RESUMO
This work presents a theoretical detailed analysis of the surface-enhanced Raman spectroscopy (SERS) of the pyridine - Au20, pyridine - Ag20, and pyridine - Ag8Au12 model systems considering different symmetries of the clusters. In addition to the well-known Td geometry of this twenty atoms metal cluster, low energy structures have been analyzed (Cs and Cb). Density functional methodology with the use of PBE, PBE0, and scalar - relativistic pseudopotentials have been employed for the electronic structure calculations of these molecule-metal complexes. The projected state density analysis has shown a different behavior that distinguishes vertex (V) pyridine position from surface (S) adsorption site on both Td and Cs geometries. Adsorption of pyridine on the V position is always energetically favored as compared to S substitution. The chemical mechanism of enhancement has been analyzed through charge-transfer in the adsorption of pyridine to the metal cluster and charge-transfer excitations between both moieties. There is a close relationship between the amount of charge transfer from the pyridine molecule to the cluster and the SERS enhancements. The highest enhancement factors were obtained precisely for the Au20 cubic structure, where 102 order enhancements were calculated. A back - donation of charge triggers the highest enhancements obtained for this case. The bimetallic case also shows an improvement in the enhancements as compared to Td and Cs geometries. In addition, a direct relationship between resonant charge - transfer excitations in the 500-530 nm range and SERS enhancement have been obtained. Cs and cubic clusters show higher chemical enhancements than Td structures, thus representing a promise as SERS substrates.
RESUMO
We present a detailed theoretical characterization of the structure and interactions in dichlorine clathrate hydrate cages. In the case of the dodecahedral cage, there is clear evidence of the presence of halogen bonding, whereas in the tetrakaidecahedral cage, the expected signatures are there but in a weaker form. Comparison is made with the available structural data from x-ray experiments, where the rotational motion of dichlorine has been taken into account through Monte Carlo simulations illustrating delocalization effects associated with sampling multiple minima, specifically for the larger cage. Finally, the intermolecular potentials have been calculated with local correlation methods, and energy decomposition analysis has been applied to shed light on the nature of the interactions.
RESUMO
The guest-host intermolecular potentials for the valence excited states of Br2 in the tetrakaidecahedral(T) and pentakaidecahedral(P) clathrate cages have been calculated using ab initio local correlation methods. We find that the excited states are more strongly bound than the corresponding ground states even in the small T cage where bromine has a tight fit. The angular dependence of the interaction energies is quite anisotropic; this reflects in the corresponding electronic shifts where regions of maxima for blue-shifts in the T cage indicate the presence of halogen bonding. We predict a large temperature dependence of the electronic shifts and compare absolute values with recent experimental studies. This stringent test indicates the reliability of local correlation treatments to describe weak intermolecular forces in ground and excited states.