Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterization
- Autores
- Maisuls, Iván; Wolcan, Ezequiel; Piro, Oscar Enrique; Echeverría, Gustavo Alberto; Petroselli, Gabriela; Erra Balsells, Rosa; Cabrerizo, Franco Martín; Ruiz, Gustavo Teodosio
- Año de publicación
- 2015
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Two novel Re(I) complexes with the general formula fac-[Re(CO)3(L)(nHo)]CF33SO3, where L = 2,2’-bipyridine (bpy) or 1,10 phenanthroline (phen) and nHo (9H-pyrido[3,4-b]indole; norharmane) have been synthesized. The Re(I)–nHo complexes were characterized by structural X-ray diffraction, 1H and 13C NMR, UV-vis absorption and FT-IR spectroscopy, and by a combination of two mass spectrometry techniques, namely ESI-MS and UV-MALDI-MS. All characterizations showed that nHo is coordinated to the metal atom by the pyridine nitrogen of the molecule. X-ray structural analysis revealed that the crystal lattices for both complexes are further stabilized by a strong >N–H⋯O bond between the pyrrole NH group of the pyridoindole ligand and one oxygen atom of the trifluoromethanesulfonate counter-ion. Ground state geometry optimization by DFT calculations showed that in fluid solution the nHo ligand may rotate freely. The nature of the electronic transitions of Re(CO)3(bpy)(nHo)⁺ were established by TD-DFT calculations. The set of the most important electronic transitions present in this complex are comprised of π → π* electronic transitions centered on bpy and nHo moieties, LLCTnHo→COs, MLLCTRe(CO)3→bpy and LLCTnHo→bpy transitions. Additionally, TD-DFT calculations predict the existence of another two intense MLLCTRe(CO)3→nHo electronic transitions. Calculated UV-vis absorption spectra are in good agreement with the corresponding experimental data for the bpy-containing complex.
Facultad de Ciencias Exactas
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
Instituto de Física La Plata - Materia
-
Ciencias Exactas
Química
Física
X-ray crystal structure
Quantum mechanical calculations
Re(I) polypyridyl complexes - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
.jpg)
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/102509
Ver los metadatos del registro completo
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Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterizationMaisuls, IvánWolcan, EzequielPiro, Oscar EnriqueEcheverría, Gustavo AlbertoPetroselli, GabrielaErra Balsells, RosaCabrerizo, Franco MartínRuiz, Gustavo TeodosioCiencias ExactasQuímicaFísicaX-ray crystal structureQuantum mechanical calculationsRe(I) polypyridyl complexesTwo novel Re(I) complexes with the general formula <i>fac</i>-[Re(CO)<sub>3</sub>(L)(nHo)]CF3<sub>3</sub>SO<sub>3</sub>, where L = 2,2’-bipyridine (bpy) or 1,10 phenanthroline (phen) and nHo (9H-pyrido[3,4-b]indole; norharmane) have been synthesized. The Re(I)–nHo complexes were characterized by structural X-ray diffraction, <sup>1</sup>H and <sup>13</sup>C NMR, UV-vis absorption and FT-IR spectroscopy, and by a combination of two mass spectrometry techniques, namely ESI-MS and UV-MALDI-MS. All characterizations showed that nHo is coordinated to the metal atom by the pyridine nitrogen of the molecule. X-ray structural analysis revealed that the crystal lattices for both complexes are further stabilized by a strong >N–H⋯O bond between the pyrrole NH group of the pyridoindole ligand and one oxygen atom of the trifluoromethanesulfonate counter-ion. Ground state geometry optimization by DFT calculations showed that in fluid solution the nHo ligand may rotate freely. The nature of the electronic transitions of Re(CO)<sub>3</sub>(bpy)(nHo)⁺ were established by TD-DFT calculations. The set of the most important electronic transitions present in this complex are comprised of π → π* electronic transitions centered on bpy and nHo moieties, LLCT<sub>nHo→COs</sub>, MLLCT<sub>Re(CO)<sub>3</sub>→bpy</sub> and LLCT<sub>nHo→bpy</sub> transitions. Additionally, TD-DFT calculations predict the existence of another two intense MLLCT<sub>Re(CO)<sub>3</sub>→nHo</sub> electronic transitions. Calculated UV-vis absorption spectra are in good agreement with the corresponding experimental data for the bpy-containing complex.Facultad de Ciencias ExactasInstituto de Investigaciones Fisicoquímicas Teóricas y AplicadasInstituto de Física La Plata2015-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf17064-17074http://sedici.unlp.edu.ar/handle/10915/102509enginfo:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/43063info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2015/DT/C5DT02790Jinfo:eu-repo/semantics/altIdentifier/issn/1477-9226info:eu-repo/semantics/altIdentifier/doi/10.1039/c5dt02790jinfo:eu-repo/semantics/altIdentifier/hdl/11336/43063info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-11-26T09:58:02Zoai:sedici.unlp.edu.ar:10915/102509Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-11-26 09:58:02.939SEDICI (UNLP) - Universidad Nacional de La Platafalse |
| dc.title.none.fl_str_mv |
Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterization |
| title |
Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterization |
| spellingShingle |
Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterization Maisuls, Iván Ciencias Exactas Química Física X-ray crystal structure Quantum mechanical calculations Re(I) polypyridyl complexes |
| title_short |
Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterization |
| title_full |
Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterization |
| title_fullStr |
Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterization |
| title_full_unstemmed |
Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterization |
| title_sort |
Norharmane rhenium(I) polypyridyl complexes: synthesis, structural and spectroscopic characterization |
| dc.creator.none.fl_str_mv |
Maisuls, Iván Wolcan, Ezequiel Piro, Oscar Enrique Echeverría, Gustavo Alberto Petroselli, Gabriela Erra Balsells, Rosa Cabrerizo, Franco Martín Ruiz, Gustavo Teodosio |
| author |
Maisuls, Iván |
| author_facet |
Maisuls, Iván Wolcan, Ezequiel Piro, Oscar Enrique Echeverría, Gustavo Alberto Petroselli, Gabriela Erra Balsells, Rosa Cabrerizo, Franco Martín Ruiz, Gustavo Teodosio |
| author_role |
author |
| author2 |
Wolcan, Ezequiel Piro, Oscar Enrique Echeverría, Gustavo Alberto Petroselli, Gabriela Erra Balsells, Rosa Cabrerizo, Franco Martín Ruiz, Gustavo Teodosio |
| author2_role |
author author author author author author author |
| dc.subject.none.fl_str_mv |
Ciencias Exactas Química Física X-ray crystal structure Quantum mechanical calculations Re(I) polypyridyl complexes |
| topic |
Ciencias Exactas Química Física X-ray crystal structure Quantum mechanical calculations Re(I) polypyridyl complexes |
| dc.description.none.fl_txt_mv |
Two novel Re(I) complexes with the general formula <i>fac</i>-[Re(CO)<sub>3</sub>(L)(nHo)]CF3<sub>3</sub>SO<sub>3</sub>, where L = 2,2’-bipyridine (bpy) or 1,10 phenanthroline (phen) and nHo (9H-pyrido[3,4-b]indole; norharmane) have been synthesized. The Re(I)–nHo complexes were characterized by structural X-ray diffraction, <sup>1</sup>H and <sup>13</sup>C NMR, UV-vis absorption and FT-IR spectroscopy, and by a combination of two mass spectrometry techniques, namely ESI-MS and UV-MALDI-MS. All characterizations showed that nHo is coordinated to the metal atom by the pyridine nitrogen of the molecule. X-ray structural analysis revealed that the crystal lattices for both complexes are further stabilized by a strong >N–H⋯O bond between the pyrrole NH group of the pyridoindole ligand and one oxygen atom of the trifluoromethanesulfonate counter-ion. Ground state geometry optimization by DFT calculations showed that in fluid solution the nHo ligand may rotate freely. The nature of the electronic transitions of Re(CO)<sub>3</sub>(bpy)(nHo)⁺ were established by TD-DFT calculations. The set of the most important electronic transitions present in this complex are comprised of π → π* electronic transitions centered on bpy and nHo moieties, LLCT<sub>nHo→COs</sub>, MLLCT<sub>Re(CO)<sub>3</sub>→bpy</sub> and LLCT<sub>nHo→bpy</sub> transitions. Additionally, TD-DFT calculations predict the existence of another two intense MLLCT<sub>Re(CO)<sub>3</sub>→nHo</sub> electronic transitions. Calculated UV-vis absorption spectra are in good agreement with the corresponding experimental data for the bpy-containing complex. Facultad de Ciencias Exactas Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas Instituto de Física La Plata |
| description |
Two novel Re(I) complexes with the general formula <i>fac</i>-[Re(CO)<sub>3</sub>(L)(nHo)]CF3<sub>3</sub>SO<sub>3</sub>, where L = 2,2’-bipyridine (bpy) or 1,10 phenanthroline (phen) and nHo (9H-pyrido[3,4-b]indole; norharmane) have been synthesized. The Re(I)–nHo complexes were characterized by structural X-ray diffraction, <sup>1</sup>H and <sup>13</sup>C NMR, UV-vis absorption and FT-IR spectroscopy, and by a combination of two mass spectrometry techniques, namely ESI-MS and UV-MALDI-MS. All characterizations showed that nHo is coordinated to the metal atom by the pyridine nitrogen of the molecule. X-ray structural analysis revealed that the crystal lattices for both complexes are further stabilized by a strong >N–H⋯O bond between the pyrrole NH group of the pyridoindole ligand and one oxygen atom of the trifluoromethanesulfonate counter-ion. Ground state geometry optimization by DFT calculations showed that in fluid solution the nHo ligand may rotate freely. The nature of the electronic transitions of Re(CO)<sub>3</sub>(bpy)(nHo)⁺ were established by TD-DFT calculations. The set of the most important electronic transitions present in this complex are comprised of π → π* electronic transitions centered on bpy and nHo moieties, LLCT<sub>nHo→COs</sub>, MLLCT<sub>Re(CO)<sub>3</sub>→bpy</sub> and LLCT<sub>nHo→bpy</sub> transitions. Additionally, TD-DFT calculations predict the existence of another two intense MLLCT<sub>Re(CO)<sub>3</sub>→nHo</sub> electronic transitions. Calculated UV-vis absorption spectra are in good agreement with the corresponding experimental data for the bpy-containing complex. |
| publishDate |
2015 |
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2015-08 |
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eng |
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eng |
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