Fast isomerizing methyl iodide azopyridinium salts for molecular switches
- Autores
- Garcia Amorós, Jaume; Massad, Walter Alfredo; Nonell, Santi; Velasco, Dolores
- Año de publicación
- 2010
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The usefulness of azopyridinium methyl iodide salts for designing new promising light-controlled molecular switches is presented. Large absorbance changes have been produced in the samples by irradiation with light at λ ) 355 nm. The thermal recovery of the initial state took place completely within 130-450 ms, which is much faster than that reported previously for other push-pull azobenzene-doped nematic mixtures.
Fil: Garcia Amorós, Jaume. Centro de Investigación en Nanociencia y Nanotecnología (CIN2); España. Universidad de Barcelona. Facultad de Química; España
Fil: Massad, Walter Alfredo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universitat Ramon Llull; España
Fil: Nonell, Santi. Universitat Ramon Llull; España
Fil: Velasco, Dolores. Centro de Investigación en Nanociencia y Nanotecnología (CIN2); España. Universidad de Barcelona. Facultad de Química; España - Materia
-
Azopyridinium salts
Molecular switches
Nematic mixtures - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/187564
Ver los metadatos del registro completo
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Fast isomerizing methyl iodide azopyridinium salts for molecular switchesGarcia Amorós, JaumeMassad, Walter AlfredoNonell, SantiVelasco, DoloresAzopyridinium saltsMolecular switchesNematic mixtureshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The usefulness of azopyridinium methyl iodide salts for designing new promising light-controlled molecular switches is presented. Large absorbance changes have been produced in the samples by irradiation with light at λ ) 355 nm. The thermal recovery of the initial state took place completely within 130-450 ms, which is much faster than that reported previously for other push-pull azobenzene-doped nematic mixtures.Fil: Garcia Amorós, Jaume. Centro de Investigación en Nanociencia y Nanotecnología (CIN2); España. Universidad de Barcelona. Facultad de Química; EspañaFil: Massad, Walter Alfredo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universitat Ramon Llull; EspañaFil: Nonell, Santi. Universitat Ramon Llull; EspañaFil: Velasco, Dolores. Centro de Investigación en Nanociencia y Nanotecnología (CIN2); España. Universidad de Barcelona. Facultad de Química; EspañaAmerican Chemical Society2010-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/187564Garcia Amorós, Jaume; Massad, Walter Alfredo; Nonell, Santi; Velasco, Dolores; Fast isomerizing methyl iodide azopyridinium salts for molecular switches; American Chemical Society; Organic Letters; 12; 15; 8-2010; 3514-35171523-70601523-7052CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/ol1013679info:eu-repo/semantics/altIdentifier/doi/10.1021/ol1013679info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-12T09:46:06Zoai:ri.conicet.gov.ar:11336/187564instacron: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:34982025-11-12 09:46:06.722CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Fast isomerizing methyl iodide azopyridinium salts for molecular switches |
| title |
Fast isomerizing methyl iodide azopyridinium salts for molecular switches |
| spellingShingle |
Fast isomerizing methyl iodide azopyridinium salts for molecular switches Garcia Amorós, Jaume Azopyridinium salts Molecular switches Nematic mixtures |
| title_short |
Fast isomerizing methyl iodide azopyridinium salts for molecular switches |
| title_full |
Fast isomerizing methyl iodide azopyridinium salts for molecular switches |
| title_fullStr |
Fast isomerizing methyl iodide azopyridinium salts for molecular switches |
| title_full_unstemmed |
Fast isomerizing methyl iodide azopyridinium salts for molecular switches |
| title_sort |
Fast isomerizing methyl iodide azopyridinium salts for molecular switches |
| dc.creator.none.fl_str_mv |
Garcia Amorós, Jaume Massad, Walter Alfredo Nonell, Santi Velasco, Dolores |
| author |
Garcia Amorós, Jaume |
| author_facet |
Garcia Amorós, Jaume Massad, Walter Alfredo Nonell, Santi Velasco, Dolores |
| author_role |
author |
| author2 |
Massad, Walter Alfredo Nonell, Santi Velasco, Dolores |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
Azopyridinium salts Molecular switches Nematic mixtures |
| topic |
Azopyridinium salts Molecular switches Nematic mixtures |
| 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 usefulness of azopyridinium methyl iodide salts for designing new promising light-controlled molecular switches is presented. Large absorbance changes have been produced in the samples by irradiation with light at λ ) 355 nm. The thermal recovery of the initial state took place completely within 130-450 ms, which is much faster than that reported previously for other push-pull azobenzene-doped nematic mixtures. Fil: Garcia Amorós, Jaume. Centro de Investigación en Nanociencia y Nanotecnología (CIN2); España. Universidad de Barcelona. Facultad de Química; España Fil: Massad, Walter Alfredo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universitat Ramon Llull; España Fil: Nonell, Santi. Universitat Ramon Llull; España Fil: Velasco, Dolores. Centro de Investigación en Nanociencia y Nanotecnología (CIN2); España. Universidad de Barcelona. Facultad de Química; España |
| description |
The usefulness of azopyridinium methyl iodide salts for designing new promising light-controlled molecular switches is presented. Large absorbance changes have been produced in the samples by irradiation with light at λ ) 355 nm. The thermal recovery of the initial state took place completely within 130-450 ms, which is much faster than that reported previously for other push-pull azobenzene-doped nematic mixtures. |
| publishDate |
2010 |
| dc.date.none.fl_str_mv |
2010-08 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/187564 Garcia Amorós, Jaume; Massad, Walter Alfredo; Nonell, Santi; Velasco, Dolores; Fast isomerizing methyl iodide azopyridinium salts for molecular switches; American Chemical Society; Organic Letters; 12; 15; 8-2010; 3514-3517 1523-7060 1523-7052 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/187564 |
| identifier_str_mv |
Garcia Amorós, Jaume; Massad, Walter Alfredo; Nonell, Santi; Velasco, Dolores; Fast isomerizing methyl iodide azopyridinium salts for molecular switches; American Chemical Society; Organic Letters; 12; 15; 8-2010; 3514-3517 1523-7060 1523-7052 CONICET Digital CONICET |
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eng |
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eng |
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openAccess |
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American Chemical Society |
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American Chemical Society |
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