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• W1600129251 abstract "In this study, we proposed to examine the reactivity of the intramolecular cycloaddition Diels-Alder (IMDA) reaction of the molecule triene amide by chemical descriptors established globally in the intermolecular reactions (DA), such as of electrophilic index ω and the nucleophilic index N. In order to provide the power releasing or withdrawing of electrons of the diene (D) and dienophile (Dp) fragments in the intramolecular molecule, the polarity of the reaction can be evaluated by the application of these two factors, applied locally to the diene (D) and dienophile (Dp) fragments, other parameters have been introduced to enrich these results, such as transferability index γ and charge transfer (CT) in a transition state. During our study we used density functional theory (DFT) in the hybrid B3LYP and basis set level 6-31G (d, p), the geometries are optimized for the reactants, transition states as well for products, the calculation of the charge transfer is carried out using the natural population analysis (NPA), the results obtained show that the diene (D) fragment is donor of electrons in the IMDA reaction." @default.
• W1600129251 created "2016-06-24" @default.
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• W1600129251 date "2014-06-06" @default.
• W1600129251 modified "2023-09-25" @default.
• W1600129251 title "Quantitative study by the Electrophilic and Nucleophilic indexes of chemical reactivity for the intramolecular Diels-Alder reaction of the Triene-Amide Molecule. DFT investigation" @default.
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• W1600129251 doi "https://doi.org/10.48317/imist.prsm/morjchem-v2i2.1912" @default.
• W1600129251 hasPublicationYear "2014" @default.
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