2,5-Bis[(E)-2-phenyl­ethen­yl]-3,6-bis­(pyridin-2-yl)pyrazine

The mol­ecule of the title compound, C(30)H(22)N(4), exhibits inversion symmetry adopting the shape of a St Andrew’s Cross. It shows dihedral angles between adjacent aryl units of around 50° whereas torsion angles of ca 10° are found along the aryl­ene vinyl­ene path. [Image: see text]

Detalles Bibliográficos
Autores principales: Detert, Heiner, Jochem, Matthias, Schollmeyer, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462200/
https://www.ncbi.nlm.nih.gov/pubmed/36339482
http://dx.doi.org/10.1107/S2414314620003727
_version_ 1784787129528745984
author Detert, Heiner
Jochem, Matthias
Schollmeyer, Dieter
author_facet Detert, Heiner
Jochem, Matthias
Schollmeyer, Dieter
author_sort Detert, Heiner
collection PubMed
description The mol­ecule of the title compound, C(30)H(22)N(4), exhibits inversion symmetry adopting the shape of a St Andrew’s Cross. It shows dihedral angles between adjacent aryl units of around 50° whereas torsion angles of ca 10° are found along the aryl­ene vinyl­ene path. [Image: see text]
format Online
Article
Text
id pubmed-9462200
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-94622002022-11-04 2,5-Bis[(E)-2-phenyl­ethen­yl]-3,6-bis­(pyridin-2-yl)pyrazine Detert, Heiner Jochem, Matthias Schollmeyer, Dieter IUCrdata Data Reports The mol­ecule of the title compound, C(30)H(22)N(4), exhibits inversion symmetry adopting the shape of a St Andrew’s Cross. It shows dihedral angles between adjacent aryl units of around 50° whereas torsion angles of ca 10° are found along the aryl­ene vinyl­ene path. [Image: see text] International Union of Crystallography 2020-03-17 /pmc/articles/PMC9462200/ /pubmed/36339482 http://dx.doi.org/10.1107/S2414314620003727 Text en © Detert et al. 2020 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Detert, Heiner
Jochem, Matthias
Schollmeyer, Dieter
2,5-Bis[(E)-2-phenyl­ethen­yl]-3,6-bis­(pyridin-2-yl)pyrazine
title 2,5-Bis[(E)-2-phenyl­ethen­yl]-3,6-bis­(pyridin-2-yl)pyrazine
title_full 2,5-Bis[(E)-2-phenyl­ethen­yl]-3,6-bis­(pyridin-2-yl)pyrazine
title_fullStr 2,5-Bis[(E)-2-phenyl­ethen­yl]-3,6-bis­(pyridin-2-yl)pyrazine
title_full_unstemmed 2,5-Bis[(E)-2-phenyl­ethen­yl]-3,6-bis­(pyridin-2-yl)pyrazine
title_short 2,5-Bis[(E)-2-phenyl­ethen­yl]-3,6-bis­(pyridin-2-yl)pyrazine
title_sort 2,5-bis[(e)-2-phenyl­ethen­yl]-3,6-bis­(pyridin-2-yl)pyrazine
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462200/
https://www.ncbi.nlm.nih.gov/pubmed/36339482
http://dx.doi.org/10.1107/S2414314620003727
work_keys_str_mv AT detertheiner 25bise2phenylethenyl36bispyridin2ylpyrazine
AT jochemmatthias 25bise2phenylethenyl36bispyridin2ylpyrazine
AT schollmeyerdieter 25bise2phenylethenyl36bispyridin2ylpyrazine

Ejemplares similares