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Synthesis and characterization of TADDOL-based chiral group six PNP pincer tricarbonyl complexes
ABSTRACT: The new chiral PNP pincer ligand N(2),N(6)-bis((3aR, 8aR)-2,2-dimethyl-4,4,8,8-tetraphenyltetrahydro[1,3]dioxolo[4,5-e][1,3,2]dioxaphosphepin-6-yl)pyridine-2,6-diamine (PNP-TADDOL) was synthesized in 80% isolated yield. Complexes of the type [M(PNP-TADDOL)(CO)(3)] (M = Cr, Mo, and W) were...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320742/ https://www.ncbi.nlm.nih.gov/pubmed/30662092 http://dx.doi.org/10.1007/s00706-018-2281-0 |
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author | de Aguiar, Sara R. M. M. Schröder-Holzhacker, Christian Pecak, Jan Stöger, Berthold Kirchner, Karl |
author_facet | de Aguiar, Sara R. M. M. Schröder-Holzhacker, Christian Pecak, Jan Stöger, Berthold Kirchner, Karl |
author_sort | de Aguiar, Sara R. M. M. |
collection | PubMed |
description | ABSTRACT: The new chiral PNP pincer ligand N(2),N(6)-bis((3aR, 8aR)-2,2-dimethyl-4,4,8,8-tetraphenyltetrahydro[1,3]dioxolo[4,5-e][1,3,2]dioxaphosphepin-6-yl)pyridine-2,6-diamine (PNP-TADDOL) was synthesized in 80% isolated yield. Complexes of the type [M(PNP-TADDOL)(CO)(3)] (M = Cr, Mo, and W) were prepared via a solvothermal approach. This methodology constitutes a fast, simple, and practical synthetic method to obtain complexes of that type in high isolated yields. The X-ray structure of the molybdenum complex is presented. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-6320742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-63207422019-01-17 Synthesis and characterization of TADDOL-based chiral group six PNP pincer tricarbonyl complexes de Aguiar, Sara R. M. M. Schröder-Holzhacker, Christian Pecak, Jan Stöger, Berthold Kirchner, Karl Monatsh Chem Original Paper ABSTRACT: The new chiral PNP pincer ligand N(2),N(6)-bis((3aR, 8aR)-2,2-dimethyl-4,4,8,8-tetraphenyltetrahydro[1,3]dioxolo[4,5-e][1,3,2]dioxaphosphepin-6-yl)pyridine-2,6-diamine (PNP-TADDOL) was synthesized in 80% isolated yield. Complexes of the type [M(PNP-TADDOL)(CO)(3)] (M = Cr, Mo, and W) were prepared via a solvothermal approach. This methodology constitutes a fast, simple, and practical synthetic method to obtain complexes of that type in high isolated yields. The X-ray structure of the molybdenum complex is presented. GRAPHICAL ABSTRACT: [Image: see text] Springer Vienna 2018-10-20 2019 /pmc/articles/PMC6320742/ /pubmed/30662092 http://dx.doi.org/10.1007/s00706-018-2281-0 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper de Aguiar, Sara R. M. M. Schröder-Holzhacker, Christian Pecak, Jan Stöger, Berthold Kirchner, Karl Synthesis and characterization of TADDOL-based chiral group six PNP pincer tricarbonyl complexes |
title | Synthesis and characterization of TADDOL-based chiral group six PNP pincer tricarbonyl complexes |
title_full | Synthesis and characterization of TADDOL-based chiral group six PNP pincer tricarbonyl complexes |
title_fullStr | Synthesis and characterization of TADDOL-based chiral group six PNP pincer tricarbonyl complexes |
title_full_unstemmed | Synthesis and characterization of TADDOL-based chiral group six PNP pincer tricarbonyl complexes |
title_short | Synthesis and characterization of TADDOL-based chiral group six PNP pincer tricarbonyl complexes |
title_sort | synthesis and characterization of taddol-based chiral group six pnp pincer tricarbonyl complexes |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320742/ https://www.ncbi.nlm.nih.gov/pubmed/30662092 http://dx.doi.org/10.1007/s00706-018-2281-0 |
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