Single-crystal X-ray diffraction dataset for 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine

The data in this article are related to the research article “Utilizing the Regioselectivity of Perfluoropyridine towards the Preparation of Phenyoxyacetylene Precursors for Partially Fluorinated Polymers of Diverse Architecture.”(1) The X-ray structure analysis of 3,5-difluoro-2,6-bis(4-iodophenoxy...

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Autores principales: Peloquin, Andrew J., Kobra, Khadijutal, Corley, Cynthia A., McMillen, Colin D., Knoerzer, Timm A., Pennington, William T., Iacono, Scott T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938893/
https://www.ncbi.nlm.nih.gov/pubmed/31909100
http://dx.doi.org/10.1016/j.dib.2019.104956
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author Peloquin, Andrew J.
Kobra, Khadijutal
Corley, Cynthia A.
McMillen, Colin D.
Knoerzer, Timm A.
Pennington, William T.
Iacono, Scott T.
author_facet Peloquin, Andrew J.
Kobra, Khadijutal
Corley, Cynthia A.
McMillen, Colin D.
Knoerzer, Timm A.
Pennington, William T.
Iacono, Scott T.
author_sort Peloquin, Andrew J.
collection PubMed
description The data in this article are related to the research article “Utilizing the Regioselectivity of Perfluoropyridine towards the Preparation of Phenyoxyacetylene Precursors for Partially Fluorinated Polymers of Diverse Architecture.”(1) The X-ray structure analysis of 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine has revealed an asymmetric unit containing two molecules, linked via both Type I and Type II C–I∙∙∙I–C halogen bonding interactions. The packing is further consolidated via Ar–H∙∙∙π interactions. This compound has been utilized for the synthesis of monomers for linear and network polymers.
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spelling pubmed-69388932020-01-06 Single-crystal X-ray diffraction dataset for 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine Peloquin, Andrew J. Kobra, Khadijutal Corley, Cynthia A. McMillen, Colin D. Knoerzer, Timm A. Pennington, William T. Iacono, Scott T. Data Brief Chemistry The data in this article are related to the research article “Utilizing the Regioselectivity of Perfluoropyridine towards the Preparation of Phenyoxyacetylene Precursors for Partially Fluorinated Polymers of Diverse Architecture.”(1) The X-ray structure analysis of 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine has revealed an asymmetric unit containing two molecules, linked via both Type I and Type II C–I∙∙∙I–C halogen bonding interactions. The packing is further consolidated via Ar–H∙∙∙π interactions. This compound has been utilized for the synthesis of monomers for linear and network polymers. Elsevier 2019-12-13 /pmc/articles/PMC6938893/ /pubmed/31909100 http://dx.doi.org/10.1016/j.dib.2019.104956 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Chemistry
Peloquin, Andrew J.
Kobra, Khadijutal
Corley, Cynthia A.
McMillen, Colin D.
Knoerzer, Timm A.
Pennington, William T.
Iacono, Scott T.
Single-crystal X-ray diffraction dataset for 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine
title Single-crystal X-ray diffraction dataset for 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine
title_full Single-crystal X-ray diffraction dataset for 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine
title_fullStr Single-crystal X-ray diffraction dataset for 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine
title_full_unstemmed Single-crystal X-ray diffraction dataset for 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine
title_short Single-crystal X-ray diffraction dataset for 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine
title_sort single-crystal x-ray diffraction dataset for 3,5-difluoro-2,6-bis(4-iodophenoxy)-4-phenoxypyridine
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938893/
https://www.ncbi.nlm.nih.gov/pubmed/31909100
http://dx.doi.org/10.1016/j.dib.2019.104956
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