the analytic model and needs a more precise remote sensing retrieval algorithm as well as ground validation, which is an opportunity for remote sensing to extrapolate WUE estimation from sites to a regional scale. Although studies on controlling the mechanism of environmental factors have provided an opportunity to improve WUE remote sensing, the mismatch in the spatial and temporal resolution of meteorological products and remote sensing data, as well as the uncertainty of meteorological reanalysis data, add further challenges. Therefore, improving the remote sensing-based methods of GPP and ET, developing high-quality meteorological forcing datasets and building mechanistic remote sensing models directly acting on carbon–water cycle coupling are possible ways to improve WUE remote sensing. Improvement in direct WUE remote sensing methods or remote sensing-driven ecosystem analysis methods can promote a better understanding of the global ecosystem carbon–water coupling mechanisms and vegetation functions–climate feedbacks to serve for the future global carbon neutrality.

scholarly journals 5-((8-Hydroxyquinolin-5-yl)diazenyl)-3-methyl-1H-pyrazole-4-carboxylic Acid

Molbank ◽  
10.3390/m1238 ◽  
2021 ◽  
Vol 2021 (2) ◽  
pp. M1238
Author(s):  
Ion Burcă ◽  
Valentin Badea ◽  
Calin Deleanu ◽  
Vasile-Nicolae Bercean
Keyword(s):  
Chemical Structure ◽  
Functional Group ◽  
Coupling Reaction ◽  
2D Nmr ◽  
Azo Coupling ◽  
2D Nmr Spectroscopy ◽  
Azo Compound ◽  
Ft Ir ◽  
New Compounds ◽  
Carboxylic Functional Group

A new azo compound was prepared via the azo coupling reaction between 4-(ethoxycarbonyl)-3-methyl-1H-pyrazole-5-diazonium chloride and 8-hydroxyquinoline (oxine). The ester functional group of the obtained compound was hydrolyzed and thus a new chemical structure with a carboxylic functional group resulted. The structures of the new compounds were fully characterized by: UV–Vis, FT-IR, 1D and 2D NMR spectroscopy, and HRMS spectrometry.

scholarly journals Author Correction: Non-local effect of impurity states on the exchange coupling mechanism in magnetic topological insulators

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Thiago R. F. Peixoto ◽  
Hendrik Bentmann ◽  
Philipp Rüßmann ◽  
Abdul-Vakhab Tcakaev ◽  
Martin Winnerlein ◽  
...  
Keyword(s):  
Exchange Coupling ◽  
Topological Insulators ◽  
Local Effect ◽  
Coupling Mechanism ◽  
Impurity States ◽  
Non Local

A Correction to this paper has been published: https://doi.org/10.1038/s41535-021-00314-9

Intelligent optimization of EV comfort based on a cooperative braking system

2021 ◽  
pp. 095440702110044
Author(s):  
Lingying Zhao ◽  
Min Ye ◽  
Xinxin Xu
Keyword(s):  
System Model ◽  
Regenerative Braking ◽  
Coupling Mechanism ◽  
Intelligent Algorithm ◽  
Distribution Strategy ◽  
Braking System ◽  
Logic Diagram ◽  
Braking Torque ◽  
Braking Force ◽  
The Time Domain

To address the comfort of an electric vehicle, a coupling mechanism between mechanical friction braking and electric regenerative braking was studied. A cooperative braking system model was established, and comprehensive simulations and system optimizations were carried out. The performance of the cooperative braking system was analyzed. The distribution of the braking force was optimized by an intelligent method, and the distribution of a braking force logic diagram based on comfort was proposed. Using an intelligent algorithm, the braking force was distributed between the two braking systems and between the driving and driven axles. The experiment based on comfort was carried out. The results show that comfort after optimization is improved by 76.29% compared with that before optimization by comparing RMS value in the time domain. The reason is that the braking force distribution strategy based on the optimization takes into account the driver’s braking demand, the maximum braking torque of the motor, and the requirements of vehicle comfort, and makes full use of the braking torque of the motor. The error between simulation results and experimental results is 5.13%, which indicates that the braking force’s distribution strategy is feasible.

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