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N-(2-Ferrocenylethylidene)-4-(trifluoromethyl)aniline
The title compound, [Fe(C(5)H(5))(C(13)H(9)F(3)N)], was prepared by a condensation reaction from ferrocenylcarbaldehyde and 4-(trifluoromethyl)aniline. The cyclopentadienyl (Cp) rings are coplanar [dihedral angle = 1.4 (3)°] and the imine function is situated in the same plane. The aromatic subs...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969081/ https://www.ncbi.nlm.nih.gov/pubmed/21582394 http://dx.doi.org/10.1107/S1600536809011039 |
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author | Imhof, Wolfgang |
author_facet | Imhof, Wolfgang |
author_sort | Imhof, Wolfgang |
collection | PubMed |
description | The title compound, [Fe(C(5)H(5))(C(13)H(9)F(3)N)], was prepared by a condensation reaction from ferrocenylcarbaldehyde and 4-(trifluoromethyl)aniline. The cyclopentadienyl (Cp) rings are coplanar [dihedral angle = 1.4 (3)°] and the imine function is situated in the same plane. The aromatic substituent is bent out of the plane of the Cp ring to which the imine group is attached by 44.5 (4)°. The F atoms of the trifluoromethyl substituent are disordered [occupancies 0.52 (2)/0.48 (2)]. |
format | Text |
id | pubmed-2969081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29690812010-12-30 N-(2-Ferrocenylethylidene)-4-(trifluoromethyl)aniline Imhof, Wolfgang Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers The title compound, [Fe(C(5)H(5))(C(13)H(9)F(3)N)], was prepared by a condensation reaction from ferrocenylcarbaldehyde and 4-(trifluoromethyl)aniline. The cyclopentadienyl (Cp) rings are coplanar [dihedral angle = 1.4 (3)°] and the imine function is situated in the same plane. The aromatic substituent is bent out of the plane of the Cp ring to which the imine group is attached by 44.5 (4)°. The F atoms of the trifluoromethyl substituent are disordered [occupancies 0.52 (2)/0.48 (2)]. International Union of Crystallography 2009-03-28 /pmc/articles/PMC2969081/ /pubmed/21582394 http://dx.doi.org/10.1107/S1600536809011039 Text en © Wolfgang Imhof 2009 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 Imhof, Wolfgang N-(2-Ferrocenylethylidene)-4-(trifluoromethyl)aniline |
title |
N-(2-Ferrocenylethylidene)-4-(trifluoromethyl)aniline |
title_full |
N-(2-Ferrocenylethylidene)-4-(trifluoromethyl)aniline |
title_fullStr |
N-(2-Ferrocenylethylidene)-4-(trifluoromethyl)aniline |
title_full_unstemmed |
N-(2-Ferrocenylethylidene)-4-(trifluoromethyl)aniline |
title_short |
N-(2-Ferrocenylethylidene)-4-(trifluoromethyl)aniline |
title_sort | n-(2-ferrocenylethylidene)-4-(trifluoromethyl)aniline |
topic | Metal-Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969081/ https://www.ncbi.nlm.nih.gov/pubmed/21582394 http://dx.doi.org/10.1107/S1600536809011039 |
work_keys_str_mv | AT imhofwolfgang n2ferrocenylethylidene4trifluoromethylaniline |