http://www.cnr.it/ontology/cnr/individuo/prodotto/ID17071

Imidazolyl PTA Derivatives as Water Soluble (P,N) Ligands for Ru-catalysed Hydrogenations (Articolo in rivista)

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Imidazolyl PTA Derivatives as Water Soluble (P,N) Ligands for Ru-catalysed Hydrogenations (Articolo in rivista) (literal)

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Krogstad, Donald A.; Guerriero. Antonella; Ienco, Andrea; Manca, Gabriele; Peruzzini, Maurizio; Reginato, Gianna; Gonsalvi, Luca (2011)
Imidazolyl PTA Derivatives as Water Soluble (P,N) Ligands for Ru-catalysed Hydrogenations
in Organometallics; ACS, American chemical society, Washington, DC (Stati Uniti d'America)
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Krogstad, Donald A.; Guerriero. Antonella; Ienco, Andrea; Manca, Gabriele; Peruzzini, Maurizio; Reginato, Gianna; Gonsalvi, Luca (literal)

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Titolo

Imidazolyl PTA Derivatives as Water Soluble (P,N) Ligands for Ru-catalysed Hydrogenations (literal)

Abstract

The first imidazolyl \"upper-rim\" derivatives of 1,3,5-triaza-7-phoshaadamantane (PTA), namely, 1-methylimidazolyl-(1,3,5-triaza-7-phosphatricyclo[3.3.1.13,7]dec-6-yl)methanol (2, PTA-CH(1-MeIm)OH) and bis(1-methylimidazolyl)(1,3,5-triaza-7-phosphatricyclo[3.3.1.13,7]dec-6-yl)methanol (3, PTAC(1-MeIm)2OH), were synthesized in fair yields by reaction of PTA-Li with 1-methyl-2-imidazole carboxyaldehyde and bis-(N-methylimidazole-2-yl) ketone, respectively. Compounds 2 and 3 exhibit higher water solubility than most upper-rim derivatives of PTA. The two ligands reacted cleanly with [Ru(? 6-p-cymene)Cl2]2 in refluxing CHCl3 to form ? 2-P,N- [(? 6-p-cymene)Ru{PTA-CH(1-MeIm)OH}Cl]Cl (8) and ? 2-P,N-[(? 6-p-cymene)Ru{PTA-C(1-MeIm)2OH}Cl]Cl (9). Ligands phenyl(1,3,5-triaza-7-phosphatricyclo[3.3.1.13,7]dec-6-yl)-methanol (PZA) and 4?-dimethylaminophenyl(1,3,5-triaza-7-phosphatricyclo[3.3.1.13,7]dec-6-yl)methanol (PZA-NMe2) were also used to coordinate to Ru, and the corresponding ? 1-P-[(? 6-p-cymene)Ru(PZA)Cl2] (6) and ? 1-P-[(?6-p-cymene)Ru(PZANMe2) Cl2] (7) were isolated and characterized. The ability of the ligands to coordinate in ? 1-P vs ? 2-P,E (E = O, N) modes was established by NMR experiments and complemented by DFT calculations. The X-ray crystal structure of the iodide analogue of 7 was obtained. Complexes 6-9 were tested as catalysts for acetophenone reduction using different hydrogen sources under mild conditions, and preliminary results are here described. (literal)

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