Theoretical studies of solvent effects on the reaction of complexing ethylene and nickel dithiolene have been carried out by calculating the molecular geometry, electron distribution, and frequency of all the stagnation points existing in the reaction potential profiles by means of density functional theory methods at the B3LYP/6-31G(d) level. On the basis of frequency analysis and statistical thermodynamic theory, some thermodynamic parameters for the titled compound have been obtained for different solvents. It is shown that the bond energy of ethylene and nickel dithiolene enhances with the increase of the solvent polarity. In addition, the frontier orbital energy gaps of the two transition states will increase, while those of the produc...
The studies presented in this dissertation focus on elucidating key aspects of the interaction of me...
Chelate-aryl and chelate-chelate stacking interactions of nickel bis(dithiolene) were studied at the...
In the present study, the reactivity of OH with Ni(X2C2H2)2 and Ni(X2C2H2)2- (where X = S or Se) was...
Theoretical studies of solvent effects on the reaction of complexing ethylene and nickel dithiolene ...
The influences induced by various terminal substituents and solvents on the reaction mechanism and c...
The formation of olefin complexes is of potential importance in the separation of olefins. The solve...
We studied the reaction mechanism for the reaction between bis[1,2-di(trifluoromethyl) ethylene-1,2-...
We investigated the reaction mechanism and thermochemical property of conjugated dienes or mono-olef...
Dithiolene-based complexes show great potential to be applied as materials for organic optoelectroni...
A theoretical density functional theory (DFT) study was employed to investigate solvent effects on a...
The electrochemically reversible binding of olefins by nickel bis(dithiolene) has been extensively ...
International audienceDensity functional theory (DFT) and ab initio computations are applied to exam...
Nickel dithiolene dyes, noted for their intense long-wavelength electronic transitions, have been no...
The thiol-ene reaction is one of the fundamental reactions in biochemistry and synthetic organic che...
Nickel bis(dithiolene) reversibly binds olefins via a known interligand binding mechanism, but the ...
The studies presented in this dissertation focus on elucidating key aspects of the interaction of me...
Chelate-aryl and chelate-chelate stacking interactions of nickel bis(dithiolene) were studied at the...
In the present study, the reactivity of OH with Ni(X2C2H2)2 and Ni(X2C2H2)2- (where X = S or Se) was...
Theoretical studies of solvent effects on the reaction of complexing ethylene and nickel dithiolene ...
The influences induced by various terminal substituents and solvents on the reaction mechanism and c...
The formation of olefin complexes is of potential importance in the separation of olefins. The solve...
We studied the reaction mechanism for the reaction between bis[1,2-di(trifluoromethyl) ethylene-1,2-...
We investigated the reaction mechanism and thermochemical property of conjugated dienes or mono-olef...
Dithiolene-based complexes show great potential to be applied as materials for organic optoelectroni...
A theoretical density functional theory (DFT) study was employed to investigate solvent effects on a...
The electrochemically reversible binding of olefins by nickel bis(dithiolene) has been extensively ...
International audienceDensity functional theory (DFT) and ab initio computations are applied to exam...
Nickel dithiolene dyes, noted for their intense long-wavelength electronic transitions, have been no...
The thiol-ene reaction is one of the fundamental reactions in biochemistry and synthetic organic che...
Nickel bis(dithiolene) reversibly binds olefins via a known interligand binding mechanism, but the ...
The studies presented in this dissertation focus on elucidating key aspects of the interaction of me...
Chelate-aryl and chelate-chelate stacking interactions of nickel bis(dithiolene) were studied at the...
In the present study, the reactivity of OH with Ni(X2C2H2)2 and Ni(X2C2H2)2- (where X = S or Se) was...