Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/4546
Title: Solvent effects on 2-methoxyethanol conformers: an ab initio DFT study using the SCI-PCModel
Authors: Gil, Francisco P. S. C. 
Teixeira-Dias, J. J. C. 
Keywords: 2-methoxyethanol; solvent effects; Self-Consistent Reaction Field (SCRF); Self-Consistent Isodensity Polarizable Continuum Model (SCI-PCM)
Issue Date: 1999
Citation: Journal of Molecular Structure. 482-483:(1999) 621-625
Abstract: The four stable conformers of 2-methoxyethanol, CH3O-CH2-CH2-OH (tgg', ggg', ttg and ttt) are studied by ab initio calculations using the SCRF theory and the SCI-PCModel to assess solvent effects on the structure and vibrational spectra of this compound. Full geometry optimizations were carried out at the B3LYP/6-311+G(3df,2df,2p)//B3LYP/6-31G(d) level, and normal mode calculations were performed within the harmonic approximation using the B3LYP/6-31G(d) derived force fields. The solvent, herein represented by a polarizable continuum with a defined dielectric constant, is found to affect significantly the geometry and dipole moment of the individual solute conformers. In addition, the results seem to suggest that the intramolecular H-bond type of interactions, which occur for tgg' and ggg', tend to attenuate the solvent influence. In turn, the conformers which do not exhibit intramolecular H-bond interactions, ttg and ttt, exhibit a stronger solvent influence as revealed mainly by structural and electrostatic changes affecting both the ether O atom and the hydroxyl group.
URI: http://hdl.handle.net/10316/4546
Rights: openAccess
Appears in Collections:FCTUC Física - Artigos em Revistas Internacionais

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