Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers

Autores
Provasi, Patricio Federico; Aucar, Gustavo Adolfo; Sauer, Stephan P. A.
Año de publicación
2004
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Large long-range indirect nuclear spin coupling constants are of great interest for quantum computers. But they are rarely observed and are usually considered very small, unless the coupled nuclear spins are proximate in space. Looking for counterexamples, we have calculated F−F couplings in four different series of acyclic hydrocarbons (alkanes, conjugated polyenes, conjugated polyynes, and cumulenes) where the coupled fluorine nuclei are separated by up to 11 bonds or 1.4 nm. The calculations were carried out at the level of the second-order polarization propagator approximation using locally dense basis sets. This approach has, in recent years, been shown to be particularly successful in reproducing indirect nuclear spin−spin couplings in organic molecules. We find that the F−F couplings in saturated alkanes diminish very quickly with the number of bonds between the coupled fluorine atoms, whereas in the conjugated polyenes and in particular polyynes the F−F couplings can be transmitted over much longer distances. We predict that the F−F coupling over 9 bonds or 1.1 nm is 12 Hz in (1E,3E,5E,7E)-1,8-difluoroocta-1,3,5,7-tetraene and the coupling over 11 bonds or 1.4 nm is 7 Hz in difluorodecapentayne. Analyzing the four Ramsey contributions, we find that the F−F couplings in the polyenes are dominated by the spin−dipolar term, which is known to be favored by π-electronic systems, whereas in the case of the polyynes the orbital paramagnetic terms make the largest contributions, although the spin−dipolar and the Fermi contact contributions are also significant.
Fil: Provasi, Patricio Federico. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura. Departamento de Física; Argentina
Fil: Aucar, Gustavo Adolfo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura. Departamento de Física; Argentina
Fil: Sauer, Stephan P. A.. Universidad de Copenhagen; Dinamarca
Materia
Nmr
Spin-Spin Coupling Constant
Long Range Coupling Constant
Fluorine-Fluorine
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/22290

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spelling Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometersProvasi, Patricio FedericoAucar, Gustavo AdolfoSauer, Stephan P. A.NmrSpin-Spin Coupling ConstantLong Range Coupling ConstantFluorine-Fluorinehttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1Large long-range indirect nuclear spin coupling constants are of great interest for quantum computers. But they are rarely observed and are usually considered very small, unless the coupled nuclear spins are proximate in space. Looking for counterexamples, we have calculated F−F couplings in four different series of acyclic hydrocarbons (alkanes, conjugated polyenes, conjugated polyynes, and cumulenes) where the coupled fluorine nuclei are separated by up to 11 bonds or 1.4 nm. The calculations were carried out at the level of the second-order polarization propagator approximation using locally dense basis sets. This approach has, in recent years, been shown to be particularly successful in reproducing indirect nuclear spin−spin couplings in organic molecules. We find that the F−F couplings in saturated alkanes diminish very quickly with the number of bonds between the coupled fluorine atoms, whereas in the conjugated polyenes and in particular polyynes the F−F couplings can be transmitted over much longer distances. We predict that the F−F coupling over 9 bonds or 1.1 nm is 12 Hz in (1E,3E,5E,7E)-1,8-difluoroocta-1,3,5,7-tetraene and the coupling over 11 bonds or 1.4 nm is 7 Hz in difluorodecapentayne. Analyzing the four Ramsey contributions, we find that the F−F couplings in the polyenes are dominated by the spin−dipolar term, which is known to be favored by π-electronic systems, whereas in the case of the polyynes the orbital paramagnetic terms make the largest contributions, although the spin−dipolar and the Fermi contact contributions are also significant.Fil: Provasi, Patricio Federico. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura. Departamento de Física; ArgentinaFil: Aucar, Gustavo Adolfo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura. Departamento de Física; ArgentinaFil: Sauer, Stephan P. A.. Universidad de Copenhagen; DinamarcaAmerican Chemical Society2004-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/22290Provasi, Patricio Federico; Aucar, Gustavo Adolfo; Sauer, Stephan P. A.; Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers; American Chemical Society; Journal of Physical Chemistry A; 108; 25; 5-2004; 5393-53981089-56391520-5215CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021%2Fjp048686vinfo:eu-repo/semantics/altIdentifier/doi/10.1021/jp048686vinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:08:26Zoai:ri.conicet.gov.ar:11336/22290instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:08:26.613CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers
title Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers
spellingShingle Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers
Provasi, Patricio Federico
Nmr
Spin-Spin Coupling Constant
Long Range Coupling Constant
Fluorine-Fluorine
title_short Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers
title_full Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers
title_fullStr Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers
title_full_unstemmed Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers
title_sort Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers
dc.creator.none.fl_str_mv Provasi, Patricio Federico
Aucar, Gustavo Adolfo
Sauer, Stephan P. A.
author Provasi, Patricio Federico
author_facet Provasi, Patricio Federico
Aucar, Gustavo Adolfo
Sauer, Stephan P. A.
author_role author
author2 Aucar, Gustavo Adolfo
Sauer, Stephan P. A.
author2_role author
author
dc.subject.none.fl_str_mv Nmr
Spin-Spin Coupling Constant
Long Range Coupling Constant
Fluorine-Fluorine
topic Nmr
Spin-Spin Coupling Constant
Long Range Coupling Constant
Fluorine-Fluorine
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.3
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Large long-range indirect nuclear spin coupling constants are of great interest for quantum computers. But they are rarely observed and are usually considered very small, unless the coupled nuclear spins are proximate in space. Looking for counterexamples, we have calculated F−F couplings in four different series of acyclic hydrocarbons (alkanes, conjugated polyenes, conjugated polyynes, and cumulenes) where the coupled fluorine nuclei are separated by up to 11 bonds or 1.4 nm. The calculations were carried out at the level of the second-order polarization propagator approximation using locally dense basis sets. This approach has, in recent years, been shown to be particularly successful in reproducing indirect nuclear spin−spin couplings in organic molecules. We find that the F−F couplings in saturated alkanes diminish very quickly with the number of bonds between the coupled fluorine atoms, whereas in the conjugated polyenes and in particular polyynes the F−F couplings can be transmitted over much longer distances. We predict that the F−F coupling over 9 bonds or 1.1 nm is 12 Hz in (1E,3E,5E,7E)-1,8-difluoroocta-1,3,5,7-tetraene and the coupling over 11 bonds or 1.4 nm is 7 Hz in difluorodecapentayne. Analyzing the four Ramsey contributions, we find that the F−F couplings in the polyenes are dominated by the spin−dipolar term, which is known to be favored by π-electronic systems, whereas in the case of the polyynes the orbital paramagnetic terms make the largest contributions, although the spin−dipolar and the Fermi contact contributions are also significant.
Fil: Provasi, Patricio Federico. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura. Departamento de Física; Argentina
Fil: Aucar, Gustavo Adolfo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura. Departamento de Física; Argentina
Fil: Sauer, Stephan P. A.. Universidad de Copenhagen; Dinamarca
description Large long-range indirect nuclear spin coupling constants are of great interest for quantum computers. But they are rarely observed and are usually considered very small, unless the coupled nuclear spins are proximate in space. Looking for counterexamples, we have calculated F−F couplings in four different series of acyclic hydrocarbons (alkanes, conjugated polyenes, conjugated polyynes, and cumulenes) where the coupled fluorine nuclei are separated by up to 11 bonds or 1.4 nm. The calculations were carried out at the level of the second-order polarization propagator approximation using locally dense basis sets. This approach has, in recent years, been shown to be particularly successful in reproducing indirect nuclear spin−spin couplings in organic molecules. We find that the F−F couplings in saturated alkanes diminish very quickly with the number of bonds between the coupled fluorine atoms, whereas in the conjugated polyenes and in particular polyynes the F−F couplings can be transmitted over much longer distances. We predict that the F−F coupling over 9 bonds or 1.1 nm is 12 Hz in (1E,3E,5E,7E)-1,8-difluoroocta-1,3,5,7-tetraene and the coupling over 11 bonds or 1.4 nm is 7 Hz in difluorodecapentayne. Analyzing the four Ramsey contributions, we find that the F−F couplings in the polyenes are dominated by the spin−dipolar term, which is known to be favored by π-electronic systems, whereas in the case of the polyynes the orbital paramagnetic terms make the largest contributions, although the spin−dipolar and the Fermi contact contributions are also significant.
publishDate 2004
dc.date.none.fl_str_mv 2004-05
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/22290
Provasi, Patricio Federico; Aucar, Gustavo Adolfo; Sauer, Stephan P. A.; Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers; American Chemical Society; Journal of Physical Chemistry A; 108; 25; 5-2004; 5393-5398
1089-5639
1520-5215
CONICET Digital
CONICET
url http://hdl.handle.net/11336/22290
identifier_str_mv Provasi, Patricio Federico; Aucar, Gustavo Adolfo; Sauer, Stephan P. A.; Large long-range F-F indirect spin-spin coupling constants. Prediction of measurable F-F couplings over a few nanometers; American Chemical Society; Journal of Physical Chemistry A; 108; 25; 5-2004; 5393-5398
1089-5639
1520-5215
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021%2Fjp048686v
info:eu-repo/semantics/altIdentifier/doi/10.1021/jp048686v
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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