2′-Acetonaphthone

In the structure of the title compound [systematic name: 1-(naphthalen-2-yl)ethanone], C(12)H(10)O, the acetyl group is approximately coplanar with the naphthalene ring with a C(ar)—C(ar)—C=O torsion angle of 5.8 (2)°. In the crystal, the mol­ecules are packed in a classic herringbone arrangement ty...

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Detalles Bibliográficos
Autores principales: Shotonwa, Ibukun O., Boeré, René T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515218/
https://www.ncbi.nlm.nih.gov/pubmed/23284438
http://dx.doi.org/10.1107/S1600536812039554
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author Shotonwa, Ibukun O.
Boeré, René T.
author_facet Shotonwa, Ibukun O.
Boeré, René T.
author_sort Shotonwa, Ibukun O.
collection PubMed
description In the structure of the title compound [systematic name: 1-(naphthalen-2-yl)ethanone], C(12)H(10)O, the acetyl group is approximately coplanar with the naphthalene ring with a C(ar)—C(ar)—C=O torsion angle of 5.8 (2)°. In the crystal, the mol­ecules are packed in a classic herringbone arrangement typical for aromatic polycycles such as penta­cene. They are also linked by weak end-to-end C—H⋯O interactions along the ac diagonal.
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spelling pubmed-35152182013-01-02 2′-Acetonaphthone Shotonwa, Ibukun O. Boeré, René T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the structure of the title compound [systematic name: 1-(naphthalen-2-yl)ethanone], C(12)H(10)O, the acetyl group is approximately coplanar with the naphthalene ring with a C(ar)—C(ar)—C=O torsion angle of 5.8 (2)°. In the crystal, the mol­ecules are packed in a classic herringbone arrangement typical for aromatic polycycles such as penta­cene. They are also linked by weak end-to-end C—H⋯O interactions along the ac diagonal. International Union of Crystallography 2012-10-13 /pmc/articles/PMC3515218/ /pubmed/23284438 http://dx.doi.org/10.1107/S1600536812039554 Text en © Shotonwa and Boeré 2012 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
Shotonwa, Ibukun O.
Boeré, René T.
2′-Acetonaphthone
title 2′-Acetonaphthone
title_full 2′-Acetonaphthone
title_fullStr 2′-Acetonaphthone
title_full_unstemmed 2′-Acetonaphthone
title_short 2′-Acetonaphthone
title_sort 2′-acetonaphthone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515218/
https://www.ncbi.nlm.nih.gov/pubmed/23284438
http://dx.doi.org/10.1107/S1600536812039554
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