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Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/890

Title: From Sulfoxide Precursors to Model Oligomers of Conducting Polymers
Authors: Claes, L.
FRANCOIS, Jean-Pierre
DELEUZE, Michael
Issue Date: 2002
Publisher: ACS
Citation: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 124(25). p. 7563-7572
Abstract: The gas-phase internal elimination (Ei) reaction of the sulfoxide (-SO-CH3) precursors of ethylene and model oligomers of PPV and PITN has been investigated by means of Hartree-Fock, Mller-Plesset (second and fourth order), and Density Functional Theory (B3LYP, MPW1K) calculations. Considerable differences between the obtained ground state and transition state geometries and the calculated activation energies are observed from one approach to the other, justifying first a careful calibration against the results of a benchmark CCSD(T) study of the Ei reaction leading to ethylene. In comparison with the CCSD(T) results, as well as with available experimental data, DFT calculations along with the MPW1K functional are found to be a very appropriate choice for describing the Ei pathway. The leading conformations of the precursors, the relevant transition state structures, and the energy barriers encountered along the lowest energy path to unsubstituted, and chloro-, methoxy-, and cyano-substituted ethylene, styrene, stilbene in its cis and trans forms, and at last trans-biisothianaphthene have therefore been identified and characterized in detail employing DFT (MPW1K). Depending on the substituents attached to the C and C atoms, different reaction mechanisms are observed.
URI: http://hdl.handle.net/1942/890
DOI: 10.1021/ja012700p
ISI #: 000176338400050
ISSN: 0002-7863
Category: A1
Type: Journal Contribution
Validation: ecoom, 2003
Appears in Collections: Research publications

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