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From the same journal

Gas-phase structure, rotational barrier and vibrational properties of trimethylsilyl trifluoroacetate CF3C(O)OSi(CH3) 3: An experimental and computational study

Research output: Contribution to journalArticle

Author(s)

  • M.E. Defonsi Lestard
  • M.E. Tuttolomondo
  • E.L. Varetti
  • D.A. Wann
  • H.E. Robertson
  • D.W.H. Rankin
  • A. Ben Altabef

Department/unit(s)

Publication details

JournalJOURNAL OF MOLECULAR STRUCTURE
DatePublished - 20 Aug 2010
Issue number1-3
Volume978
Number of pages10
Pages (from-to)114-123
Original languageUndefined/Unknown

Abstract

The molecular structure of trimethylsilyl trifluoroacetate, CF 3C(O)OSi(CH3)3, has been determined in the gas phase from electron-diffraction data supplemented by ab initio (MP2) and DFT calculations using 6-31G(d), 6-311G(d,p), 6-311++G(d,p) and 6-311++G(3df,3pd) basis sets. Experimental data indicate that only one conformer, with C s symmetry [dihedral angle φ(CCOSi) = 180°, and all groups staggered], is observed in the gas phase. Theoretical data indicate that both this anti conformer and a gauche conformer, created by rotating about the C(O)O bond, are possible, although the preferred conformation is the staggered anti one. The torsional energies for different values of the CCOSi and COSiC dihedral angles have been calculated using the RHF, MP2 and B3LYP methods with the 6-311++G(d,p) basis set. For rotation around the CCOSi bond, a sixfold decomposition of the rotational barrier has been performed in terms of a Fourier-type expansion, enabling us to analyze the nature of the potential function, showing that the coefficients related to electrostatic interactions and steric effects are the dominant terms. The preference for the anti conformation was studied using the total-energy scheme, comparison of dipole moments, and the natural bond orbital partition scheme. The infrared spectra for the liquid and gas phases and the Raman spectrum for the liquid phase have also been recorded and the observed bands assigned to the vibrational normal modes. The experimental vibrational data, along with calculated theoretical force constants, were used to define a scaled quantum mechanical force field for the target system that enabled us to estimate the measured frequencies with a final root-mean-square deviation of 9.7 cm-1. © 2010 Elsevier B.V. All rights reserved.

Bibliographical note

Cited By (since 1996):1

Export Date: 1 October 2013

Source: Scopus

CODEN: JMOSB

doi: 10.1016/j.molstruc.2010.02.046

Language of Original Document: English

Correspondence Address: Ben Altabef, A.; INQUINOA, CONICET, Universidad Nacional de Tucumán, San Lorenzo 456, T4000CAN Tucumán, Argentina; email: altabef@fbqf.unt.edu.ar

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    Research areas

  • Ab initio, DFT, GED, NBO, Anti conformers, Anti-conformations, B3LYP method, Basis sets, Computational studies, DFT calculation, Dihedral angles, Electron diffraction data, Electrostatic interactions, Energy schemes, Experimental data, Force constants, Fourier, Gas-phase structures, Gasphase, Gauche conformer, Infrared spectrum, Liquid and gas phasis, Liquid Phase, Natural bond orbital, Partition schemes, Potential function, Raman Spectrum, Root-mean square deviation, Rotational barriers, Scaled quantum mechanical force fields, Steric effect, Target systems, Torsional energies, Trifluoroacetates, Trimethylsilyl, Vibrational normal modes, Vibrational properties, Conformations, Liquids, Quantum theory, Raman spectroscopy, Rotation, Gases

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