(4-Cyano­phenolato)(subphthalocyaninato)boron

The crystal structure of the title compound, C(31)H(16)BN(7)O, (CNPhO-BsubPc) is characterized by pairs of π–π stacking inter­actions between the concave faces of inversion-related BsubPc fragments with a centroid–centroid distance of 3.600 (1) Å. In addition, these pairs of mol­ecules are linked in...

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Detalles Bibliográficos
Autores principales: Paton, Andrew S., Lough, Alan J., Bender, Timothy P.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051429/
https://www.ncbi.nlm.nih.gov/pubmed/21523157
http://dx.doi.org/10.1107/S1600536811000869
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author Paton, Andrew S.
Lough, Alan J.
Bender, Timothy P.
author_facet Paton, Andrew S.
Lough, Alan J.
Bender, Timothy P.
author_sort Paton, Andrew S.
collection PubMed
description The crystal structure of the title compound, C(31)H(16)BN(7)O, (CNPhO-BsubPc) is characterized by pairs of π–π stacking inter­actions between the concave faces of inversion-related BsubPc fragments with a centroid–centroid distance of 3.600 (1) Å. In addition, these pairs of mol­ecules are linked into chains along [101] through further weak π–π stacking inter­actions with a centroid–centroid distance of 3.8587 (9) Å. There are also weak C—H⋯π(arene) inter­actions within the chains.
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spelling pubmed-30514292011-04-26 (4-Cyano­phenolato)(subphthalocyaninato)boron Paton, Andrew S. Lough, Alan J. Bender, Timothy P. Acta Crystallogr Sect E Struct Rep Online Organic Papers The crystal structure of the title compound, C(31)H(16)BN(7)O, (CNPhO-BsubPc) is characterized by pairs of π–π stacking inter­actions between the concave faces of inversion-related BsubPc fragments with a centroid–centroid distance of 3.600 (1) Å. In addition, these pairs of mol­ecules are linked into chains along [101] through further weak π–π stacking inter­actions with a centroid–centroid distance of 3.8587 (9) Å. There are also weak C—H⋯π(arene) inter­actions within the chains. International Union of Crystallography 2011-01-29 /pmc/articles/PMC3051429/ /pubmed/21523157 http://dx.doi.org/10.1107/S1600536811000869 Text en © Paton et al. 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
Paton, Andrew S.
Lough, Alan J.
Bender, Timothy P.
(4-Cyano­phenolato)(subphthalocyaninato)boron
title (4-Cyano­phenolato)(subphthalocyaninato)boron
title_full (4-Cyano­phenolato)(subphthalocyaninato)boron
title_fullStr (4-Cyano­phenolato)(subphthalocyaninato)boron
title_full_unstemmed (4-Cyano­phenolato)(subphthalocyaninato)boron
title_short (4-Cyano­phenolato)(subphthalocyaninato)boron
title_sort (4-cyano­phenolato)(subphthalocyaninato)boron
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051429/
https://www.ncbi.nlm.nih.gov/pubmed/21523157
http://dx.doi.org/10.1107/S1600536811000869
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AT loughalanj 4cyanophenolatosubphthalocyaninatoboron
AT bendertimothyp 4cyanophenolatosubphthalocyaninatoboron

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