Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes
- Autores
- Cadranel, Alejandro; Oviedo, Paola Soledad; Pieslinger, German Eduardo; Yamazaki, Shiori; Kleiman, Valeria D.; Baraldo Victorica, Luis Mario; Guldi, Dirk M.
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The picosecond excited state dynamics of [Ru(tpm)(bpy)(NCS)]+ (RubNCS+) and [Ru(tpm)(bpy)(CN)]+ (RubCN+) (tpm = tris(1-pyrazolyl)methane, bpy = 2,2′-bipyridine) have been analyzed by means of transient absorption measurements and spectroelectrochemistry. Emissive 3MLCTs with (GS)HOMO(h+)-(GS)LUMO(e-) configurations are the lowest triplet excited states regardless of whether 387 or 505 nm photoexcitation is used. 387 nm photoexcitation yields, after a few picoseconds, the emissive 3MLCTs. In contrast, 505 nm photoexcitation populates an intermediate excited state that we assign as a 3MLCT state, in which the hole sits in a metal-centered orbital of different symmetry, prior to its conversion to the emissive 3MLCTs. The disparities in terms of electronic configuration between the intermediate and the emissive 3MLCTs have two important consequences. On one hand, both states feature very different fingerprint absorptions in transient absorption measurements. On the other hand, the reconfiguration is impeded by a kinetic barrier. As such, the conversion is followed spectroscopically and kinetically on the 300 ps timescale.
Fil: Cadranel, Alejandro. Universitat Erlangen-Nuremberg; Alemania
Fil: Oviedo, Paola Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Pieslinger, German Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Yamazaki, Shiori. University of Florida. Departament of Chemistry; Estados Unidos
Fil: Kleiman, Valeria D.. University of Florida. Departament of Chemistry; Estados Unidos
Fil: Baraldo Victorica, Luis Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Guldi, Dirk M.. Universitat Erlangen-Nuremberg; Alemania - Materia
-
Ruthenium Polypyridines
MLCT Excited State - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/65758
Ver los metadatos del registro completo
| id |
CONICETDig_5ba91215bfe6855e2215c207f7bc3fa4 |
|---|---|
| oai_identifier_str |
oai:ri.conicet.gov.ar:11336/65758 |
| network_acronym_str |
CONICETDig |
| repository_id_str |
3498 |
| network_name_str |
CONICET Digital (CONICET) |
| spelling |
Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexesCadranel, AlejandroOviedo, Paola SoledadPieslinger, German EduardoYamazaki, ShioriKleiman, Valeria D.Baraldo Victorica, Luis MarioGuldi, Dirk M.Ruthenium PolypyridinesMLCT Excited Statehttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The picosecond excited state dynamics of [Ru(tpm)(bpy)(NCS)]+ (RubNCS+) and [Ru(tpm)(bpy)(CN)]+ (RubCN+) (tpm = tris(1-pyrazolyl)methane, bpy = 2,2′-bipyridine) have been analyzed by means of transient absorption measurements and spectroelectrochemistry. Emissive 3MLCTs with (GS)HOMO(h+)-(GS)LUMO(e-) configurations are the lowest triplet excited states regardless of whether 387 or 505 nm photoexcitation is used. 387 nm photoexcitation yields, after a few picoseconds, the emissive 3MLCTs. In contrast, 505 nm photoexcitation populates an intermediate excited state that we assign as a 3MLCT state, in which the hole sits in a metal-centered orbital of different symmetry, prior to its conversion to the emissive 3MLCTs. The disparities in terms of electronic configuration between the intermediate and the emissive 3MLCTs have two important consequences. On one hand, both states feature very different fingerprint absorptions in transient absorption measurements. On the other hand, the reconfiguration is impeded by a kinetic barrier. As such, the conversion is followed spectroscopically and kinetically on the 300 ps timescale.Fil: Cadranel, Alejandro. Universitat Erlangen-Nuremberg; AlemaniaFil: Oviedo, Paola Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Pieslinger, German Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Yamazaki, Shiori. University of Florida. Departament of Chemistry; Estados UnidosFil: Kleiman, Valeria D.. University of Florida. Departament of Chemistry; Estados UnidosFil: Baraldo Victorica, Luis Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Guldi, Dirk M.. Universitat Erlangen-Nuremberg; AlemaniaRoyal Society of Chemistry2017-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/65758Cadranel, Alejandro; Oviedo, Paola Soledad; Pieslinger, German Eduardo; Yamazaki, Shiori; Kleiman, Valeria D.; et al.; Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes; Royal Society of Chemistry; Chemical Science; 8; 11; 8-2017; 7434-74422041-65202041-6539CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://xlink.rsc.org/?DOI=C7SC02670Finfo:eu-repo/semantics/altIdentifier/doi/10.1039/C7SC02670Finfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-05T09:44:10Zoai:ri.conicet.gov.ar:11336/65758instacron: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:34982025-11-05 09:44:10.993CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes |
| title |
Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes |
| spellingShingle |
Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes Cadranel, Alejandro Ruthenium Polypyridines MLCT Excited State |
| title_short |
Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes |
| title_full |
Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes |
| title_fullStr |
Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes |
| title_full_unstemmed |
Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes |
| title_sort |
Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes |
| dc.creator.none.fl_str_mv |
Cadranel, Alejandro Oviedo, Paola Soledad Pieslinger, German Eduardo Yamazaki, Shiori Kleiman, Valeria D. Baraldo Victorica, Luis Mario Guldi, Dirk M. |
| author |
Cadranel, Alejandro |
| author_facet |
Cadranel, Alejandro Oviedo, Paola Soledad Pieslinger, German Eduardo Yamazaki, Shiori Kleiman, Valeria D. Baraldo Victorica, Luis Mario Guldi, Dirk M. |
| author_role |
author |
| author2 |
Oviedo, Paola Soledad Pieslinger, German Eduardo Yamazaki, Shiori Kleiman, Valeria D. Baraldo Victorica, Luis Mario Guldi, Dirk M. |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
Ruthenium Polypyridines MLCT Excited State |
| topic |
Ruthenium Polypyridines MLCT Excited State |
| 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 picosecond excited state dynamics of [Ru(tpm)(bpy)(NCS)]+ (RubNCS+) and [Ru(tpm)(bpy)(CN)]+ (RubCN+) (tpm = tris(1-pyrazolyl)methane, bpy = 2,2′-bipyridine) have been analyzed by means of transient absorption measurements and spectroelectrochemistry. Emissive 3MLCTs with (GS)HOMO(h+)-(GS)LUMO(e-) configurations are the lowest triplet excited states regardless of whether 387 or 505 nm photoexcitation is used. 387 nm photoexcitation yields, after a few picoseconds, the emissive 3MLCTs. In contrast, 505 nm photoexcitation populates an intermediate excited state that we assign as a 3MLCT state, in which the hole sits in a metal-centered orbital of different symmetry, prior to its conversion to the emissive 3MLCTs. The disparities in terms of electronic configuration between the intermediate and the emissive 3MLCTs have two important consequences. On one hand, both states feature very different fingerprint absorptions in transient absorption measurements. On the other hand, the reconfiguration is impeded by a kinetic barrier. As such, the conversion is followed spectroscopically and kinetically on the 300 ps timescale. Fil: Cadranel, Alejandro. Universitat Erlangen-Nuremberg; Alemania Fil: Oviedo, Paola Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Pieslinger, German Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Yamazaki, Shiori. University of Florida. Departament of Chemistry; Estados Unidos Fil: Kleiman, Valeria D.. University of Florida. Departament of Chemistry; Estados Unidos Fil: Baraldo Victorica, Luis Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Guldi, Dirk M.. Universitat Erlangen-Nuremberg; Alemania |
| description |
The picosecond excited state dynamics of [Ru(tpm)(bpy)(NCS)]+ (RubNCS+) and [Ru(tpm)(bpy)(CN)]+ (RubCN+) (tpm = tris(1-pyrazolyl)methane, bpy = 2,2′-bipyridine) have been analyzed by means of transient absorption measurements and spectroelectrochemistry. Emissive 3MLCTs with (GS)HOMO(h+)-(GS)LUMO(e-) configurations are the lowest triplet excited states regardless of whether 387 or 505 nm photoexcitation is used. 387 nm photoexcitation yields, after a few picoseconds, the emissive 3MLCTs. In contrast, 505 nm photoexcitation populates an intermediate excited state that we assign as a 3MLCT state, in which the hole sits in a metal-centered orbital of different symmetry, prior to its conversion to the emissive 3MLCTs. The disparities in terms of electronic configuration between the intermediate and the emissive 3MLCTs have two important consequences. On one hand, both states feature very different fingerprint absorptions in transient absorption measurements. On the other hand, the reconfiguration is impeded by a kinetic barrier. As such, the conversion is followed spectroscopically and kinetically on the 300 ps timescale. |
| publishDate |
2017 |
| dc.date.none.fl_str_mv |
2017-08 |
| 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/11336/65758 Cadranel, Alejandro; Oviedo, Paola Soledad; Pieslinger, German Eduardo; Yamazaki, Shiori; Kleiman, Valeria D.; et al.; Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes; Royal Society of Chemistry; Chemical Science; 8; 11; 8-2017; 7434-7442 2041-6520 2041-6539 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/65758 |
| identifier_str_mv |
Cadranel, Alejandro; Oviedo, Paola Soledad; Pieslinger, German Eduardo; Yamazaki, Shiori; Kleiman, Valeria D.; et al.; Trapping intermediate MLCT states in low-symmetry {Ru(bpy)} complexes; Royal Society of Chemistry; Chemical Science; 8; 11; 8-2017; 7434-7442 2041-6520 2041-6539 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://xlink.rsc.org/?DOI=C7SC02670F info:eu-repo/semantics/altIdentifier/doi/10.1039/C7SC02670F |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by/2.5/ar/ |
| eu_rights_str_mv |
openAccess |
| rights_invalid_str_mv |
https://creativecommons.org/licenses/by/2.5/ar/ |
| dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf application/pdf application/pdf |
| dc.publisher.none.fl_str_mv |
Royal Society of Chemistry |
| publisher.none.fl_str_mv |
Royal Society of Chemistry |
| 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 |
| _version_ |
1847977046630727680 |
| score |
13.121305 |