HCOOH disproportionation to MeOH promoted by molybdenum PNP complexes
Elisabetta Alberico, Thomas Leischner, Henrik Junge, Anja Kammer, Rui Sang, Jenny Seifert, Wolfgang Baumann, Anke Spannenberg, Kathrin Junge, Matthias Beller
Abstract
Molybdenum(0) complexes with aliphatic aminophosphine pincer ligands have been prepared which are competent for the disproportionation of formic acid, thus representing the first example so far reported of non-noble metal species to catalytically promote such transformation. In general, formic acid disproportionation allows for an alternative access to methyl formate and methanol from renewable resources. MeOH selectivity up to 30% with a TON of 57 could be achieved while operating at atmospheric pressure. Selectivity (37%) and catalyst performance (TON = 69) could be further enhanced when the reaction was performed under hydrogen pressure (60 bars). A plausible mechanism based on experimental evidence is proposed.