Inductive or Field Substituent Effect? Quantum Chemical Modeling of Interactions in 1‑Monosubstituted Bicyclooctane Derivatives

Inductive substituent constants were obtained for systems lacking the resonance effect. The application of the charge of the substituent active region concept to study the substituent effect in 1-X-substituted bicyclooctane derivatives (B3LYP/6-311++G** calculations, X = NMe₂, NH₂, OH, OMe, CH₃, H, F, Cl, CF₃, CN, CHO, COMe, CONH₂, COOH, NO₂, NO) has revealed inductive interactions, which are through bonds

Dependence of the Substituent Effect on Solvent Properties

The influence of a solvent on the substituent effect (SE) in 1,4-disubstituted derivatives of benzene (BEN), cyclohexa-1,3-diene (CHD), and bicyclo[2.2.2]­octane (BCO) is studied by the use of polarizable continuum model method. In all X–R–Y systems for the functional group Y (NO₂, COOH, OH, and NH₂), the following substituents X have been chosen: NO₂, CHO, H, OH, and NH₂. The substituent effect is characterized by the charge of the substituent active region (cSAR­(X)), substituent effect stabilization energy (SESE), and substituent constants σ or <i>F</i> descriptors, the functional groups by cSAR­(Y), whereas π-electron delocalization of transmitting moieties (BEN and CHD) is characterized by a geometry-based index, harmonic oscillator model of aromaticity. All computations were carried out by means of B3LYP/6-311++G­(d,p) method. An application of quantum chemistry SE models (cSAR and SESE) allows to compare the SE in water solutions and in the gas phase. Results of performed analyses indicate an enhancement of the SE by water. The obtained Hammett-type relationships document different nature of interactions between Y and X in aromatic and olefinic systems (a coexistence of resonance and inductive effects) than in saturated ones (only the inductive effect). An increase of electric permittivity clearly enhances communications between X and Y for BEN and CHD systems