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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/10224
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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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1842270136007917568 |
score |
13.13397 |