Autor: |
Florian Nährig, Yu Sun, Werner R. Thiel |
Jazyk: |
angličtina |
Rok vydání: |
2023 |
Předmět: |
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Zdroj: |
Chemistry, Vol 5, Iss 2, Pp 912-933 (2023) |
Druh dokumentu: |
article |
ISSN: |
2624-8549 |
DOI: |
10.3390/chemistry5020062 |
Popis: |
Simple nucleophilic aliphatic substitution gives access to mono- and diphosphine ligands with a CpC group in the backbone. The monophosphine ligand coordinates to gold(I) via the phosphine site, to thallium(I) via the cyclopentadienyl site and to ruthenium(II) via a combination of both, resulting in an ansa-type structure. Coordination with the cyclopentadiene site is not possible for the diphosphine ligand. In this case, monodentate coordination to gold(I) and bidentate coordination to the [PdCl(μ2-Cl)]2, the [Rh(CO)(μ2-Cl)]2, and the Rh(CO)Cl fragment is observed, showing the variability in coordination modes possible for the long-chain diphosphine ligand. Ligands and complexes were characterized by means of NMR and IR spectroscopy, elemental analysis and X-ray structure analysis. |
Databáze: |
Directory of Open Access Journals |
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