Cargando…

2,6-Bis(4-methoxy­phen­yl)-4-phenyl­pyridine

In the title compound, C(25)H(21)NO(2), which was synthesized by the condensation of 2,6-bis­(4-methoxy­phen­yl)-4-phenyl­pyridinium tetra­fluoro­borate with ammonia under microwave irradiation and solvent-free conditions, the angles between the central pyridine ring and the three benzene rings are...

Descripción completa

Detalles Bibliográficos
Autor principal: Dong, Xiaoning
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980106/
https://www.ncbi.nlm.nih.gov/pubmed/21580143
http://dx.doi.org/10.1107/S1600536809051277
_version_ 1782191578809368576
author Dong, Xiaoning
author_facet Dong, Xiaoning
author_sort Dong, Xiaoning
collection PubMed
description In the title compound, C(25)H(21)NO(2), which was synthesized by the condensation of 2,6-bis­(4-methoxy­phen­yl)-4-phenyl­pyridinium tetra­fluoro­borate with ammonia under microwave irradiation and solvent-free conditions, the angles between the central pyridine ring and the three benzene rings are 22.3 (2), 35.3 (2) and 19.8 (2)°. In the crystal, inter­molecular C—H⋯π hydrogen-bond inter­actions link the mol­ecules.
format Text
id pubmed-2980106
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29801062010-12-30 2,6-Bis(4-methoxy­phen­yl)-4-phenyl­pyridine Dong, Xiaoning Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(25)H(21)NO(2), which was synthesized by the condensation of 2,6-bis­(4-methoxy­phen­yl)-4-phenyl­pyridinium tetra­fluoro­borate with ammonia under microwave irradiation and solvent-free conditions, the angles between the central pyridine ring and the three benzene rings are 22.3 (2), 35.3 (2) and 19.8 (2)°. In the crystal, inter­molecular C—H⋯π hydrogen-bond inter­actions link the mol­ecules. International Union of Crystallography 2009-12-04 /pmc/articles/PMC2980106/ /pubmed/21580143 http://dx.doi.org/10.1107/S1600536809051277 Text en © Xiaoning Dong 2010 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
Dong, Xiaoning
2,6-Bis(4-methoxy­phen­yl)-4-phenyl­pyridine
title 2,6-Bis(4-methoxy­phen­yl)-4-phenyl­pyridine
title_full 2,6-Bis(4-methoxy­phen­yl)-4-phenyl­pyridine
title_fullStr 2,6-Bis(4-methoxy­phen­yl)-4-phenyl­pyridine
title_full_unstemmed 2,6-Bis(4-methoxy­phen­yl)-4-phenyl­pyridine
title_short 2,6-Bis(4-methoxy­phen­yl)-4-phenyl­pyridine
title_sort 2,6-bis(4-methoxy­phen­yl)-4-phenyl­pyridine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980106/
https://www.ncbi.nlm.nih.gov/pubmed/21580143
http://dx.doi.org/10.1107/S1600536809051277
work_keys_str_mv AT dongxiaoning 26bis4methoxyphenyl4phenylpyridine