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Title: Hydrogen chemistry of ruthenium complexes containing one chelating (P-P) or (P-N) ligand per Ru atom

Conference ·
OSTI ID:126651
 [1]
  1. Univ. of British Columbia, Vancouver (Canada)

Hydrogenation catalysts are of interest to a variety of fields such as fuels preparation. This report describes a hydrogenation catalysts concerning ruthenium. The most versatile hydrogenation catalysts appear to be based on Ru(P-P) species containing one chelating ditertiaryphosphine(P-P) ligand per metal, particularly for asymmetric hydrogenation when (P-P) is chiral. We have studied the interaction of H{sub 2} with, and catalytic hydrogenation activity (toward olefins ketones, nitrites and imines) of, systems containing the {open_quote}RuCl{sub 2}(P-P){close_quote} moiety or corresponding chelating (P-N) ligands where N is a tertiary amine. Variation in conditions leads to detection or isolation of, for example, ({eta}{sup 2}-H{sub 2})(P-P)Ru({mu}-Cl){sub 3}RuCl(P-P) (1), ({eta}{sup 2}-H{sub 2})(P-P)Ru({mu}-Cl){sub 2}({mu}-H)Ru(H)(P-P) (2), and [Ru(H)Cl(P-P)]{sub 3} (3), as well as analogous species where the {eta}{sup 2}-H{sub 2} of 1 or 2 is replaced by olefin, ketone, nitrile, or imine. The connectivity between 1-3, and kinetic and mechanistic details of selected catalytic hydrogenations will be discussed. Within (P-N) systems, the mononuclear species ({eta}{sup 2}-H{sub 2})RuCl{sub 2}(P-N)(PR{sub 3}) and Ru(H)Cl(P-N)(PR{sub 3}) are formed (R = Ph or p-tolyl), as well as species analogous to 2.

OSTI ID:
126651
Report Number(s):
CONF-950402-; TRN: 95:006086-0636
Resource Relation:
Conference: 209. American Chemical Society (ACS) national meeting, Anaheim, CA (United States), 2-6 Apr 1995; Other Information: PBD: 1995; Related Information: Is Part Of 209th ACS national meeting; PB: 2088 p.
Country of Publication:
United States
Language:
English