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1,3-Bis(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)-2,2-bis­[(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)meth­yl]propane

In the crystal structure of the title compound, C(29)H(8)F(16)I(4)O(4), short I⋯I and I⋯F contacts, which can be understood as halogen bonds (XBs), represent the strongest inter­molecular inter­actions, consistent with the presence of I and F atoms, and the absence of H atoms, at the periphery of th...

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Detalles Bibliográficos
Autores principales: Cavallo, Gabriella, Metrangolo, Pierangelo, Pilati, Tullio, Resnati, Giuseppe, Terraneo, Giancarlo, Ursini, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629626/
https://www.ncbi.nlm.nih.gov/pubmed/23634113
http://dx.doi.org/10.1107/S1600536813007605
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author Cavallo, Gabriella
Metrangolo, Pierangelo
Pilati, Tullio
Resnati, Giuseppe
Terraneo, Giancarlo
Ursini, Maurizio
author_facet Cavallo, Gabriella
Metrangolo, Pierangelo
Pilati, Tullio
Resnati, Giuseppe
Terraneo, Giancarlo
Ursini, Maurizio
author_sort Cavallo, Gabriella
collection PubMed
description In the crystal structure of the title compound, C(29)H(8)F(16)I(4)O(4), short I⋯I and I⋯F contacts, which can be understood as halogen bonds (XBs), represent the strongest inter­molecular inter­actions, consistent with the presence of I and F atoms, and the absence of H atoms, at the periphery of the mol­ecule. In addition, π–π stacking inter­actions between tetra­fluoro­iodo­phenyl (TFIP) groups and five short F⋯F inter­actions are present.
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spelling pubmed-36296262013-04-30 1,3-Bis(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)-2,2-bis­[(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)meth­yl]propane Cavallo, Gabriella Metrangolo, Pierangelo Pilati, Tullio Resnati, Giuseppe Terraneo, Giancarlo Ursini, Maurizio Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(29)H(8)F(16)I(4)O(4), short I⋯I and I⋯F contacts, which can be understood as halogen bonds (XBs), represent the strongest inter­molecular inter­actions, consistent with the presence of I and F atoms, and the absence of H atoms, at the periphery of the mol­ecule. In addition, π–π stacking inter­actions between tetra­fluoro­iodo­phenyl (TFIP) groups and five short F⋯F inter­actions are present. International Union of Crystallography 2013-03-23 /pmc/articles/PMC3629626/ /pubmed/23634113 http://dx.doi.org/10.1107/S1600536813007605 Text en © Cavallo et al. 2013 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Cavallo, Gabriella
Metrangolo, Pierangelo
Pilati, Tullio
Resnati, Giuseppe
Terraneo, Giancarlo
Ursini, Maurizio
1,3-Bis(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)-2,2-bis­[(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)meth­yl]propane
title 1,3-Bis(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)-2,2-bis­[(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)meth­yl]propane
title_full 1,3-Bis(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)-2,2-bis­[(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)meth­yl]propane
title_fullStr 1,3-Bis(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)-2,2-bis­[(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)meth­yl]propane
title_full_unstemmed 1,3-Bis(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)-2,2-bis­[(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)meth­yl]propane
title_short 1,3-Bis(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)-2,2-bis­[(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)meth­yl]propane
title_sort 1,3-bis(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)-2,2-bis­[(2,3,5,6-tetra­fluoro-4-iodo­phen­oxy)meth­yl]propane
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629626/
https://www.ncbi.nlm.nih.gov/pubmed/23634113
http://dx.doi.org/10.1107/S1600536813007605
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