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3′,6′-Bis(ethylamino)-2′,7′-dimethyl-2-{2-(E)-[(thiophen-2-yl)methylideneamino]ethyl}spiro[isoindoline-1,9′-xanthen]-3-one methanol monosolvate
The title compound, C(33)H(34)N(4)O(2)S·CH(3)OH, was prepared as a spirolactam ring formation of rhodamine 6 G dye for comparison with a ring-opened form. The xanthene and spirolactam rings are approximately planar [r.m.s. deviations from planarity = 0.122 (3) and 0.072 (6) Å, respectively]. The d...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344655/ https://www.ncbi.nlm.nih.gov/pubmed/22590417 http://dx.doi.org/10.1107/S1600536812018181 |
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author | Li, Qing-yu Guo, Rui Xu, Zhi-hong |
author_facet | Li, Qing-yu Guo, Rui Xu, Zhi-hong |
author_sort | Li, Qing-yu |
collection | PubMed |
description | The title compound, C(33)H(34)N(4)O(2)S·CH(3)OH, was prepared as a spirolactam ring formation of rhodamine 6 G dye for comparison with a ring-opened form. The xanthene and spirolactam rings are approximately planar [r.m.s. deviations from planarity = 0.122 (3) and 0.072 (6) Å, respectively]. The dihedral angles formed by the spirolactam and thiophene rings with the xanthene ring system are 89.7 (6) and 86.5 (2)°, respectively. The crystal structure features N—H⋯O and C—H⋯O hydrogen bonds. |
format | Online Article Text |
id | pubmed-3344655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33446552012-05-15 3′,6′-Bis(ethylamino)-2′,7′-dimethyl-2-{2-(E)-[(thiophen-2-yl)methylideneamino]ethyl}spiro[isoindoline-1,9′-xanthen]-3-one methanol monosolvate Li, Qing-yu Guo, Rui Xu, Zhi-hong Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(33)H(34)N(4)O(2)S·CH(3)OH, was prepared as a spirolactam ring formation of rhodamine 6 G dye for comparison with a ring-opened form. The xanthene and spirolactam rings are approximately planar [r.m.s. deviations from planarity = 0.122 (3) and 0.072 (6) Å, respectively]. The dihedral angles formed by the spirolactam and thiophene rings with the xanthene ring system are 89.7 (6) and 86.5 (2)°, respectively. The crystal structure features N—H⋯O and C—H⋯O hydrogen bonds. International Union of Crystallography 2012-04-28 /pmc/articles/PMC3344655/ /pubmed/22590417 http://dx.doi.org/10.1107/S1600536812018181 Text en © Li et al. 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 Li, Qing-yu Guo, Rui Xu, Zhi-hong 3′,6′-Bis(ethylamino)-2′,7′-dimethyl-2-{2-(E)-[(thiophen-2-yl)methylideneamino]ethyl}spiro[isoindoline-1,9′-xanthen]-3-one methanol monosolvate |
title | 3′,6′-Bis(ethylamino)-2′,7′-dimethyl-2-{2-(E)-[(thiophen-2-yl)methylideneamino]ethyl}spiro[isoindoline-1,9′-xanthen]-3-one methanol monosolvate |
title_full | 3′,6′-Bis(ethylamino)-2′,7′-dimethyl-2-{2-(E)-[(thiophen-2-yl)methylideneamino]ethyl}spiro[isoindoline-1,9′-xanthen]-3-one methanol monosolvate |
title_fullStr | 3′,6′-Bis(ethylamino)-2′,7′-dimethyl-2-{2-(E)-[(thiophen-2-yl)methylideneamino]ethyl}spiro[isoindoline-1,9′-xanthen]-3-one methanol monosolvate |
title_full_unstemmed | 3′,6′-Bis(ethylamino)-2′,7′-dimethyl-2-{2-(E)-[(thiophen-2-yl)methylideneamino]ethyl}spiro[isoindoline-1,9′-xanthen]-3-one methanol monosolvate |
title_short | 3′,6′-Bis(ethylamino)-2′,7′-dimethyl-2-{2-(E)-[(thiophen-2-yl)methylideneamino]ethyl}spiro[isoindoline-1,9′-xanthen]-3-one methanol monosolvate |
title_sort | 3′,6′-bis(ethylamino)-2′,7′-dimethyl-2-{2-(e)-[(thiophen-2-yl)methylideneamino]ethyl}spiro[isoindoline-1,9′-xanthen]-3-one methanol monosolvate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344655/ https://www.ncbi.nlm.nih.gov/pubmed/22590417 http://dx.doi.org/10.1107/S1600536812018181 |
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