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Isolation of Au-, Co-η(1)PCO and Cu-η(2)PCO complexes, conversion of an Ir–η(1)PCO complex into a dimetalladiphosphene, and an interaction-free PCO anion
Sodium phosphaethynolate reacts with [MCl(PDI)] (M = Co, Ir; PDI = pyridinediimine) to give metallaphosphaketenes, which in the case of iridium rearranges into a dimetalladiphosphene, via CO migration from phosphorus to the metal. Two different bonding modes of the PCO anion to CAAC-coinage metal co...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003603/ https://www.ncbi.nlm.nih.gov/pubmed/29997776 http://dx.doi.org/10.1039/c5sc04504e |
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author | Liu, Liu Ruiz, David A. Dahcheh, Fatme Bertrand, Guy Suter, Riccardo Tondreau, Aaron M. Grützmacher, Hansjörg |
author_facet | Liu, Liu Ruiz, David A. Dahcheh, Fatme Bertrand, Guy Suter, Riccardo Tondreau, Aaron M. Grützmacher, Hansjörg |
author_sort | Liu, Liu |
collection | PubMed |
description | Sodium phosphaethynolate reacts with [MCl(PDI)] (M = Co, Ir; PDI = pyridinediimine) to give metallaphosphaketenes, which in the case of iridium rearranges into a dimetalladiphosphene, via CO migration from phosphorus to the metal. Two different bonding modes of the PCO anion to CAAC-coinage metal complexes [CAAC: cyclic (alkyl)(amino)(carbene)] are reported, one featuring a strong Au–P bond and the other an η(2) coordination to copper. The gold complex appears to be mostly unreactive whereas the copper complex readily reacts with various organic substrates. A completely free PCO anion was structurally characterized as the [Cu(L(a))(2)](+) (OCP)(–) salt. It results from the simple displacement of the PCO unit of the cationic (CAAC)Cu(PCO) complex by a second equivalent of CAAC. |
format | Online Article Text |
id | pubmed-6003603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-60036032018-07-11 Isolation of Au-, Co-η(1)PCO and Cu-η(2)PCO complexes, conversion of an Ir–η(1)PCO complex into a dimetalladiphosphene, and an interaction-free PCO anion Liu, Liu Ruiz, David A. Dahcheh, Fatme Bertrand, Guy Suter, Riccardo Tondreau, Aaron M. Grützmacher, Hansjörg Chem Sci Chemistry Sodium phosphaethynolate reacts with [MCl(PDI)] (M = Co, Ir; PDI = pyridinediimine) to give metallaphosphaketenes, which in the case of iridium rearranges into a dimetalladiphosphene, via CO migration from phosphorus to the metal. Two different bonding modes of the PCO anion to CAAC-coinage metal complexes [CAAC: cyclic (alkyl)(amino)(carbene)] are reported, one featuring a strong Au–P bond and the other an η(2) coordination to copper. The gold complex appears to be mostly unreactive whereas the copper complex readily reacts with various organic substrates. A completely free PCO anion was structurally characterized as the [Cu(L(a))(2)](+) (OCP)(–) salt. It results from the simple displacement of the PCO unit of the cationic (CAAC)Cu(PCO) complex by a second equivalent of CAAC. Royal Society of Chemistry 2016-03-01 2016-01-04 /pmc/articles/PMC6003603/ /pubmed/29997776 http://dx.doi.org/10.1039/c5sc04504e Text en This journal is © The Royal Society of Chemistry 2016 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Liu, Liu Ruiz, David A. Dahcheh, Fatme Bertrand, Guy Suter, Riccardo Tondreau, Aaron M. Grützmacher, Hansjörg Isolation of Au-, Co-η(1)PCO and Cu-η(2)PCO complexes, conversion of an Ir–η(1)PCO complex into a dimetalladiphosphene, and an interaction-free PCO anion |
title | Isolation of Au-, Co-η(1)PCO and Cu-η(2)PCO complexes, conversion of an Ir–η(1)PCO complex into a dimetalladiphosphene, and an interaction-free PCO anion
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title_full | Isolation of Au-, Co-η(1)PCO and Cu-η(2)PCO complexes, conversion of an Ir–η(1)PCO complex into a dimetalladiphosphene, and an interaction-free PCO anion
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title_fullStr | Isolation of Au-, Co-η(1)PCO and Cu-η(2)PCO complexes, conversion of an Ir–η(1)PCO complex into a dimetalladiphosphene, and an interaction-free PCO anion
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title_full_unstemmed | Isolation of Au-, Co-η(1)PCO and Cu-η(2)PCO complexes, conversion of an Ir–η(1)PCO complex into a dimetalladiphosphene, and an interaction-free PCO anion
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title_short | Isolation of Au-, Co-η(1)PCO and Cu-η(2)PCO complexes, conversion of an Ir–η(1)PCO complex into a dimetalladiphosphene, and an interaction-free PCO anion
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title_sort | isolation of au-, co-η(1)pco and cu-η(2)pco complexes, conversion of an ir–η(1)pco complex into a dimetalladiphosphene, and an interaction-free pco anion |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003603/ https://www.ncbi.nlm.nih.gov/pubmed/29997776 http://dx.doi.org/10.1039/c5sc04504e |
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