Mahalakshmi G, Balachandran V
Department of Physics, Karpagam University, Coimbatore 641021, India.
Research Department of Physics, Arignar Anna Government Arts College, Musiri, Tiruchirapalli 621211, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2014 Apr 24;124:328-40. doi: 10.1016/j.saa.2014.01.038. Epub 2014 Jan 21.
The FT-IR and FT-Raman spectra of 3,3'-bis (trifluoromethyl) benzophenone (TFMBP) were recorded and analyzed. Natural bond orbital analysis on TFMBP, 3,3'-bis (trichloromethyl) benzophenone (TCMBP) and 3,3'-bis (tribromomethyl) benzophenone (TBMBP) has been carried out for various intramolecular interactions that are responsible for the stabilization of the molecule. HOMO-LUMO energy gap of the halogen substitution (Cl, Br) has been computed with the help of density functional theory. The statistical thermodynamic functions (heat capacity, entropy, vibrational partition function and Gibbs energy) were obtained for the range of temperature 100-1000 K. The polarizability, first hyperpolarizability, anisotropy polarizability invariant has been computed using quantum chemical calculations. The infrared and Raman spectra were also predicted from the calculated intensities. Comparison of the experimental and theoretical spectra values provides important information about the ability of the computational method to describe the vibrational modes. UV-VIS spectral analyses of TFMBP have been researched by theoretical calculations. In order to understand electronic transitions of the compound, TD-DFT calculations on electronic absorption spectra in gas phase and solvent (DMSO and Chloroform) were performed. The calculated frontier orbital energies, absorption wavelengths (λ), oscillator strengths (ƒ) and excitation energies (E) for gas phase and solvent (water and methanol) are also illustrated.
记录并分析了3,3'-双(三氟甲基)二苯甲酮(TFMBP)的傅里叶变换红外光谱(FT-IR)和傅里叶变换拉曼光谱(FT-Raman)。对TFMBP、3,3'-双(三氯甲基)二苯甲酮(TCMBP)和3,3'-双(三溴甲基)二苯甲酮(TBMBP)进行了自然键轨道分析,以研究各种负责分子稳定的分子内相互作用。借助密度泛函理论计算了卤素取代(Cl、Br)的最高占据分子轨道(HOMO)-最低未占据分子轨道(LUMO)能隙。获得了温度范围为100 - 1000 K的统计热力学函数(热容、熵、振动配分函数和吉布斯自由能)。使用量子化学计算方法计算了极化率、第一超极化率、各向异性极化率不变量。还根据计算强度预测了红外光谱和拉曼光谱。实验光谱值与理论光谱值的比较提供了有关计算方法描述振动模式能力的重要信息。通过理论计算研究了TFMBP的紫外-可见光谱分析。为了理解该化合物的电子跃迁,进行了气相和溶剂(二甲基亚砜和氯仿)中电子吸收光谱的含时密度泛函理论(TD-DFT)计算。还展示了气相和溶剂(水和甲醇)中计算得到的前沿轨道能量、吸收波长(λ)、振子强度(ƒ)和激发能(E)。