1,6-Bis[(2,2′:6′,2′′-terpyridin-4′-yl)­oxy]hexa­ne

The mol­ecule of the title compound, C(36)H(32)N(6)O(2), lies about an inversion center, located at the mid-point of the central C—C bond of the diether bridge. The terminal pyridine rings form dihedral angles of 4.67 (7) and 26.23 (7)° with the central ring. In the crystal, weak C—H⋯N and C—H⋯O int...

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Detalles Bibliográficos
Autores principales: Nikolayenko, Varvara I., Akerman, Matthew P., Grimmer, Craig D., Reddy, Desigan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394054/
https://www.ncbi.nlm.nih.gov/pubmed/22798919
http://dx.doi.org/10.1107/S1600536812029017
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author Nikolayenko, Varvara I.
Akerman, Matthew P.
Grimmer, Craig D.
Reddy, Desigan
author_facet Nikolayenko, Varvara I.
Akerman, Matthew P.
Grimmer, Craig D.
Reddy, Desigan
author_sort Nikolayenko, Varvara I.
collection PubMed
description The mol­ecule of the title compound, C(36)H(32)N(6)O(2), lies about an inversion center, located at the mid-point of the central C—C bond of the diether bridge. The terminal pyridine rings form dihedral angles of 4.67 (7) and 26.23 (7)° with the central ring. In the crystal, weak C—H⋯N and C—H⋯O inter­actions link the mol­ecules into a three-dimensional network.
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spelling pubmed-33940542012-07-13 1,6-Bis[(2,2′:6′,2′′-terpyridin-4′-yl)­oxy]hexa­ne Nikolayenko, Varvara I. Akerman, Matthew P. Grimmer, Craig D. Reddy, Desigan Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title compound, C(36)H(32)N(6)O(2), lies about an inversion center, located at the mid-point of the central C—C bond of the diether bridge. The terminal pyridine rings form dihedral angles of 4.67 (7) and 26.23 (7)° with the central ring. In the crystal, weak C—H⋯N and C—H⋯O inter­actions link the mol­ecules into a three-dimensional network. International Union of Crystallography 2012-06-30 /pmc/articles/PMC3394054/ /pubmed/22798919 http://dx.doi.org/10.1107/S1600536812029017 Text en © Nikolayenko et al. 2012 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
Nikolayenko, Varvara I.
Akerman, Matthew P.
Grimmer, Craig D.
Reddy, Desigan
1,6-Bis[(2,2′:6′,2′′-terpyridin-4′-yl)­oxy]hexa­ne
title 1,6-Bis[(2,2′:6′,2′′-terpyridin-4′-yl)­oxy]hexa­ne
title_full 1,6-Bis[(2,2′:6′,2′′-terpyridin-4′-yl)­oxy]hexa­ne
title_fullStr 1,6-Bis[(2,2′:6′,2′′-terpyridin-4′-yl)­oxy]hexa­ne
title_full_unstemmed 1,6-Bis[(2,2′:6′,2′′-terpyridin-4′-yl)­oxy]hexa­ne
title_short 1,6-Bis[(2,2′:6′,2′′-terpyridin-4′-yl)­oxy]hexa­ne
title_sort 1,6-bis[(2,2′:6′,2′′-terpyridin-4′-yl)­oxy]hexa­ne
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394054/
https://www.ncbi.nlm.nih.gov/pubmed/22798919
http://dx.doi.org/10.1107/S1600536812029017
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AT reddydesigan 16bis2262terpyridin4yloxyhexane

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