Theoretical spectroscopic signature of synephrine using DFT and the effect of hydrogen removal

• Published in: Phase transitions Vol. 95; no. 7; pp. 475 - 485
• Main Authors: Yadav, N. P., Vishwkarma, A. K., Kumar, K., Vats, A., Pathak, A., Kumar, R., Mukerjee, V., Moharana, S., Yadav, T., Mahapatra, C., Srivastava, S.
• Format: Journal Article
• Language: English
• Published: Abingdon Taylor & Francis 03.07.2022; Taylor & Francis Ltd
• Subjects: DFT; Electronic structure; Energy gap; Enthalpy; Mathematical analysis; Molecular orbitals; NBO; NCA; Optimization; Parameters; Radicals; Raman; Room temperature; Spectroscopy; Stability analysis; Structural stability; synephrine; Vapor phases
• ISSN: 0141-1594; 1029-0338
• DOI: 10.1080/01411594.2022.2085101

The present work deals with the vibrational spectroscopic signature of the synephrine molecule and its radical in the gas phase. We have optimized synephrine and synephrine - in the ground state. The optimization of the neutral and de-protonated synephrine has been performed at the B3LYP/6-31++G(d, p) level of theory. The comparison of vibrational frequencies of both the structures has also been made. Most of the vibrational frequencies are in good agreement with the experimental ones. The effect of hydrogen removal from the site of oxygen atom upon geometrical parameters and vibrational frequencies of synephrine has been reported. Subsequently, the different thermodynamical parameters calculated at room temperature for the synephrine and its radical have been discussed. Interestingly, the enthalpy of formation for the synephrine and deprotonated synephrine has been calculated. The NBO analysis has been performed to check the stability of the electronic structure of the radical form of the synephrine molecule. Also, the HOMO-LUMO energy gap infers that synephrine is more reactive in its radical form.