Does the Molecular Electrostatic Potential Reflect the Effects of Substituents in Aromatic Systems?

Substituent Effects on Non-Covalent Interactions with Aromatic Rings: Insights from Computational Chemistry

(2011) Rajesh K. Raju et al.   CHEMPHYSCHEM

Molecular electrostatic potential for exploring π-conjugation: a density-functional investigation

(2011) Subhash S. Pingale   PHYSICAL CHEMISTRY CHEMICAL PHYSICS

The electrostatic potential: an overview

(2011) Jane S. Murray et al.   Wiley Interdisciplinary Reviews-Computational Molecular Science

Electrophile Affinity: Quantifying Reactivity for the Bromination of Arenes

(2010) Boris Galabov et al.   JOURNAL OF ORGANIC CHEMISTRY

Appraisal of Through-Bond and Through-Space Substituent Effects via Molecular Electrostatic Potential Topography

(2010) Fareed Bhasha Sayyed et al.   JOURNAL OF PHYSICAL CHEMISTRY A

Through-Space Effects of Substituents Dominate Molecular Electrostatic Potentials of Substituted Arenes

(2009) Steven E. Wheeler et al.   Journal of Chemical Theory and Computation

Effects of Heteroatoms on Aromatic π−π Interactions: Benzene−Pyridine and Pyridine Dimer

(2009) Edward G. Hohenstein et al.   JOURNAL OF PHYSICAL CHEMISTRY A

Electrophile Affinity: A Reactivity Measure for Aromatic Substitution

(2009) Gergana Koleva et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Substituent Effects in Cation/π Interactions and Electrostatic Potentials above the Centers of Substituted Benzenes Are Due Primarily to Through-Space Effects of the Substituents

(2009) Steven E. Wheeler et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Predicting Reactivities of Organic Molecules. Theoretical and Experimental Studies on the Aminolysis of Phenyl Acetates

(2008) Boris Galabov et al.   JOURNAL OF PHYSICAL CHEMISTRY A

Origin of the SN2 Benzylic Effect

(2008) Boris Galabov et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Substituent Effects in the Benzene Dimer are Due to Direct Interactions of the Substituents with the Unsubstituted Benzene

(2008) Steven E. Wheeler et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY