Parahydrogen-induced polarization is a nuclear spin hyperpolarization technique that can provide strongly enhanced NMR signals for catalytic hydrogenation reaction products and intermediates. Among other matters, this can be employed to study the mechanisms of the corresponding chemical transformations. Commonly, noble metal complexes are used for reactions with parahydrogen.
View Article and Find Full Text PDFOrtho-phenylene-bridged phosphinoborane (2,6-Cl Ph) B-C H -PCy 1 was synthesized in three steps from commercially available starting materials. 1 reacts with H or H O under mild conditions to form corresponding zwitterionic phosphonium borates 1-H or 1-H O. NMR studies revealed both reactions to be remarkably reversible.
View Article and Find Full Text PDFWe report nuclear spin hyperpolarization of various alkenes achieved in alkyne hydrogenations with parahydrogen over a metal-free hydroborane catalyst (HCAT). Being an intramolecular frustrated Lewis pair aminoborane, HCAT utilizes a non-pairwise mechanism of H transfer to alkynes that normally prevents parahydrogen-induced polarization (PHIP) from being observed. Nevertheless, the specific spin dynamics in catalytic intermediates leads to the hyperpolarization of predominantly one hydrogen in alkene.
View Article and Find Full Text PDFThe ability of frustrated Lewis pairs (FLPs) to activate H is of significant interest for metal-free catalysis. The activation of H is also the key element of parahydrogen-induced polarization (PHIP), one of the nuclear spin hyperpolarization techniques. It is demonstrated that o-phenylene-based ansa-aminoboranes (AABs) can produce H nuclear spin hyperpolarization through a reversible interaction with parahydrogen at ambient temperatures.
View Article and Find Full Text PDFThe parahydrogen-induced polarization (PHIP) phenomenon, observed when parahydrogen is used in H addition processes, provides a means for substantial NMR signal enhancements and mechanistic studies of chemical reactions. Commonly, noble metal complexes are used for parahydrogen activation, whereas metal-free activation is rare. Herein, we report a series of unimolecular metal-free frustrated Lewis pairs based on an ansa-aminoborane (AAB) moiety in the context of PHIP.
View Article and Find Full Text PDFC-H borylation is a powerful and atom-efficient method for converting affordable and abundant chemicals into versatile organic reagents used in the production of fine chemicals and functional materials. Herein we report a facile C-H borylation of aromatic and olefinic C-H bonds with 2-aminophenylboranes. Computational and experimental studies reveal that the metal-free C-H insertion proceeds via a frustrated Lewis pair mechanism involving heterolytic splitting of the C-H bond by cooperative action of the amine and boryl groups.
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