Difluoro­[2-(quinolin-2-yl)phenolato]borane

The title compound, C(15)H(10)BF(2)NO, was synthesized by the reaction of 2-(quinolin-2-yl)phenol and boron trifluoride etherate. The quinoline ring system and the benzene ring are twisted, making a dihedral angle of 8.3 (2)°. In the crystal, π–π inter­actions between the aromatic rings [centroid–ce...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Xi, Xia, Min
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089244/
https://www.ncbi.nlm.nih.gov/pubmed/21754376
http://dx.doi.org/10.1107/S1600536811011895
_version_ 1782203011574005760
author Yang, Xi
Xia, Min
author_facet Yang, Xi
Xia, Min
author_sort Yang, Xi
collection PubMed
description The title compound, C(15)H(10)BF(2)NO, was synthesized by the reaction of 2-(quinolin-2-yl)phenol and boron trifluoride etherate. The quinoline ring system and the benzene ring are twisted, making a dihedral angle of 8.3 (2)°. In the crystal, π–π inter­actions between the aromatic rings [centroid–centroid distance = 3.638 (9) Å] link the mol­ecules into chains propagating in [100].
format Text
id pubmed-3089244
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-30892442011-07-13 Difluoro­[2-(quinolin-2-yl)phenolato]borane Yang, Xi Xia, Min Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(10)BF(2)NO, was synthesized by the reaction of 2-(quinolin-2-yl)phenol and boron trifluoride etherate. The quinoline ring system and the benzene ring are twisted, making a dihedral angle of 8.3 (2)°. In the crystal, π–π inter­actions between the aromatic rings [centroid–centroid distance = 3.638 (9) Å] link the mol­ecules into chains propagating in [100]. International Union of Crystallography 2011-04-07 /pmc/articles/PMC3089244/ /pubmed/21754376 http://dx.doi.org/10.1107/S1600536811011895 Text en © Yang and Xia 2011 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
Yang, Xi
Xia, Min
Difluoro­[2-(quinolin-2-yl)phenolato]borane
title Difluoro­[2-(quinolin-2-yl)phenolato]borane
title_full Difluoro­[2-(quinolin-2-yl)phenolato]borane
title_fullStr Difluoro­[2-(quinolin-2-yl)phenolato]borane
title_full_unstemmed Difluoro­[2-(quinolin-2-yl)phenolato]borane
title_short Difluoro­[2-(quinolin-2-yl)phenolato]borane
title_sort difluoro­[2-(quinolin-2-yl)phenolato]borane
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089244/
https://www.ncbi.nlm.nih.gov/pubmed/21754376
http://dx.doi.org/10.1107/S1600536811011895
work_keys_str_mv AT yangxi difluoro2quinolin2ylphenolatoborane
AT xiamin difluoro2quinolin2ylphenolatoborane

Ejemplares similares