Effect of Iodide on the pH-Controlled Hydrogenations of Diphenylacetylene and Cinnamaldehyde Catalyzed by Ru(II)-Sulfonated Triphenylphosphine Complexes in Aqueous–Organic Biphasic Systems

• Published in: Catalysts Vol. 12; no. 5; p. 518
• Main Authors: Kathó, Ágnes, Horváth, Henrietta H., Papp, Gábor, Joó, Ferenc
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.05.2022
• Subjects: Catalysts; Chemical reactions; Cinnamaldehyde; diphenylacetylene; homogeneous catalysis; Hydrides; Hydrogenation; NMR; Nuclear magnetic resonance; pH-control; ruthenium; Selectivity; Sodium; Sodium salts; Stilbene; sulfonated triphenylphosphine
• ISSN: 2073-4344; 2073-4344
• DOI: 10.3390/catal12050518

The effect of NaI on hydrogenation of diphenylacetylene catalyzed by the water-soluble [{RuCl(mtppms-Na)2}2(µ-Cl)2] (1) (mtppms-Na = meta-monosulfonated triphenylphosphine sodium salt) is reported. Hydrogenations were performed under mild conditions (P(H2) = 1 bar, T = 50–80 ℃) in aqueous–organic biphasic reaction mixtures wherein the catalyst was dissolved in aqueous phase of various pHs. In acidic solutions, addition of NaI to 1 + mtppms-Na increased the selective conversion of diphenylacetylene to stilbenes from 10% to 90% but did not effect the high Z-selectivity (up to 98%). In contrast, in basic solutions the major product was diphenylethane (up to 70%), and the yield of E-stilbene exceeded that of the Z-isomer. 1H and 31P NMR measurements revealed that depending on the absence or presence of NaI, the catalytically active Ru(II)-hydride species in acidic solutions was [RuHCl(mtppms-Na)3], 2, or [RuHI(mtppms-Na)3], 5, respectively, while in basic solutions, both 2 and 5 were hydrogenated further to yield the same hydride species, cis,fac-[RuH2(H2O)(mtppms-Na)3]. [RuHI(mtppms-Na)3] proved superior to [RuHCl(mtppms-Na)3] as a catalyst for the selective hydrogenation of cinnamaldehyde to dihydrocinamaldehyde. This finding was explained by a facile formation of a (putative) dihydrogen complex [Ru(H2)I2(H2O)(mtppms-Na)2] intermediate, resulting in fast heterolytic activation of H2.