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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
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.
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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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