English
| dc.contributor.author | Atac, A | |
| dc.contributor.author | Karaca, C | |
| dc.contributor.author | Gunnaz, S | |
| dc.contributor.author | Karabacak, M | |
| dc.date.accessioned | 2024-07-18T11:58:25Z | |
| dc.date.available | 2024-07-18T11:58:25Z | |
| dc.description.abstract | PERGAMON-ELSEVIER SCIENCE LTD | |
| dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/7356 | |
| dc.language.iso | Article | |
| dc.publisher | 1386-1425 | |
| dc.subject | The structure of 4,5-dimethyl-o-phenylenediamine (C8H12N2, DMPDA) was investigated on the basis of spectroscopic data and theoretical calculations. The sterochemical structure was determined by FT-IR, FT-Raman, UV, H-1 and C-13 NMR spectra. An experimental study and a theoretical analysis were associated by using the B3LYP method with Gaussian09 package program. FT-IR and FT-Raman spectra were recorded in the region of 4000-400 cm(-1) and 4000-10 cm(-1), respectively. The vibrational spectra were calculated by DFT method and the fundamental vibrations were assigned on the basis of the total energy distribution (TED), calculated with scaled quantum mechanics (SQM) method with Parallel Quantum Solutions (PQS) program. The UV absorption spectrum of the compound that dissolved in ethanol solution were recorded in the range of 190-400 nm. Total density of state (TDOS) and partial density of state (PDOS) of the DMPDA in terms of HOMOs and LUMOs were calculated and analyzed. Chemical shifts were reported in ppm relative to tetramethylsilane (TMS) for H-1 and C-13 NMR spectra. The compound was dissolved in dimethyl sulfoxide (DMSO). Also, H-1 and C-13 chemical shifts calculated using the gauge independent atomic orbital (GIAO) method. Mullikan atomic charges and other thermo-dynamical parameters were investigated with the help of B3LYP (DFT) method using 6-311++G** basis set. On the basis of the thermodynamic properties of the title compound at different temperatures have been carried out, revealing the correlations between heat capacity (C), entropy (S), enthalpy changes (H) and temperatures. The optimized bond lengths, bond angles, chemical shifts and vibrational wavenumbers showed the best agreement with the experimental results. (C) 2014 Elsevier B.V. All rights reserved. | |
| dc.title | English | |
| dc.type | DENSITY-FUNCTIONAL THEORY | |
| dc.type | JET-COOLED ANILINE | |
| dc.type | AB-INITIO | |
| dc.type | IONIZATION SPECTROSCOPY | |
| dc.type | DIMERIC STRUCTURES | |
| dc.type | DFT CALCULATIONS | |
| dc.type | FORCE-FIELDS | |
| dc.type | N-OXIDE | |
| dc.type | METHYLANILINE | |
| dc.type | ENERGY |