Uesugi, Y., Mizuno, M., Shimojima, A. and Takahashi, H. (1997) Transient Resonance Raman and Ab-Initio Mo Calculation Studies of the Structures and Vibrational Assignments of the t1 State and the Anion Radical of Coumarin and Its Isotopically Substituted Analogues. The Journal of Physical Chemistry, 101, 268-274.
https://doi.org/10.1021/jp9626881

has been cited by the following article:

• TITLE: Studies of the Chemical Reactivity of a Series of Rhodanine Derivatives by Approaches to Quantum Chemistry

  AUTHORS: Wacothon Karime Coulibaly, Jean Stéphane N’dri, Mamadou Guy-Richard Koné, Camille Déliko Dago, Christelle N’ta Ambeu, Jean-Pierre Bazureau, Nahossé Ziao

  KEYWORDS: Rhodanine Derivatives, Global Descriptors, Local Descriptors, Dual Descriptors

  JOURNAL NAME: Computational Molecular Bioscience, Vol.9 No.3, August 9, 2019

  ABSTRACT: This theoretical chemical reactivity study was conducted using the Density Functional Theory (DFT) method, at computational level B3LYP/6-31G (d). It involved a series of six (06) 5-arylidene rhodanines and allowed to predict the chemical reactivity of these compounds. DFT global chemical reactivity descriptors (HOMO and LUMO energies, chemical hardness, softness, electronegativity) were examined to predict the relative stability and reactivity of rhodanin derivatives. Thus, the compound 6 which has an energy gap between the orbitals of ΔEgap = 3.004 eV is the most polarizable, the most reactive, the least stable, the best electron donor and the softest molecule. Calculation of the local indices of reactivity as well as dual descriptors revealed that the sulfur heteroatom of the Rhodanine ring is the privileged site of electrophilic attack in a state of sp3 hybridization and privileged site of nucleophilic attack in a state of sp2 hybridization.