A proper comparison between bond strengths of different atom pairs is relevant only for the same formal bond order (BO) of atomic interactions, e.g., for single bonds, because it is clear that the higher is the BO or the number of the electron pairs responsible of bonding, the stronger is the bond. For the metal–metal interactions, such a comparison of the bond strengths is especially problematic because formal BOs may differ from the effective ones by more than 1 v.u. (valence units). In this paper, we investigated the strength of bonding and its correlation to structural parameters (bond length/BO) for 24 metal-metal pairs. A simple way of the BO and bond-strength analysis was proposed and verified on the transition metal dimers. In contr...
Abstract. We have used density functional theory to obtain the binding curves for a variety of hypot...
The main topic of this Thesis is total-energy calculations of metallic systems, with and without ads...
In contrast to the increasing family of weak intermolecular interactions in main-group compounds (X–...
The importance of relativity and dispersion in metallophilicity has been discussed in numerous studi...
The metal–metal bond is central in the chemistry of polymetallic complexes. Many structural investig...
Pauling’s principles developed later in the bond valence model (BVM) are fundamental in description ...
Density functional theory (DFT) is a widely used method for predicting equilibrium geometries of org...
In order to understand the physics behind the surface properties and nano-scale phenomena, we are mo...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
The metal-metal bond is central in the chemistry of polymetallic complexes. Many structural investig...
Physical and mechanical properties of crystalline materials are commonly controlled by the atomic st...
Force-field parameters of the first row transition metals together with a few additional common elem...
Bond valence – bond length empirical correlations are of great interest in chemistry, biology, geolo...
Density functional theory (DFT) is a widely used method for predicting equilibrium geometries of org...
The problem of the nature of the interatomic farces in the elementary metals and in intermetallic co...
Abstract. We have used density functional theory to obtain the binding curves for a variety of hypot...
The main topic of this Thesis is total-energy calculations of metallic systems, with and without ads...
In contrast to the increasing family of weak intermolecular interactions in main-group compounds (X–...
The importance of relativity and dispersion in metallophilicity has been discussed in numerous studi...
The metal–metal bond is central in the chemistry of polymetallic complexes. Many structural investig...
Pauling’s principles developed later in the bond valence model (BVM) are fundamental in description ...
Density functional theory (DFT) is a widely used method for predicting equilibrium geometries of org...
In order to understand the physics behind the surface properties and nano-scale phenomena, we are mo...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
The metal-metal bond is central in the chemistry of polymetallic complexes. Many structural investig...
Physical and mechanical properties of crystalline materials are commonly controlled by the atomic st...
Force-field parameters of the first row transition metals together with a few additional common elem...
Bond valence – bond length empirical correlations are of great interest in chemistry, biology, geolo...
Density functional theory (DFT) is a widely used method for predicting equilibrium geometries of org...
The problem of the nature of the interatomic farces in the elementary metals and in intermetallic co...
Abstract. We have used density functional theory to obtain the binding curves for a variety of hypot...
The main topic of this Thesis is total-energy calculations of metallic systems, with and without ads...
In contrast to the increasing family of weak intermolecular interactions in main-group compounds (X–...