In a previous paper (J. Phys. Chem. A2009, 113, 9721), we analyzed theoretically the Diels−Alder cycloaddition between cyclopentadiene and C60 for which experimental results on energy barriers and reaction energies are known. One of the main conclusions reached was that the two-layered ONIOM2(B3LYP/6-31G(d):SVWN/STO-3G) method provides results very close to the full B3LYP/6-31G(d) ones. Unfortunately, however, both the exothermicity of the reaction and the energy barrier were clearly overestimated by these two methods. In the present work, we analyze the effect of the inclusion of Grimme’s dispersion corrections in the energy profile of this reaction. Our results show that these corrections are essential to get results close to the experime...
Combining total energy calculations with a search of phase space, we investigate the microscopic fus...
We have measured the kinetic energy released in the unimolecular dissociation of fullerene ions, C(n...
The Diels–Alder reactivity of C59NH azafullerene has been explored computationally. The regioselecti...
The current paper is aimed at the determination of barriers that govern the covalent coupling betwee...
This dissertation involves explorations of on surfaces and on carbon-based nanomaterials, especially...
The Diels-Alder reactivity of different bowl-shaped polycyclic aromatic hydrocarbons (namely, corann...
The physical and chemical properties of fullerenes and nanotubes can be conveniently tuned by the at...
We have computationally studied the factors governing the enhanced Diels-Alder reactivity of noble g...
A discrete summation method has been developed to calculate the dispersion interaction potential bet...
One of the most important reactions in fullerene chemistry is the Diels–Alder (DA) reaction. In two ...
The physical factors governing the regioselectivity of the double functionalization of fullerenes ha...
We have used quantum chemistry computations, in conjunction with isodesmic-type reactions, to obtain...
Controlling the regioselectivity in the exohedral functionalization of fullerenes and endohedral met...
The exohedral reactivity of endohedral fullerene has aroused significant interest because of its pot...
The Diels–Alder reaction between C60 and [3]dendralene has been carried out using density functional...
Combining total energy calculations with a search of phase space, we investigate the microscopic fus...
We have measured the kinetic energy released in the unimolecular dissociation of fullerene ions, C(n...
The Diels–Alder reactivity of C59NH azafullerene has been explored computationally. The regioselecti...
The current paper is aimed at the determination of barriers that govern the covalent coupling betwee...
This dissertation involves explorations of on surfaces and on carbon-based nanomaterials, especially...
The Diels-Alder reactivity of different bowl-shaped polycyclic aromatic hydrocarbons (namely, corann...
The physical and chemical properties of fullerenes and nanotubes can be conveniently tuned by the at...
We have computationally studied the factors governing the enhanced Diels-Alder reactivity of noble g...
A discrete summation method has been developed to calculate the dispersion interaction potential bet...
One of the most important reactions in fullerene chemistry is the Diels–Alder (DA) reaction. In two ...
The physical factors governing the regioselectivity of the double functionalization of fullerenes ha...
We have used quantum chemistry computations, in conjunction with isodesmic-type reactions, to obtain...
Controlling the regioselectivity in the exohedral functionalization of fullerenes and endohedral met...
The exohedral reactivity of endohedral fullerene has aroused significant interest because of its pot...
The Diels–Alder reaction between C60 and [3]dendralene has been carried out using density functional...
Combining total energy calculations with a search of phase space, we investigate the microscopic fus...
We have measured the kinetic energy released in the unimolecular dissociation of fullerene ions, C(n...
The Diels–Alder reactivity of C59NH azafullerene has been explored computationally. The regioselecti...