Conformational changes of an oxovanadium complex probed by ENDOR spectroscopy and DFT calculations

Murphy, Damien Martin ORCID: https://orcid.org/0000-0002-5941-4879, Fallis, Ian Andrew ORCID: https://orcid.org/0000-0001-7361-0182, Farley, Robert Dexter, Tucker, Richard J., Avery, Karen L. and Willock, David James ORCID: https://orcid.org/0000-0002-8893-1090 2002. Conformational changes of an oxovanadium complex probed by ENDOR spectroscopy and DFT calculations. Physical Chemistry Chemical Physics 4 (20) , pp. 4937-4943. 10.1039/b204564h

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Abstract

An angular selective ENDOR study, in combination with DFT calculations, was used to investigate the structure and conformational changes of the bis(acetylacetonato)-oxovanadium(IV) complex ([VIVO(acac)2]) in frozen solution. In the presence of a non-coordinating solvent (dichloromethane), both ENDOR analysis and DFT calculations confirm the expected square pyramidal structure of the complex. However, when a strongly coordinating solvent (d5-pyridine) was used, different structural isomers of the resulting ([VIVO(acac)2(C5D5N)]) adduct were found to co-exist in the frozen solution. ENDOR simulations indicate that 60% of the adduct is present as the cis-isomer, while 40% is present as the trans-isomer. The ligand coordinates of both isomers, as determined by ENDOR spectroscopy, were in excellent agreement with the optimised structure based on DFT calculations. In addition, the DFT calculations showed that the total energy of the two isomers for the pyridine case differ by only 3 kJ mol−1, in agreement with the experimentally observed equilibrium mixture containing both isomers.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Chemistry Cardiff Catalysis Institute (CCI)
Subjects:	Q Science > QD Chemistry
Publisher:	Royal Society of Chemistry
ISSN:	1463-9076
Last Modified:	17 Oct 2022 08:54
URI:	https://orca.cardiff.ac.uk/id/eprint/1401

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