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Phenyl Derivative of Iron 5,10,15-Tritolylcorrole
[Image: see text] The phenyl–iron complex of 5,10,15-tritolylcorrole was prepared by reaction of the starting chloro–iron complex with phenylmagnesium bromide in dichloromethane. The organometallic complex was fully characterized by a combination of spectroscopic methods, X-ray crystallography, and...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4002138/ https://www.ncbi.nlm.nih.gov/pubmed/24697623 http://dx.doi.org/10.1021/ic5003572 |
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author | Nardis, Sara Cicero, Daniel O. Licoccia, Silvia Pomarico, Giuseppe Berionni Berna, Beatrice Sette, Marco Ricciardi, Giampaolo Rosa, Angela Fronczek, Frank R. Smith, Kevin M. Paolesse, Roberto |
author_facet | Nardis, Sara Cicero, Daniel O. Licoccia, Silvia Pomarico, Giuseppe Berionni Berna, Beatrice Sette, Marco Ricciardi, Giampaolo Rosa, Angela Fronczek, Frank R. Smith, Kevin M. Paolesse, Roberto |
author_sort | Nardis, Sara |
collection | PubMed |
description | [Image: see text] The phenyl–iron complex of 5,10,15-tritolylcorrole was prepared by reaction of the starting chloro–iron complex with phenylmagnesium bromide in dichloromethane. The organometallic complex was fully characterized by a combination of spectroscopic methods, X-ray crystallography, and density functional theory (DFT) calculations. All of these techniques support the description of the electronic structure of this phenyl–iron derivative as a low-spin iron(IV) coordinated to a closed-shell corrolate trianion and to a phenyl monoanion. Complete assignments of the (1)H and (13)C NMR spectra of the phenyl–iron derivative and the starting chloro–iron complex were performed on the basis of the NMR spectra of the regioselectively β-substituted bromo derivatives and the DFT calculations. |
format | Online Article Text |
id | pubmed-4002138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-40021382015-04-03 Phenyl Derivative of Iron 5,10,15-Tritolylcorrole Nardis, Sara Cicero, Daniel O. Licoccia, Silvia Pomarico, Giuseppe Berionni Berna, Beatrice Sette, Marco Ricciardi, Giampaolo Rosa, Angela Fronczek, Frank R. Smith, Kevin M. Paolesse, Roberto Inorg Chem [Image: see text] The phenyl–iron complex of 5,10,15-tritolylcorrole was prepared by reaction of the starting chloro–iron complex with phenylmagnesium bromide in dichloromethane. The organometallic complex was fully characterized by a combination of spectroscopic methods, X-ray crystallography, and density functional theory (DFT) calculations. All of these techniques support the description of the electronic structure of this phenyl–iron derivative as a low-spin iron(IV) coordinated to a closed-shell corrolate trianion and to a phenyl monoanion. Complete assignments of the (1)H and (13)C NMR spectra of the phenyl–iron derivative and the starting chloro–iron complex were performed on the basis of the NMR spectra of the regioselectively β-substituted bromo derivatives and the DFT calculations. American Chemical Society 2014-04-03 2014-04-21 /pmc/articles/PMC4002138/ /pubmed/24697623 http://dx.doi.org/10.1021/ic5003572 Text en Copyright © 2014 American Chemical Society |
spellingShingle | Nardis, Sara Cicero, Daniel O. Licoccia, Silvia Pomarico, Giuseppe Berionni Berna, Beatrice Sette, Marco Ricciardi, Giampaolo Rosa, Angela Fronczek, Frank R. Smith, Kevin M. Paolesse, Roberto Phenyl Derivative of Iron 5,10,15-Tritolylcorrole |
title | Phenyl Derivative of Iron 5,10,15-Tritolylcorrole |
title_full | Phenyl Derivative of Iron 5,10,15-Tritolylcorrole |
title_fullStr | Phenyl Derivative of Iron 5,10,15-Tritolylcorrole |
title_full_unstemmed | Phenyl Derivative of Iron 5,10,15-Tritolylcorrole |
title_short | Phenyl Derivative of Iron 5,10,15-Tritolylcorrole |
title_sort | phenyl derivative of iron 5,10,15-tritolylcorrole |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4002138/ https://www.ncbi.nlm.nih.gov/pubmed/24697623 http://dx.doi.org/10.1021/ic5003572 |
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