TY - JOUR
T1 - Study of Precatalyst Degradation Leading to the Discovery of a New Ru0 Precatalyst for Hydrogenation and Dehydrogenation
AU - Anaby, Aviel
AU - Schelwies, Mathias
AU - Schwaben, Jonas
AU - Rominger, Frank
AU - Hashmi, A. Stephen K.
AU - Schaub, Thomas
N1 - Publisher Copyright:
Copyright © 2018 American Chemical Society.
PY - 2018/7/9
Y1 - 2018/7/9
N2 - The complex Ru-MACHO (1) is a widely used precatalyst for hydrogenation and dehydrogenation reactions under basic conditions. In an attempt to identify the active catalyst form, 1 was reacted with a strong base. The formation of previously unreported species was observed by NMR and mass spectrometry. This observation indicated that complex 1 quickly degraded under basic conditions when no substrate was present. X-ray crystallography enabled the identification of three complexes as products of this degradation of complex 1. These complexes suggested degradation pathways which included ligand cleavage and reassembly, along with reduction of the ruthenium atom. One of the decomposition products, the Ru0 complex [Ru(N(CH2CH2PPh2)3)CO] (5), was prepared independently and studied. 5 was found to be active, entirely additive-free, in the acceptorless dehydrogenation of aliphatic alcohols to esters. The hydrogenation of esters catalyzed by 5 was also demonstrated under base-free conditions with methanol as an additive. Protic substrates were shown to add reversibly to complex 5, generating RuII-hydrido species, thus presenting a rare example of reversible oxidative addition from Ru0 to RuII and reductive elimination from RuII to Ru0.
AB - The complex Ru-MACHO (1) is a widely used precatalyst for hydrogenation and dehydrogenation reactions under basic conditions. In an attempt to identify the active catalyst form, 1 was reacted with a strong base. The formation of previously unreported species was observed by NMR and mass spectrometry. This observation indicated that complex 1 quickly degraded under basic conditions when no substrate was present. X-ray crystallography enabled the identification of three complexes as products of this degradation of complex 1. These complexes suggested degradation pathways which included ligand cleavage and reassembly, along with reduction of the ruthenium atom. One of the decomposition products, the Ru0 complex [Ru(N(CH2CH2PPh2)3)CO] (5), was prepared independently and studied. 5 was found to be active, entirely additive-free, in the acceptorless dehydrogenation of aliphatic alcohols to esters. The hydrogenation of esters catalyzed by 5 was also demonstrated under base-free conditions with methanol as an additive. Protic substrates were shown to add reversibly to complex 5, generating RuII-hydrido species, thus presenting a rare example of reversible oxidative addition from Ru0 to RuII and reductive elimination from RuII to Ru0.
UR - http://www.scopus.com/inward/record.url?scp=85049756492&partnerID=8YFLogxK
U2 - 10.1021/acs.organomet.8b00353
DO - 10.1021/acs.organomet.8b00353
M3 - Article
AN - SCOPUS:85049756492
SN - 0276-7333
VL - 37
SP - 2193
EP - 2201
JO - Organometallics
JF - Organometallics
IS - 13
ER -