The palladium catalysed Pd-aryl/P-aryl exchange was applied in the synthesis of various functionalised phosphines from their corresponding substituted aryl triflates using triarylphosphines as the phosphinating agents. This method tolerated many functional groups including ketone, aldehyde, ester, n
Ditopic Ligands. The Synthesis of a Series of Phosphine-Functionalised Macrocycles
β Scribed by Annick Carroy; C. Richard Langick; Jean-Marie Lehn; Karen E. Matthes; David Parker
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- German
- Weight
- 498 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0018-019X
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β¦ Synopsis
The synthesis of a series of phosphine-functionalised macrocycles, 1 4 , is described. The combination of Nand O-sites with P-and S-sites provides ligands which may bind transition or non-transition metal ions; as a consequence, they give access to dinuclear complexes containing both a Lewis acid and a redox metallic site. Compounds 1,2 and 6 are heterodinucleating ligands capable of binding two dissimilar metals in proximity. Macrocycles >S are homotopic ligands which may form homodinuclear complexes of transition metals.
π SIMILAR VOLUMES
Chemistry is reported that allows for the synthesis and screening of phosphine ligands by standard combinatorial technology. To demonstrate the method, libraries of phosphine containing peptides were synthesized. Rhodium was complexed to the phosphine ligands while they were attached to the synthesi
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