Theoretical Study of the Chemical Reactivity of Five Schiff Bases Derived From Dapsone by the DFT Method

Jean Stéphane N’dri

Laboratoire de Thermodynamique et de Physico-Chimie du Milieu, UFR SFA, Université Nangui Abrogoua, 02 BP 801 Abidjan 02, Côte-d’Ivoire

Mamadou Guy-Richard Koné *

Laboratoire de Thermodynamique et de Physico-Chimie du Milieu, UFR SFA, Université Nangui Abrogoua, 02 BP 801 Abidjan 02, Côte-d’Ivoire

Charles Guillaume Kodjo

Laboratoire de Thermodynamique et de Physico-Chimie du Milieu, UFR SFA, Université Nangui Abrogoua, 02 BP 801 Abidjan 02, Côte-d’Ivoire and Laboratoire de Chimie BioOrganique et de Substances Naturelles, Université Nangui Abrogoua, UFR-SFA, 02 B.P. 801 Abidjan 02, Côte-d’Ivoire

Ahmont Landry Claude kablan

UFR des Sciences Biologiques, Université Péléforo Gon Coulibaly de Korhogo, BP 1328 Korhogo, Côte d’Ivoire

Sopi Thomas Affi

Laboratoire de Thermodynamique et de Physico-Chimie du Milieu, UFR SFA, Université Nangui Abrogoua, 02 BP 801 Abidjan 02, Côte-d’Ivoire

Lamoussa Ouattara

Laboratoire de Thermodynamique et de Physico-Chimie du Milieu, UFR SFA, Université Nangui Abrogoua, 02 BP 801 Abidjan 02, Côte-d’Ivoire

Nahossé Ziao

Laboratoire de Thermodynamique et de Physico-Chimie du Milieu, UFR SFA, Université Nangui Abrogoua, 02 BP 801 Abidjan 02, Côte-d’Ivoire

*Author to whom correspondence should be addressed.


Abstract

This theoretical study of chemical reactivity was conducted using the method of the Density Functional Theory (DFT), with B3LYP/6-311G (d, p) as calculation level. A series of five (05) Schiff bases derived from 4.4 '-diaminodiphenylsulfone (Dapsone) was concerned and allowed to predict the chemical reactivity of these compounds. Molecular geometries and electronic properties such as the energies of the frontier molecular orbitals (HOMO and LUMO), ionization potential (I), and electron affinity (A) were examined to obtain a better overview of the molecular properties. Thus compound 4, whose energy gap between the frontier orbitals (HOMO and LUMO) is ΔEgap = 3.910 eV appears to be the most polarizable. It is the most reactive with the lowest kinetic stability compared to all the studied molecules. The values of the global reactivity descriptors confirmed the great chemical reactivity of the compound 4. Local indices of reactivity and dual descriptors were calculated to indicate the probable sites of Electrophilic and nucleophilic attacks of the various studied compounds.

Keywords: Chemical reactivity, global descriptors, local descriptors, dual descriptors


How to Cite

N’dri, Jean Stéphane, Mamadou Guy-Richard Koné, Charles Guillaume Kodjo, Ahmont Landry Claude kablan, Sopi Thomas Affi, Lamoussa Ouattara, and Nahossé Ziao. 2018. “Theoretical Study of the Chemical Reactivity of Five Schiff Bases Derived From Dapsone by the DFT Method”. Chemical Science International Journal 22 (4):1-11. https://doi.org/10.9734/CSJI/2018/41427.

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