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5,15-Bis(4-pentyloxyphenyl)porphyrin
In the title compound, C(42)H(42)N(4)O(2), the complete molecule is generated by a crystallographic inversion centre. The porphyrin system exhibits a near planar macrocycle conformation with an average deviation from the least-squares plane of the 24 macrocycle atoms of 0.037 (5) Å. The phenyl ipso...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772480/ https://www.ncbi.nlm.nih.gov/pubmed/24046623 http://dx.doi.org/10.1107/S160053681301550X |
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author | Senge, Mathias O. |
author_facet | Senge, Mathias O. |
author_sort | Senge, Mathias O. |
collection | PubMed |
description | In the title compound, C(42)H(42)N(4)O(2), the complete molecule is generated by a crystallographic inversion centre. The porphyrin system exhibits a near planar macrocycle conformation with an average deviation from the least-squares plane of the 24 macrocycle atoms of 0.037 (5) Å. The phenyl ipso C atoms are positioned above and below the porphyrin plane by 0.35 (1) Å and the macrocycle shows evidence of in-plane rectangular elongation with N⋯N separations of 3.032 (5) and 2.803 (5) Å. Two intramolecular N—H⋯N hydrogen bonds occur. |
format | Online Article Text |
id | pubmed-3772480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-37724802013-09-17 5,15-Bis(4-pentyloxyphenyl)porphyrin Senge, Mathias O. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(42)H(42)N(4)O(2), the complete molecule is generated by a crystallographic inversion centre. The porphyrin system exhibits a near planar macrocycle conformation with an average deviation from the least-squares plane of the 24 macrocycle atoms of 0.037 (5) Å. The phenyl ipso C atoms are positioned above and below the porphyrin plane by 0.35 (1) Å and the macrocycle shows evidence of in-plane rectangular elongation with N⋯N separations of 3.032 (5) and 2.803 (5) Å. Two intramolecular N—H⋯N hydrogen bonds occur. International Union of Crystallography 2013-06-08 /pmc/articles/PMC3772480/ /pubmed/24046623 http://dx.doi.org/10.1107/S160053681301550X Text en © Mathias O. Senge 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 | Organic Papers Senge, Mathias O. 5,15-Bis(4-pentyloxyphenyl)porphyrin |
title | 5,15-Bis(4-pentyloxyphenyl)porphyrin |
title_full | 5,15-Bis(4-pentyloxyphenyl)porphyrin |
title_fullStr | 5,15-Bis(4-pentyloxyphenyl)porphyrin |
title_full_unstemmed | 5,15-Bis(4-pentyloxyphenyl)porphyrin |
title_short | 5,15-Bis(4-pentyloxyphenyl)porphyrin |
title_sort | 5,15-bis(4-pentyloxyphenyl)porphyrin |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772480/ https://www.ncbi.nlm.nih.gov/pubmed/24046623 http://dx.doi.org/10.1107/S160053681301550X |
work_keys_str_mv | AT sengemathiaso 515bis4pentyloxyphenylporphyrin |