Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane

Autores
Pinto da Silva, Luis; Ferreyra, Paulo J. O.; Duarte, Darío Jorge Roberto; Miranda, Margarida S.; Esteves da Silva, Joaquim C. G.
Año de publicación
2014
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The growing awareness of the harmful effects of ultraviolet (UV) solar radiation has increased the production and consumption of sunscreen products, which contain organic and inorganic molecules named UV filters that absorb, reflect, or scatter UV radiation, thus minimizing negative human health effects. 4-tert-Butyl-4′-methoxydibenzoylmethane (BMDBM) is one of the few organic UVA filters and the most commonly used. BMDBM exists in sunscreens in the enol form which absorbs strongly in the UVA range. However, under sunlight irradiation tautomerization occurs to the keto form, resulting in the loss of UV protection. In this study we have performed quantum chemical calculations to study the excited-state molecular structure and excitation spectra of the enol and keto tautomers of BMDBM. This knowledge is of the utmost importance as the starting point for studies aiming at the understanding of its activity when applied on human skin and also its fate once released into the aquatic environment. The efficiency of excitation transitions was rationalized based on the concept of molecular orbital superposition. The loss of UV protection was attributed to the enol → keto phototautomerism and subsequent photodegradation. Although this process is not energetically favorable in the singlet bright state, photodegradation is possible because of intersystem crossing to the first two triplet states.
Fil: Pinto da Silva, Luis . Universidade do Porto; Portugal
Fil: Ferreyra, Paulo J. O.. Universidade do Porto; Portugal
Fil: Duarte, Darío Jorge Roberto. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Miranda, Margarida S.. Universidade do Porto; Portugal
Fil: Esteves da Silva, Joaquim C. G.. Universidade do Porto; Portugal
Materia
4-Tert-Butyl-4`-Methoxydibenzoylmethane
Phototautomerism
Excited States
Uva Filters
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:11336/10224

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network_name_str CONICET Digital (CONICET)
spelling Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethanePinto da Silva, Luis Ferreyra, Paulo J. O.Duarte, Darío Jorge RobertoMiranda, Margarida S.Esteves da Silva, Joaquim C. G.4-Tert-Butyl-4`-MethoxydibenzoylmethanePhototautomerismExcited StatesUva Filtershttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The growing awareness of the harmful effects of ultraviolet (UV) solar radiation has increased the production and consumption of sunscreen products, which contain organic and inorganic molecules named UV filters that absorb, reflect, or scatter UV radiation, thus minimizing negative human health effects. 4-tert-Butyl-4′-methoxydibenzoylmethane (BMDBM) is one of the few organic UVA filters and the most commonly used. BMDBM exists in sunscreens in the enol form which absorbs strongly in the UVA range. However, under sunlight irradiation tautomerization occurs to the keto form, resulting in the loss of UV protection. In this study we have performed quantum chemical calculations to study the excited-state molecular structure and excitation spectra of the enol and keto tautomers of BMDBM. This knowledge is of the utmost importance as the starting point for studies aiming at the understanding of its activity when applied on human skin and also its fate once released into the aquatic environment. The efficiency of excitation transitions was rationalized based on the concept of molecular orbital superposition. The loss of UV protection was attributed to the enol → keto phototautomerism and subsequent photodegradation. Although this process is not energetically favorable in the singlet bright state, photodegradation is possible because of intersystem crossing to the first two triplet states.Fil: Pinto da Silva, Luis . Universidade do Porto; PortugalFil: Ferreyra, Paulo J. O.. Universidade do Porto; PortugalFil: Duarte, Darío Jorge Roberto. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Miranda, Margarida S.. Universidade do Porto; PortugalFil: Esteves da Silva, Joaquim C. G.. Universidade do Porto; PortugalAmerican Chemical Society2014-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/10224Pinto da Silva, Luis ; Ferreyra, Paulo J. O.; Duarte, Darío Jorge Roberto; Miranda, Margarida S.; Esteves da Silva, Joaquim C. G.; Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane; American Chemical Society; Journal Of Physical Chemistry A; 118; 8; 2-2014; 1511-15181089-5639enginfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021/jp4123375info:eu-repo/semantics/altIdentifier/doi/10.1021/jp4123375info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:10:53Zoai:ri.conicet.gov.ar:11336/10224instacron: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 10:10:53.414CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane
title Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane
spellingShingle Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane
Pinto da Silva, Luis
4-Tert-Butyl-4`-Methoxydibenzoylmethane
Phototautomerism
Excited States
Uva Filters
title_short Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane
title_full Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane
title_fullStr Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane
title_full_unstemmed Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane
title_sort Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane
dc.creator.none.fl_str_mv Pinto da Silva, Luis
Ferreyra, Paulo J. O.
Duarte, Darío Jorge Roberto
Miranda, Margarida S.
Esteves da Silva, Joaquim C. G.
author Pinto da Silva, Luis
author_facet Pinto da Silva, Luis
Ferreyra, Paulo J. O.
Duarte, Darío Jorge Roberto
Miranda, Margarida S.
Esteves da Silva, Joaquim C. G.
author_role author
author2 Ferreyra, Paulo J. O.
Duarte, Darío Jorge Roberto
Miranda, Margarida S.
Esteves da Silva, Joaquim C. G.
author2_role author
author
author
author
dc.subject.none.fl_str_mv 4-Tert-Butyl-4`-Methoxydibenzoylmethane
Phototautomerism
Excited States
Uva Filters
topic 4-Tert-Butyl-4`-Methoxydibenzoylmethane
Phototautomerism
Excited States
Uva Filters
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The growing awareness of the harmful effects of ultraviolet (UV) solar radiation has increased the production and consumption of sunscreen products, which contain organic and inorganic molecules named UV filters that absorb, reflect, or scatter UV radiation, thus minimizing negative human health effects. 4-tert-Butyl-4′-methoxydibenzoylmethane (BMDBM) is one of the few organic UVA filters and the most commonly used. BMDBM exists in sunscreens in the enol form which absorbs strongly in the UVA range. However, under sunlight irradiation tautomerization occurs to the keto form, resulting in the loss of UV protection. In this study we have performed quantum chemical calculations to study the excited-state molecular structure and excitation spectra of the enol and keto tautomers of BMDBM. This knowledge is of the utmost importance as the starting point for studies aiming at the understanding of its activity when applied on human skin and also its fate once released into the aquatic environment. The efficiency of excitation transitions was rationalized based on the concept of molecular orbital superposition. The loss of UV protection was attributed to the enol → keto phototautomerism and subsequent photodegradation. Although this process is not energetically favorable in the singlet bright state, photodegradation is possible because of intersystem crossing to the first two triplet states.
Fil: Pinto da Silva, Luis . Universidade do Porto; Portugal
Fil: Ferreyra, Paulo J. O.. Universidade do Porto; Portugal
Fil: Duarte, Darío Jorge Roberto. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Miranda, Margarida S.. Universidade do Porto; Portugal
Fil: Esteves da Silva, Joaquim C. G.. Universidade do Porto; Portugal
description The growing awareness of the harmful effects of ultraviolet (UV) solar radiation has increased the production and consumption of sunscreen products, which contain organic and inorganic molecules named UV filters that absorb, reflect, or scatter UV radiation, thus minimizing negative human health effects. 4-tert-Butyl-4′-methoxydibenzoylmethane (BMDBM) is one of the few organic UVA filters and the most commonly used. BMDBM exists in sunscreens in the enol form which absorbs strongly in the UVA range. However, under sunlight irradiation tautomerization occurs to the keto form, resulting in the loss of UV protection. In this study we have performed quantum chemical calculations to study the excited-state molecular structure and excitation spectra of the enol and keto tautomers of BMDBM. This knowledge is of the utmost importance as the starting point for studies aiming at the understanding of its activity when applied on human skin and also its fate once released into the aquatic environment. The efficiency of excitation transitions was rationalized based on the concept of molecular orbital superposition. The loss of UV protection was attributed to the enol → keto phototautomerism and subsequent photodegradation. Although this process is not energetically favorable in the singlet bright state, photodegradation is possible because of intersystem crossing to the first two triplet states.
publishDate 2014
dc.date.none.fl_str_mv 2014-02
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/11336/10224
Pinto da Silva, Luis ; Ferreyra, Paulo J. O.; Duarte, Darío Jorge Roberto; Miranda, Margarida S.; Esteves da Silva, Joaquim C. G.; Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane; American Chemical Society; Journal Of Physical Chemistry A; 118; 8; 2-2014; 1511-1518
1089-5639
url http://hdl.handle.net/11336/10224
identifier_str_mv Pinto da Silva, Luis ; Ferreyra, Paulo J. O.; Duarte, Darío Jorge Roberto; Miranda, Margarida S.; Esteves da Silva, Joaquim C. G.; Structural, Energetic, and UV−Vis Spectral Analysis of UVA Filter 4‑tert-Butyl-4′-methoxydibenzoylmethane; American Chemical Society; Journal Of Physical Chemistry A; 118; 8; 2-2014; 1511-1518
1089-5639
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/jp4123375
info:eu-repo/semantics/altIdentifier/doi/10.1021/jp4123375
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
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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