AUTHOR=Ocansey Edward , Darkwa James , Makhubela Banothile C. E. TITLE=Chiral-at-Metal: Iridium(III) Tetrazole Complexes With Proton-Responsive P-OH Groups for CO2 Hydrogenation JOURNAL=Frontiers in Chemistry VOLUME=8 YEAR=2020 URL=https://www.frontiersin.org/journals/chemistry/articles/10.3389/fchem.2020.591353 DOI=10.3389/fchem.2020.591353 ISSN=2296-2646 ABSTRACT=

A rise in atmospheric CO₂ levels, following years of burning fossil fuels, has brought about increase in global temperatures and climate change due to the greenhouse effect. As such, recent efforts in addressing this problem have been directed to the use of CO₂ as a non-expensive and non-toxic single carbon, C₁, source for making chemical products. Herein, we report on the use of tetrazolyl complexes as catalyst precursors for hydrogenation of CO₂. Specifically, tetrazolyl compounds bearing P–S bonds have been synthesized with the view of using these as P^∧N bidentate tetrazolyl ligands (1–3) that can coordinate to iridium(III), thereby forming heteroatomic five-member complexes. Interestingly, reacting the P,N′-bidentate tetrazolyl ligands with [Ir(_{C₅Me₅)Cl₂]2} led to serendipitous isolation of chiral-at-metal iridium(III) half-sandwich complexes (7–9) instead. Complexes 7–9 were obtained via prior formation of non-chiral iridium(III) half-sandwich complexes (4–6). The complexes undergo prior P–S bond heterolysis of the precursor ligands, which then ultimately results in new half-sandwich iridium(III) complexes featuring monodentate phosphine co-ligands with proton-responsive P-OH groups. Conditions necessary to significantly affect the rate of P–S bond heterolysis in the precursor ligand and the subsequent coordination to iridium have been reported. The complexes served as catalyst precursors and exhibited activity in CO₂ and bicarbonate hydrogenation in excellent catalytic activity, at low catalyst loadings (1 μmol or 0.07 mol% with respect to base), producing concentrated formate solutions (ca 180 mM) exclusively. Catalyst precursors with proton-responsive P-OH groups were found to influence catalytic activity when present as racemates, while ease of dissociation of the ligand from the iridium center was observed to influence activity in spite of the presence of electron-donating ligands. A test for homogeneity indicated that hydrogenation of CO₂ proceeded by homogeneous means. Subsequently, the mechanism of the reaction by the iridium(III) catalyst precursors was studied using ¹H NMR techniques. This revealed that a chiral-at-metal iridium hydride species generated in situ served as the active catalyst.