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Minor Modifications to the Ligands Surrounding a Ruthenium Complex Lead to Major Differences in the Way in which they Catalyse the Hydrogenation of Arenes
Author(s) -
Dyson Paul J.,
Ellis David J.,
Laurenczy Gábor
Publication year - 2003
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.200390014
Subject(s) - tppts , chemistry , ruthenium , catalysis , medicinal chemistry , hydroformylation , benzene , salt (chemistry) , aqueous solution , organic chemistry , rhodium
The hydrogenation of benzene and other arenes under aqueous‐organic biphasic conditions is evaluated using the ruthenium complexes Ru(η 6 ‐C 10 H 14 )(pta)Cl 2 (pta=1,3,5‐triaza‐7‐phosphaadamantane), Ru(η 6 ‐C 10 H 14 )(tppts)Cl 2 (tppts=tris‐3‐sulfonatophenylphosphine trisodium salt) and [Ru(η 6 ‐C 10 H 14 )(pta) 2 Cl] + . The active catalysts formed during the hydrogenations correspond to a trinuclear cluster, a colloid and a mononuclear complex, respectively.

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