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2,8-Dimethyl-10-p-tolyl-10H-phenoxaphosphine
The title compound (systematic name: 3,6-dimethyl-10-p-tolyl-9-oxa-10-phosphaanthracene), C(21)H(19)OP, is a precursor for the preparation of a bidentate xanthene-based ligand, in which the dihedral angle between the toluene ring and the phenoxaphosphine ring system is 83.26 (3)°. The geometry at th...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968818/ https://www.ncbi.nlm.nih.gov/pubmed/21582548 http://dx.doi.org/10.1107/S1600536809009817 |
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author | Marimuthu, Thashree Bala, Muhammad D. Friedrich, Holger B. |
author_facet | Marimuthu, Thashree Bala, Muhammad D. Friedrich, Holger B. |
author_sort | Marimuthu, Thashree |
collection | PubMed |
description | The title compound (systematic name: 3,6-dimethyl-10-p-tolyl-9-oxa-10-phosphaanthracene), C(21)H(19)OP, is a precursor for the preparation of a bidentate xanthene-based ligand, in which the dihedral angle between the toluene ring and the phenoxaphosphine ring system is 83.26 (3)°. The geometry at the P atom is pyramidal, resulting in a longer C—P bond length as compared to the two ring C—P bonds. |
format | Text |
id | pubmed-2968818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29688182010-12-30 2,8-Dimethyl-10-p-tolyl-10H-phenoxaphosphine Marimuthu, Thashree Bala, Muhammad D. Friedrich, Holger B. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound (systematic name: 3,6-dimethyl-10-p-tolyl-9-oxa-10-phosphaanthracene), C(21)H(19)OP, is a precursor for the preparation of a bidentate xanthene-based ligand, in which the dihedral angle between the toluene ring and the phenoxaphosphine ring system is 83.26 (3)°. The geometry at the P atom is pyramidal, resulting in a longer C—P bond length as compared to the two ring C—P bonds. International Union of Crystallography 2009-03-25 /pmc/articles/PMC2968818/ /pubmed/21582548 http://dx.doi.org/10.1107/S1600536809009817 Text en © Marimuthu et al. 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 | Organic Papers Marimuthu, Thashree Bala, Muhammad D. Friedrich, Holger B. 2,8-Dimethyl-10-p-tolyl-10H-phenoxaphosphine |
title | 2,8-Dimethyl-10-p-tolyl-10H-phenoxaphosphine |
title_full | 2,8-Dimethyl-10-p-tolyl-10H-phenoxaphosphine |
title_fullStr | 2,8-Dimethyl-10-p-tolyl-10H-phenoxaphosphine |
title_full_unstemmed | 2,8-Dimethyl-10-p-tolyl-10H-phenoxaphosphine |
title_short | 2,8-Dimethyl-10-p-tolyl-10H-phenoxaphosphine |
title_sort | 2,8-dimethyl-10-p-tolyl-10h-phenoxaphosphine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968818/ https://www.ncbi.nlm.nih.gov/pubmed/21582548 http://dx.doi.org/10.1107/S1600536809009817 |
work_keys_str_mv | AT marimuthuthashree 28dimethyl10ptolyl10hphenoxaphosphine AT balamuhammadd 28dimethyl10ptolyl10hphenoxaphosphine AT friedrichholgerb 28dimethyl10ptolyl10hphenoxaphosphine |