We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
σ- and π-electron contributions to the substituent effect: natural population analysis.
- Authors
Ozimiński, Wojciech P.; Dobrowolski, Jan C.
- Abstract
Two independent σ- and π- substituent effect descriptors, sEDA and pEDA, were constructed using the Natural Population Analysis (NPA) approach. The descriptors are based on parameters of 32 monosubstituted benzene molecules calculated at the B3LYP/6-31G** level which is easily applicable to large molecular systems. The sEDA and pEDA descriptors have a clear physical meaning—they show to what extent the σ and π electrons are donated or withdrawn by the substituent from the substituted system. The descriptors were successfully tested to be independent of either of the applicable theoretical methods (DFT or MP2), basis set (6-31G** or cc-pVTZ), and solvent presence. We also demonstrated that the sEDA descriptor described equally well methane derivatives, whereas the pEDA descriptor explained behavior of ethene derivatives. Moreover, the two descriptors work out well for as different molecular systems as triazoles. A comparison of the sEDA and pEDA descriptors with the selected well-known substituent effect scales shows that the sEDA descriptor correlates well (R = 0.961) with the Boyd & Boyd/Boyd– Edgecombe χ descriptor and that so does also the pEDA descriptor (R = 0.943) with the Taft–Topsom σR- resonance constant. Copyright © 2009 John Wiley & Sons, Ltd.
- Subjects
POPULATION; HUMAN ecology; BENZENE; AROMATIC compounds; MOLECULES; AVOGADRO'S law
- Publication
Journal of Physical Organic Chemistry, 2009, Vol 22, Issue 8, p769
- ISSN
0894-3230
- Publication type
Article
- DOI
10.1002/poc.1530