The conformation and ring-puckering vibration of 2-methyloxetane from microwave spectroscopy and ab initio computations
| Autor: | JoséL. Alonso, T. Eggimann, M.E. Charro, David G. Lister, J. C. Lopez, H. Wieser |
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| Rok vydání: | 1993 |
| Předmět: |
Chemistry
General Physics and Astronomy Rotational–vibrational spectroscopy Energy minimization Molecular physics symbols.namesake Electric dipole moment Atomic orbital Far infrared Stark effect Computational chemistry Excited state symbols Rotational spectroscopy Physics::Chemical Physics Physical and Theoretical Chemistry |
| Zdroj: | Chemical Physics. 172:303-314 |
| ISSN: | 0301-0104 |
| DOI: | 10.1016/0301-0104(93)80125-s |
| Popis: | The conformation and ring-puckering vibration of 2-methoxyloxetane have been studied using microwave spectroscopy and ab initio computations. The microwave spectra of the ground and first four excited states of the ring-puckering vibration have been observed in the frequency range 8–40 GHz and the rotational and quadratic centrifugal distortion constants have been determined. Vibrational energy separations have been obtained from relative intensity measurements. The electric dipole moment (in D) of the ground vibrational state has been determined from Stark effect measurements as μ a = 0.0187 (5), μ b = 1.852 (2), μ c = 0.08 (3), and μ t = 1.854 (3). The vibrational energy separations and the vibrational dependence of the rotational constants suggest that the ring-puckering vibrational has an asymmetric single minimum potential function and also gave a revised assignment of the far infrared spectrum (J. Mol. Struct. 56 (1979) 157). A combined fit to the rotational constants, vibrational energy separations and far infrared vibrational frequencies has been used to determine a reduced potential for the ring puckering vibration. The partial derivatives of the rotational constants with respect to the reduced ring-puckering coordinate show that the equilibrium conformation has the methyl group in the equatorial position. Ab initio computations of the ring-puckering potential function have been made using 6-31G * orbitals and full geometry optimization. These computations also show the molecule to have an asymmetric single minimum potential function with an equatorial equilibrium conformation. |
| Databáze: | OpenAIRE |
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