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Computational study of productive and non-productive cycles in fluoroalkene metathesis

A detailed DFT study of the mechanism of metathesis of fluoroethene, 1-fluoroethene, 1,1-difluoroethene, cis- and trans-1,2-difluoroethene, tetrafluoroethene and chlorotrifluoroethene catalysed with the Hoveyda–Grubbs 2(nd) generation catalyst was performed. It revealed that a successful metathesis...

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Autores principales: Rybáčková, Markéta, Hošek, Jan, Šimůnek, Ondřej, Kolaříková, Viola, Kvíčala, Jaroslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660995/
https://www.ncbi.nlm.nih.gov/pubmed/26664636
http://dx.doi.org/10.3762/bjoc.11.232
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author Rybáčková, Markéta
Hošek, Jan
Šimůnek, Ondřej
Kolaříková, Viola
Kvíčala, Jaroslav
author_facet Rybáčková, Markéta
Hošek, Jan
Šimůnek, Ondřej
Kolaříková, Viola
Kvíčala, Jaroslav
author_sort Rybáčková, Markéta
collection PubMed
description A detailed DFT study of the mechanism of metathesis of fluoroethene, 1-fluoroethene, 1,1-difluoroethene, cis- and trans-1,2-difluoroethene, tetrafluoroethene and chlorotrifluoroethene catalysed with the Hoveyda–Grubbs 2(nd) generation catalyst was performed. It revealed that a successful metathesis of hydrofluoroethenes is hampered by a high preference for a non-productive catalytic cycle proceeding through a ruthenacyclobutane intermediate bearing fluorines in positions 2 and 4. Moreover, the calculations showed that the cross-metathesis of perfluoro- or perhaloalkenes should be a feasible process and that the metathesis is not very sensitive to stereochemical issues.
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spelling pubmed-46609952015-12-09 Computational study of productive and non-productive cycles in fluoroalkene metathesis Rybáčková, Markéta Hošek, Jan Šimůnek, Ondřej Kolaříková, Viola Kvíčala, Jaroslav Beilstein J Org Chem Full Research Paper A detailed DFT study of the mechanism of metathesis of fluoroethene, 1-fluoroethene, 1,1-difluoroethene, cis- and trans-1,2-difluoroethene, tetrafluoroethene and chlorotrifluoroethene catalysed with the Hoveyda–Grubbs 2(nd) generation catalyst was performed. It revealed that a successful metathesis of hydrofluoroethenes is hampered by a high preference for a non-productive catalytic cycle proceeding through a ruthenacyclobutane intermediate bearing fluorines in positions 2 and 4. Moreover, the calculations showed that the cross-metathesis of perfluoro- or perhaloalkenes should be a feasible process and that the metathesis is not very sensitive to stereochemical issues. Beilstein-Institut 2015-11-10 /pmc/articles/PMC4660995/ /pubmed/26664636 http://dx.doi.org/10.3762/bjoc.11.232 Text en Copyright © 2015, Rybáčková et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Rybáčková, Markéta
Hošek, Jan
Šimůnek, Ondřej
Kolaříková, Viola
Kvíčala, Jaroslav
Computational study of productive and non-productive cycles in fluoroalkene metathesis
title Computational study of productive and non-productive cycles in fluoroalkene metathesis
title_full Computational study of productive and non-productive cycles in fluoroalkene metathesis
title_fullStr Computational study of productive and non-productive cycles in fluoroalkene metathesis
title_full_unstemmed Computational study of productive and non-productive cycles in fluoroalkene metathesis
title_short Computational study of productive and non-productive cycles in fluoroalkene metathesis
title_sort computational study of productive and non-productive cycles in fluoroalkene metathesis
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660995/
https://www.ncbi.nlm.nih.gov/pubmed/26664636
http://dx.doi.org/10.3762/bjoc.11.232
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