Basicity and Nucleophilicity Effect in Charge Transfer of AlH3-Base Adducts: Theoretical Approach
Affiliation:
1 Department Matter Sciences, Faculty of Sciences and Technology, University of Abbas Laghrour Khenchela, Algeria
2 Laboratory of Materials and Living Chemistry Activity-Reactivity (LCMV-AR); University of Batna1, Algeria
3 Department of Medicine, Faculty of Medicine, University of Batna2, Algeria
hafied_meriem@yahoo.fr
DOI:
https://doi.org/10.23939/chcht17.02.221
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Abstract:
This study permits to explore the interactions involved in Lewis acid (AlH3) and Lewis bases: CO; H2O; NH3; PH3; PC13; H2S; CN–; OH–; O2–2; F–; N(CH3)3; N2; N2H4; N2H2; C5H5N; C6H5-NH2. By means of DFT theory calculations with B3LYP functional using 6-31G(d,p) basis set and in order to check the effects of both the donor and the acceptor in the establishment of the different adducts we focused mainly on the calculation of the energetic gap ∆EHOMO-LUMO, Gibbs energies ∆G, the angle (θ) in AlH3-base and the interaction energy values Einter. The several parameters of the reactivity (electrophilicity index (ω), nucleophilicity (N), chemical potential (μ), hardness (η), and polarizability (α)) are also calculated to define the weak interaction as well as to distinguish between the nucleophilicity and basicity of different Lewis bases. The results showed that the electronic charge transfer is estimated to be important in the systems where the interaction is established between Al and anionic bases, and the electron donor power is predictable for O–2, F–, OH–, and CN–. The pseudo-tetrahedral adduct arrangements depend on the parameter geometries (bond length interaction and θ angle) and Gibbs energies ∆G characterizing the main stability.
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