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• W2087704414 abstract "Comprehensive studies of the molecular and electronic structures, vibrational frequencies, and infrared and Raman intensities of the aniline radical cation, C6H5NH2+ have been performed by using the unrestricted density functional (UB3LYP) and second-order Møller–Plesset (UMP2) methods with the extended 6-311++G(df,pd) basis set. For comparison, analogous calculations were carried out for the closed-shell neutral aniline. The studies provided detailed insight into the bonding changes that take place in aniline upon ionization. The natural bond orbital (NBO) analysis has revealed that the pπ-radical conjugative interactions are of prime importance in stabilizing the planar, quinoid-type structure of the aniline radical cation. It is shown that the natural charges calculated for aniline are consistent with the chemical properties of this molecule (an ortho- and para-directing power of the NH2 group in electrophilic substitutions), whereas Mulliken charges are not reliable. The theoretical vibrational frequencies of aniline, calculated by the B3LYP method, show excellent agreement with the available experimental data. In contrast, the MP2 method is deficient in predicting the frequencies of several modes in aniline, despite the use of the extended basis set in calculations. The frequencies of aniline radical cation, calculated at the UB3LYP/6-311++G(df,pd) level, are in very good agreement with the recently reported experimental data from zero kinetic energy photoelectron and infrared depletion spectroscopic studies. The clear- cut assignment of the IR and Raman spectra of the investigated molecules has been made on the basis of the calculated potential energy distributions. Several bands in the spectra have been reassigned. It is shown that ionization of aniline can be easily identified by the appearance of the very strong band at about 1490 cm−1, in the Raman spectrum. The redshift of the N–H stretching frequencies and the blueshift of the C–H stretching frequencies are observed in aniline, upon ionization. As revealed by NBO analysis, the frequency shifts can be correlated with the increase of electron density (ED) on the antibonding orbitals (σNH*) and decrease of ED on σCH*, respectively. These effects are associated with a weakening of N–H bonds and strengthening of C–H bonds in the aniline radical cation. The simulated theoretical Raman and infrared spectra of aniline and its radical cation, reported in this work, can be used in further spectroscopic studies of their van der Waals clusters and hydrogen bonded complexes." @default.
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• W2087704414 date "2003-06-09" @default.
• W2087704414 modified "2023-10-14" @default.
• W2087704414 title "Electronic structures, vibrational spectra, and revised assignment of aniline and its radical cation: Theoretical study" @default.
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• W2087704414 doi "https://doi.org/10.1063/1.1574788" @default.
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