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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/22290
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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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1842270044816408576 |
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13.13397 |