2-Ferrocenyl-3-nitro-2H-chromene

In the title compound, [Fe(C(5)H(5))(C(14)H(10)NO(3))], the cyclo­penta­dienyl rings are in an eclipsed conformation and the pyran ring adopts a half-chair conformation. The mean plane of the pyran ring makes dihedral angles of 79.33 (1) and 80.73 (1)°, respectively, with the substituted and unsubst...

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Autores principales: Paramasivam, S., Naga Siva Rao, Jonnalagadda, Seshadri, P. R., Raghunathan, Raghavachary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Metal-Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772416/
https://www.ncbi.nlm.nih.gov/pubmed/24046559
http://dx.doi.org/10.1107/S1600536813015730
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author Paramasivam, S.
Naga Siva Rao, Jonnalagadda
Seshadri, P. R.
Raghunathan, Raghavachary
author_facet Paramasivam, S.
Naga Siva Rao, Jonnalagadda
Seshadri, P. R.
Raghunathan, Raghavachary
author_sort Paramasivam, S.
collection PubMed
description In the title compound, [Fe(C(5)H(5))(C(14)H(10)NO(3))], the cyclo­penta­dienyl rings are in an eclipsed conformation and the pyran ring adopts a half-chair conformation. The mean plane of the pyran ring makes dihedral angles of 79.33 (1) and 80.73 (1)°, respectively, with the substituted and unsubstituted cyclo­penta­dienyl rings. In the crystal, pairs of C—H⋯O hydrogen bonds link the mol­ecules into inversion dimers with R (2) (2)(16) motifs.
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spelling pubmed-37724162013-09-17 2-Ferrocenyl-3-nitro-2H-chromene Paramasivam, S. Naga Siva Rao, Jonnalagadda Seshadri, P. R. Raghunathan, Raghavachary Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers In the title compound, [Fe(C(5)H(5))(C(14)H(10)NO(3))], the cyclo­penta­dienyl rings are in an eclipsed conformation and the pyran ring adopts a half-chair conformation. The mean plane of the pyran ring makes dihedral angles of 79.33 (1) and 80.73 (1)°, respectively, with the substituted and unsubstituted cyclo­penta­dienyl rings. In the crystal, pairs of C—H⋯O hydrogen bonds link the mol­ecules into inversion dimers with R (2) (2)(16) motifs. International Union of Crystallography 2013-06-12 /pmc/articles/PMC3772416/ /pubmed/24046559 http://dx.doi.org/10.1107/S1600536813015730 Text en © Paramasivam et al. 2013 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 Metal-Organic Papers
Paramasivam, S.
Naga Siva Rao, Jonnalagadda
Seshadri, P. R.
Raghunathan, Raghavachary
2-Ferrocenyl-3-nitro-2H-chromene
title 2-Ferrocenyl-3-nitro-2H-chromene
title_full 2-Ferrocenyl-3-nitro-2H-chromene
title_fullStr 2-Ferrocenyl-3-nitro-2H-chromene
title_full_unstemmed 2-Ferrocenyl-3-nitro-2H-chromene
title_short 2-Ferrocenyl-3-nitro-2H-chromene
title_sort 2-ferrocenyl-3-nitro-2h-chromene
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772416/
https://www.ncbi.nlm.nih.gov/pubmed/24046559
http://dx.doi.org/10.1107/S1600536813015730
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AT raghunathanraghavachary 2ferrocenyl3nitro2hchromene

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