2011
Effects of Bentonite on p-Methoxybenzyl Acetate: A Theoretical Model for Oligomerization via an Electrophilic-Substitution Mechanism. Manuel Salmón, Rene Miranda, Ines Nicolás-Vázquez, Yolanda Marina Vargas-Rodríguez, Julián Cruz-Borbolla, María Isabel Medrano, José Antonio Morales-Serna. Molecules, 16, 1761-1775 (2011). ISSN: 1420-3049 doi:10.3390/molecules16021761
Abstract
Tonsil Actisil FF, a commercial bentonitic clay, promotes the formation of a series of electrophilic-aromatic-substitution products from para-methoxybenzyl acetate in carbon disulfide. The molecules obtained correspond to linear isomeric dimers, trimers, tetramers and a pentamer, according to their spectroscopic data. A clear indication of the title mechanistic pathway for the oligomerization growth was obtained from the analysis of a set of computational-chemistry calculations using the density-functional-theory level B3LYP/6-311++G(d,p). The corresponding conclusions were based on the computed dipole moments, the HOMO/LUMO distributions, and a natural-populations analysis of the studied molecules.
Mild Oxidation of C?C Bonds of Benzoiridacycles
Pyrite?Arsenopyrite Galvanic Interaction and Electrochemical Reactivity
Synthesis, characterization, and crystal structures of n-alkyldiorganodithiophosphates RS2P(OC6H4)2