| dc.description.abstract | The eld of computer simulations has developed into a very important branch of science providing a guess at
the interactions between molecules to obtain predictions of properties as accurate as required, subject to the
limitations imposed by the computer power and of the chosen and feasible theory level. Quantum chemical
methods are predominantly applied to isolated molecules, which corresponds to the state of an ideal gas. Most
chemical processes, however, take place in condensed phase, and the interaction of a molecule with its environment:
the dimension and the huge amount of degrees of freedom of the system preclude the possiblity of quantum-level
calculations.
In this PhD thesis di erent approaches to treat several aspects of structure and reactivity, through the use of
molecular dynamics techniques have been used.
In the rst part, behaviour of Ru complexes relevant as (pre)catalysts for ole n metathesis have been inves-
tigated. In particular, it has shed light on a so far underestimated key feature, i.e. the exibility around the
N substituent: this allows NHCs to modulate their encumbrance in the rst coordination sphere of the metal to
allow the coordination even for incoming bulky substrates.
Furthermore, the reduced electron density on the MO of the methylidene group, due to the presence of a acid
ligand trans have been analyzed, showing that it allows for a favorable interaction with the aromatic system of
the proximal mesityl group of the NHC ligand, which leads to metallacycle rst and subsequently in the formation
of a tensioned cyclopropane structure that nally evolves to the experimental product via a Buchner type ring
expansion. Since the presence of a transition metal and the bonds breaking/formation the quantum approach is
mandatory.
On the other hand, the structure description of a Metal/polymer interface have been treated with classical coarse
grained molecular dynamics approach. The calculated radial density pro les allowed to get atomistic insights in
the Metal/polymer interface. In both cases of non coated and coated gold nanoparticles the polystyrene chains
expose the phenyl rings to the nanoparticle surface. In the case of coated nanoparticles there is some penetration
of the polystyrene phenyl rings into nanoparticle coating layer. When it is present, the third organic component
(8 hydroxyquinoline) is closer to the nanoparticle surface and when in contact with a coated nanoparticle shows
a deeper penetration into the thiols layer. The orientation of 8 hydroxyquinoline results short range and parallel
with respect to the surface of non coated gold nanoparticles. Di erent is the 8 hydroxyquinoline orientation in the
case of a coated gold nanoparticle. In this case the orientation results perpendicular to the nanoparticle surface.[edited by author] | en_US |
