dc.creatorAcevedo, R.
dc.creatorVasquez, S. O.
dc.creatorFlint, C. D.
dc.date.accessioned2018-12-20T14:35:49Z
dc.date.available2018-12-20T14:35:49Z
dc.date.created2018-12-20T14:35:49Z
dc.date.issued1991
dc.identifierMolecular Physics, Volumen 74, Issue 4, 2018, Pages 853-860
dc.identifier13623028
dc.identifier00268976
dc.identifier10.1080/00268979100102631
dc.identifierhttps://repositorio.uchile.cl/handle/2250/156591
dc.description.abstractA method to estimate the contribution to the vibronic intensity in electronic transitions of inorganic complex ions due to second order terms in the Herzberg-Teller expansion of vibronic wavefunctions is developed and applied to the 4A2g ↔ 4T2g transition of the MnF2- 6 ion. Both crystal field and ligand polarization contributions are derived, the crystal field term being evaluated in the single intermediate p state approximation. Contributions to the intensity of the nine second order terms are evaluated for several force fields and compared with recent experimental data. Although there are some difficulties in this comparison, it provides some support both for the model and the attribution of the intensity mechanism. © 1991 Taylor and Francis Group, LLC.
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceMolecular Physics
dc.subjectBiophysics
dc.subjectMolecular Biology
dc.subjectPhysical and Theoretical Chemistry
dc.subjectCondensed Matter Physics
dc.titleVibronic intensities in the electronic spectra of transition metal complex ions. part x. second order herzberg-teller contributions to the vibronic intensity of the 4A2g ↔ 4T2g transition in MnF 2- 6
dc.typeArtículo de revista


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