Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative
The UV irradiation of a hexane solution of the complex (h5 -C5Me4(CH2)2NMe2)Re(CO)3 (1) afforded the chelated species (h5 :h1 -C5Me4(CH2)2NMe2)Re(CO)2 (2). The molecular structure of 2 has been determined by X-ray crystallography. The reaction of 2 with two-electron donor ligands yields (h5 - C5Me4(...
| Autores: | , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2014 |
| País: | Argentina |
| Institución: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositorio: | CONICET Digital (CONICET) |
| Idioma: | inglés |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/31816 |
| Acceso en línea: | http://hdl.handle.net/11336/31816 |
| Access Level: | acceso abierto |
| Palabra clave: | Rhenium Nitrosyl Cyclopentadienyl Functionalized https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
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| dc.title.none.fl_str_mv |
Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative |
| title |
Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative |
| spellingShingle |
Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative Godoy, Fernando Rhenium Nitrosyl Cyclopentadienyl Functionalized https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| title_short |
Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative |
| title_full |
Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative |
| title_fullStr |
Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative |
| title_full_unstemmed |
Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative |
| title_sort |
Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative |
| dc.creator.none.fl_str_mv |
Godoy, Fernando Gómez, Alejandra Segura, Rodrigo Doctorovich, Fabio Pellegrino, Juan Gaviglio, Carina del Valle Guerrero, Paulina Klahn, A. Hugo Fuentealba, Mauricio Garland, María Teresa |
| author |
Godoy, Fernando |
| author_facet |
Godoy, Fernando Gómez, Alejandra Segura, Rodrigo Doctorovich, Fabio Pellegrino, Juan Gaviglio, Carina del Valle Guerrero, Paulina Klahn, A. Hugo Fuentealba, Mauricio Garland, María Teresa |
| author_role |
author |
| author2 |
Gómez, Alejandra Segura, Rodrigo Doctorovich, Fabio Pellegrino, Juan Gaviglio, Carina del Valle Guerrero, Paulina Klahn, A. Hugo Fuentealba, Mauricio Garland, María Teresa |
| author2_role |
author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Rhenium Nitrosyl Cyclopentadienyl Functionalized https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| topic |
Rhenium Nitrosyl Cyclopentadienyl Functionalized https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| description |
The UV irradiation of a hexane solution of the complex (h5 -C5Me4(CH2)2NMe2)Re(CO)3 (1) afforded the chelated species (h5 :h1 -C5Me4(CH2)2NMe2)Re(CO)2 (2). The molecular structure of 2 has been determined by X-ray crystallography. The reaction of 2 with two-electron donor ligands yields (h5 - C5Me4(CH2)2NMe2)Re(CO)2(L) (1, L ¼ CO; 3, L ¼ PMe3). The chelated species 2 also reacts with MeOTf, HBF4, and I2 to form the cationic compounds trans-[(h5 -C5Me4(CH2)2NMe2)Re(CO)2X]þ ([4]D, X ¼ Me; [5]D, X ¼ H; [6]D, X ¼ I). The trans stereochemistry of 4e6 have been assigned on the basis of n(CO) IR intensities and 13C NMR spectroscopy. Also, complex 2 reacts with nitrosyl tetrafluoroborate to yield [(h5 - C5Me4(CH2)2NMe2NO)Re(CO)2(NO)]BF4 ([7]2D). The redox behavior of the {ReNO}6 complex [7]2D was studied and the products obtained after two-electron reduction were characterized by IR. DFT calculations were done to optimize the structure of [7]2D and to study the effect of the sidearm coordination on the electronic structure of a cyclopentadienyl {ReNO}8 complex. |
| publishDate |
2014 |
| dc.date.none.fl_str_mv |
2014-05 |
| 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/11336/31816 Garland, María Teresa; Fuentealba, Mauricio; Klahn, A. Hugo; Guerrero, Paulina; Gaviglio, Carina del Valle; Pellegrino, Juan; et al.; Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative; Elsevier Science Sa; Journal of Organometallic Chemistry; 765; 5-2014; 8-16 0022-328X CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/31816 |
| identifier_str_mv |
Garland, María Teresa; Fuentealba, Mauricio; Klahn, A. Hugo; Guerrero, Paulina; Gaviglio, Carina del Valle; Pellegrino, Juan; et al.; Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative; Elsevier Science Sa; Journal of Organometallic Chemistry; 765; 5-2014; 8-16 0022-328X CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jorganchem.2014.04.019 info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0022328X14001892 |
| 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/ |
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application/pdf application/pdf application/pdf application/pdf |
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Elsevier Science Sa |
| publisher.none.fl_str_mv |
Elsevier Science Sa |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
| 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_ |
1799195829245837312 |
| spelling |
Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivativeGodoy, FernandoGómez, AlejandraSegura, RodrigoDoctorovich, FabioPellegrino, JuanGaviglio, Carina del ValleGuerrero, PaulinaKlahn, A. HugoFuentealba, MauricioGarland, María TeresaRheniumNitrosylCyclopentadienyl Functionalizedhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The UV irradiation of a hexane solution of the complex (h5 -C5Me4(CH2)2NMe2)Re(CO)3 (1) afforded the chelated species (h5 :h1 -C5Me4(CH2)2NMe2)Re(CO)2 (2). The molecular structure of 2 has been determined by X-ray crystallography. The reaction of 2 with two-electron donor ligands yields (h5 - C5Me4(CH2)2NMe2)Re(CO)2(L) (1, L ¼ CO; 3, L ¼ PMe3). The chelated species 2 also reacts with MeOTf, HBF4, and I2 to form the cationic compounds trans-[(h5 -C5Me4(CH2)2NMe2)Re(CO)2X]þ ([4]D, X ¼ Me; [5]D, X ¼ H; [6]D, X ¼ I). The trans stereochemistry of 4e6 have been assigned on the basis of n(CO) IR intensities and 13C NMR spectroscopy. Also, complex 2 reacts with nitrosyl tetrafluoroborate to yield [(h5 - C5Me4(CH2)2NMe2NO)Re(CO)2(NO)]BF4 ([7]2D). The redox behavior of the {ReNO}6 complex [7]2D was studied and the products obtained after two-electron reduction were characterized by IR. DFT calculations were done to optimize the structure of [7]2D and to study the effect of the sidearm coordination on the electronic structure of a cyclopentadienyl {ReNO}8 complex.Fil: Godoy, Fernando. Universidad de Santiago de Chile; ChileFil: Gómez, Alejandra. Universidad de Santiago de Chile; ChileFil: Segura, Rodrigo. Universidad de Santiago de Chile; ChileFil: Doctorovich, Fabio. 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: Pellegrino, Juan. 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: Gaviglio, Carina del Valle. 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: Guerrero, Paulina. Pontificia Universidad Católica de Valparaíso; ChileFil: Klahn, A. Hugo. Pontificia Universidad Católica de Valparaíso; ChileFil: Fuentealba, Mauricio. Pontificia Universidad Católica de Valparaíso; ChileFil: Garland, María Teresa. Universidad de Chile; ChileElsevier Science Sa2014-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/31816Garland, María Teresa; Fuentealba, Mauricio; Klahn, A. Hugo; Guerrero, Paulina; Gaviglio, Carina del Valle; Pellegrino, Juan; et al.; Synthesis, structure, and reactivity of (η5:η1-C5Me4(CH2)2NMe2)Re(CO)2. Electron transfer behavior of a nitrosyl derivative; Elsevier Science Sa; Journal of Organometallic Chemistry; 765; 5-2014; 8-160022-328XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.jorganchem.2014.04.019info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0022328X14001892info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2024-05-08T14:05:13Zoai:ri.conicet.gov.ar:11336/31816instacron: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:34982024-05-08 14:05:13.655CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
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15,811543 |