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Hashimoto T., Asada T., Ogoshi S., et al. Main group catalysis for H2 purification based on liquid organic hydrogen carriers. Science Advances 8, eade0189 (2022); https://doi.org/10.1126/sciadv.ade0189., Molecular hydrogen (H2) is one of the most important energy carriers. In the midterm future, a huge amount of H2 will be produced from a variety of hydrocarbon sources through conversion and removal of contaminants such as CO and CO2. However, bypassing these purification processes is desirable, given their energy consumption and environmental impact, which ultimately increases the cost of H2. Here, we demonstrate a strategy to separate H2 from a gaseous mixture of H2/CO/CO2/CH4 that can include an excess of CO and CO2 relative to H2 and simultaneously store it in N-heterocyclic compounds that act as liquid organic hydrogen carriers (LOHCs), which can be applied to produce H2 by subsequent dehydrogenation. Our results demonstrate that LOHCs can potentially be used for H2 purification from CO- and CO2-rich crude H2 in addition to their well-established use in H2 storage.

Yamauchi Y., Hoshimoto Y., Kawakita T., et al. Room-Temperature Reversible Chemisorption of Carbon Monoxide on Nickel(0) Complexes. Journal of the American Chemical Society , (2022); https://doi.org/10.1021/jacs.2c02870., Chemisorption on organometallic-based adsorbents is crucial for the controlled separation and long-term storage of gaseous molecules. The formation of covalent bonds between the metal centers in the adsorbents and the targeted gases affects the desorption efficiency, especially when the oxidation state of the metal is low. Herein, we report a pressure-responsive nickel(0)-based system that is able to reversibly chemisorb carbon monoxide (CO) at room temperature. The use of N-heterocyclic carbene ligands with hemi-labile N-phosphine oxide substituents facilitates both the adsorption and desorption of CO on nickel(0) via ligand substitution. Ionic liquids were used as the reaction medium to enhance the desorption rate and establish a reusable system. These results showcase a way for the sustainable chemisorption of CO using a zero-valent transition-metal complex.

Chemists have designed strategies that trigger the conformational isomerization of molecules in response to external stimuli, which can be further applied to regulate the complexation between Lewis acids and bases. We have recently developed a system in which frustrated carbene-borane pairs are revived from shelf-stable but external-stimuli-responsive carbene-borane adducts comprised of N-phosphine-oxide-substituted imidazolylidenes (PoxIms) and triarylboranes. Herein, we report the detailed mechanism on this revival process. A thermally induced borane-transfer process from the carbene carbon atom to the N-phosphinoyl oxygen atom initiates the transformation of the carbene-borane adduct. Subsequent conformational isomerization via the rotation of the N-phosphinoyl group in PoxIm moieties eventually leads to the revival of frustrated carbene-borane pairs that can cleave H-2. We believe that this work illustrates an essential role of dynamic conformational isomerization in the regulation of the reactivity of external-stimuli-responsive Lewis acid-base adducts that contain multifunctional substituents. Frustrated Lewis pairs can be thermally revived from classical Lewis adducts, but the mechanism by which this occurs is not well understood. Here a combined experimental and theoretical study supports a pathway mediated by boron-jumping and dynamic conformational isomerization.

Asada T., Hoshimoto Y., Ogoshi S.. Rotation-Triggered Transmetalation on a Heterobimetallic Cu/Al N-Phosphine-Oxide-Substituted Imidazolylidene Complex. Journal of the American Chemical Society 142, 9772 (2020); https://doi.org/10.1021/jacs.0c03252., A novel strategy for the preparation of heterobimetallic N-heterocyclic carbene (NHC) complexes is demonstrated using N-phosphine-oxide-substituted imidazolylidenes (PoxIms). In these heterobimetallic Cu/Al complexes, the Cu and Al centers can be either completely separated or brought near each other via the rotation of the N-phosphinoyl group in the PoxIm ligands. Triggered by this rotation, transmetalation to exchange the Cu-OtBu and Al-C6F5 bonds occurs on in situ-generated Cu/Al PoxIm complexes, and the Cu-C6F5 and Al-OtBu bonds are formed in excellent yield. On the basis of the results of mechanistic studies, including the isolation/in situ observation of key complexes and theoretical calculations, a plausible reaction mechanism for an intramolecular transmetalation is proposed to proceed via an activation complex that includes the simultaneous coordination of the phosphinoyl oxygen atom to the Cu as well as the Al centers. Furthermore, the formation of carbon-carbon bonds between Al(C6F5)3 and allyl bromide mediated/catalyzed by Cu/Al PoxIm complexes is demonstrated. Upon the consecutive transfer of three C6F5 groups from a single molecule of Al(C6F5)3, allyl pentafluorobenzene derivatives were obtained. The present results demonstrate the role of phosphine oxide in the activation of organoaluminum reagents for the transmetalation between Cu(I) complexes bearing NHCs as well as the benefit of constructing an intramolecular system based on a heterobimetallic complex to achieve efficient transmetalation by programming the encounter of two organometallic fragments.

Hazra S., Hoshimoto Y., Ogoshi S.. N-Phosphine Oxide-Substituted Imidazolylidenes (PoxIms): Multifunctional Multipurpose Carbenes. Chemistry - A European Journal 23, 15238 (2017); https://doi.org/10.1002/chem.201703644., This article discusses the concept of N-heterocyclic carbenes (NHCs) equipped with more than one functional moiety, which allows using these NHCs for multiple purposes. A pioneering example for such NHCs is N-phosphine oxide-substituted imidazolylidenes (PoxIms), and their synthesis and strategic use are highlighted. The utility of PoxIms by far exceeds the conventional use as multidentate ligands for metal complexes on account of the synergetic functions of the carbene and the N-phosphine oxide group(s).