1,4-Bis(iodo­meth­yl)benzene

The centrosymmetric title compound, C(8)H(8)I(2), was prepared by metathesis from the dibromo analogue. In the crystal structure, weak C—H⋯I inter­actions link the mol­ecules into stacks down the b axis. The structure is further stabilized by short I⋯I contacts [3.8433 (2) Å], forming undulating she...

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Detalles Bibliográficos
Autores principales: McAdam, C. John, Hanton, Lyall R., Moratti, Stephen C., Simpson, Jim
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969495/
https://www.ncbi.nlm.nih.gov/pubmed/21582852
http://dx.doi.org/10.1107/S1600536809021151
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author McAdam, C. John
Hanton, Lyall R.
Moratti, Stephen C.
Simpson, Jim
author_facet McAdam, C. John
Hanton, Lyall R.
Moratti, Stephen C.
Simpson, Jim
author_sort McAdam, C. John
collection PubMed
description The centrosymmetric title compound, C(8)H(8)I(2), was prepared by metathesis from the dibromo analogue. In the crystal structure, weak C—H⋯I inter­actions link the mol­ecules into stacks down the b axis. The structure is further stabilized by short I⋯I contacts [3.8433 (2) Å], forming undulating sheets in the (101) plane.
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spelling pubmed-29694952010-12-30 1,4-Bis(iodo­meth­yl)benzene McAdam, C. John Hanton, Lyall R. Moratti, Stephen C. Simpson, Jim Acta Crystallogr Sect E Struct Rep Online Organic Papers The centrosymmetric title compound, C(8)H(8)I(2), was prepared by metathesis from the dibromo analogue. In the crystal structure, weak C—H⋯I inter­actions link the mol­ecules into stacks down the b axis. The structure is further stabilized by short I⋯I contacts [3.8433 (2) Å], forming undulating sheets in the (101) plane. International Union of Crystallography 2009-06-13 /pmc/articles/PMC2969495/ /pubmed/21582852 http://dx.doi.org/10.1107/S1600536809021151 Text en © McAdam et al. 2009 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
McAdam, C. John
Hanton, Lyall R.
Moratti, Stephen C.
Simpson, Jim
1,4-Bis(iodo­meth­yl)benzene
title 1,4-Bis(iodo­meth­yl)benzene
title_full 1,4-Bis(iodo­meth­yl)benzene
title_fullStr 1,4-Bis(iodo­meth­yl)benzene
title_full_unstemmed 1,4-Bis(iodo­meth­yl)benzene
title_short 1,4-Bis(iodo­meth­yl)benzene
title_sort 1,4-bis(iodo­meth­yl)benzene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969495/
https://www.ncbi.nlm.nih.gov/pubmed/21582852
http://dx.doi.org/10.1107/S1600536809021151
work_keys_str_mv AT mcadamcjohn 14bisiodomethylbenzene
AT hantonlyallr 14bisiodomethylbenzene
AT morattistephenc 14bisiodomethylbenzene
AT simpsonjim 14bisiodomethylbenzene

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