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<p style="margin-bottom: 0px; font-stretch: normal; font-size: 12px; line-height: normal; font-family: Helvetica; min-height: 14px;"><br></p><p style="margin-bottom: 0px; font-stretch: normal; font-size: 7px; line-height: normal; font-family: Helvetica;"><span style="font-stretch: normal; font-size: 12px; line-height: normal;"> </span>In this study, first, Benzene molecule pretends as the starting point, and then methyl and amine groups were added to construct Benzene like molecules. After that, the change of the mentioned physical properties above was investigated. In addition, HOMO-LUMO, MEP, and character tables of these organic molecules were obtained, and the effect of group symmetry was investigated. Density functional theory calculations were used in this study to obtain vibrational and electronic spectra for the four ring molecules (Benzene, Toluene, p-Xylene, p-Toluidine) and optimized geometries of molecules were performed in these programs. It was concluded that the molecules belong to D<span style="font-stretch: normal; font-size: 5px; line-height: normal;">6h</span>, C<span style="font-stretch: normal; font-size: 5px; line-height: normal;">2v</span>, D<span style="font-stretch: normal; font-size: 5px; line-height: normal;">2h </span>and C<span style="font-stretch: normal; font-size: 5px; line-height: normal;">2v </span>symmetry point groups for Benzene, Toluene, p-Xylene, and p-Toluidine respectively. It is concluded that lowest C1-C2 bond was in Benzene and p-Xylene, and the highest C1-C2 bond was in Toluene. On the other hand, it was found out that many vibrational frequencies changed with the addition of subgroups. It was aimed to determine the interaction sites of each molecule. For this purpose, mulliken atomic charges, molecular electrostatic potential (MEP) surface map and quantum chemical properties such as hardness, softness, electronegativity, chemical potential, ionization potential, electrophilic index, dipole moment, electron affinity were calculated via Gaussian program. </p> |
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