We have recently reported the previously
unknown synthesis of thioesters
by coupling thiols and alcohols (or aldehydes) with liberation of
H
2
, as well as the reverse hydrogenation of thioesters,
catalyzed by a well-defined ruthenium acridine-9H based pincer complex.
These reactions are highly selective and are not deactivated by the
strongly coordinating thiols. Herein, the mechanism of this reversible
transformation is investigated in detail by a combined experimental
and computational (DFT) approach. We elucidate the likely pathway
of the reactions, and demonstrate experimentally how hydrogen gas
pressure governs selectivity toward hydrogenation or dehydrogenation.
With respect to the dehydrogenative process, we discuss a competing
mechanism for ester formation, which despite being thermodynamically
preferable, it is kinetically inhibited due to the relatively high
acidity of thiol compared to alcohol and, accordingly, the substantial
difference in the relative stabilities of a ruthenium thiolate intermediate
as opposed to a ruthenium alkoxide intermediate. Accordingly, various
additional reaction pathways were considered and are discussed herein,
including the dehydrogenative coupling of alcohol to ester and the
Tischenko reaction coupling aldehyde to ester. This study should inform
future green, (de)hydrogenative catalysis with thiols and other transformations
catalyzed by related ruthenium pincer complexes.