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A Corrected Benzene Nitration Three-Step Mechanism Derived by Dft Calculation and Mo Theory: Step 1 and Step 2 Both Have to Overcome Barriers and the Step 1 of Generating No 2+ is Rate-Controlling Step, Last Step 3 is a Spontaneous Lewis Acid-Base Neutralization
Electrophilic aromatic substitution and single‐electron transfer (SET) by the phenylium ion in the gas phase: characterization of a long‐lived SET intermediate
Reactivity of 2,2‐disubstituted quinazolinone towards electrophilic substitution: First in silico design to verify experimental evidence of quinazolinone‐based new organic compounds
Kinetic and mechanistic study of micellar effects in ammonium metavanadate/NaNO2-triggered nitration of phenols in aqueous bisulfate and acetonitrile medium
Catalytic properties at the nanoscale probed by surface x-ray diffraction and coherent diffraction imaging
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