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(4-Acetyl­phenolato)(subphthalo­cyaninato)boron(III)

In the title compound, C(32)H(19)BN(6)O(2), the B atom adopts a BON(3) tetra­hedral coordination geometry. In the crystal, pairs of mol­ecules are associated through aromatic π–π stacking inter­actions between the concave faces of the boronsubphthalocyanine fragments at a centroid–centroid distance...

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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 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011621/
https://www.ncbi.nlm.nih.gov/pubmed/21589533
http://dx.doi.org/10.1107/S1600536810046003
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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 In the title compound, C(32)H(19)BN(6)O(2), the B atom adopts a BON(3) tetra­hedral coordination geometry. In the crystal, pairs of mol­ecules are associated through aromatic π–π stacking inter­actions between the concave faces of the boronsubphthalocyanine fragments at a centroid–centroid distance of 3.4951 (19) Å and a weaker inter­action of the same type between the convex faces of the same group [centroid–centroid separation = 3.5669 (18) Å] also occurs.
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spelling pubmed-30116212010-12-30 (4-Acetyl­phenolato)(subphthalo­cyaninato)boron(III) Paton, Andrew S. Lough, Alan J. Bender, Timothy P. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(32)H(19)BN(6)O(2), the B atom adopts a BON(3) tetra­hedral coordination geometry. In the crystal, pairs of mol­ecules are associated through aromatic π–π stacking inter­actions between the concave faces of the boronsubphthalocyanine fragments at a centroid–centroid distance of 3.4951 (19) Å and a weaker inter­action of the same type between the convex faces of the same group [centroid–centroid separation = 3.5669 (18) Å] also occurs. International Union of Crystallography 2010-11-20 /pmc/articles/PMC3011621/ /pubmed/21589533 http://dx.doi.org/10.1107/S1600536810046003 Text en © Paton et al. 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
Paton, Andrew S.
Lough, Alan J.
Bender, Timothy P.
(4-Acetyl­phenolato)(subphthalo­cyaninato)boron(III)
title (4-Acetyl­phenolato)(subphthalo­cyaninato)boron(III)
title_full (4-Acetyl­phenolato)(subphthalo­cyaninato)boron(III)
title_fullStr (4-Acetyl­phenolato)(subphthalo­cyaninato)boron(III)
title_full_unstemmed (4-Acetyl­phenolato)(subphthalo­cyaninato)boron(III)
title_short (4-Acetyl­phenolato)(subphthalo­cyaninato)boron(III)
title_sort (4-acetyl­phenolato)(subphthalo­cyaninato)boron(iii)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011621/
https://www.ncbi.nlm.nih.gov/pubmed/21589533
http://dx.doi.org/10.1107/S1600536810046003
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