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Why are rhodanines less efficient reagents in Diels–Alder reactions than isorhodanines? A quantum chemical study.
- Source :
- Journal of Molecular Modeling; Jul2019, Vol. 25 Issue 7, pN.PAG-N.PAG, 1p
- Publication Year :
- 2019
-
Abstract
- The reactivity of the 5-arylidenerhodanine and 5-arylideneisorhodanine derivatives in reactions with dimethyl maleate was computationally studied at the DFT(M06-2X)/6–311+G(d,p) theory level. Eight stereoisomers of the reaction products were considered. The effect of the solvent was taken into account by means of the continuous and discrete models for acetic acid (PCM and three CH<subscript>3</subscript>COOH molecules). Aromatic stabilization of the transition states was documented by the values of HOMA, NICS(0), and NICS(1) indices. The higher reactivity of the isorhodanine derivative was associated with a relatively low activation energy, ∆E<subscript>a</subscript> (15.2–22.3 kcal mol<superscript>–1</superscript>), which is needed to cross the TS. For the rhodanine derivative, higher values of ∆E<subscript>a</subscript> (34.1–36.1 kcal mol<superscript>–1</superscript>) were obtained. The reactivity was also studied from the perspective of the frontier molecular orbitals, the energy gaps between the HOMO and LUMO, the flux of electron density, the Fukui functions, f<superscript>+</superscript>(r), f<superscript>−</superscript>(r), and f<superscript>0</superscript>(r), and the global indexes defined in the conceptual DFT, i.e., the electronic chemical potential, chemical hardness, global electrophilicity, and empirical nucleophilicity index. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 16102940
- Volume :
- 25
- Issue :
- 7
- Database :
- Complementary Index
- Journal :
- Journal of Molecular Modeling
- Publication Type :
- Academic Journal
- Accession number :
- 137471931
- Full Text :
- https://doi.org/10.1007/s00894-019-4063-y