Aqueous ligand-stabilized palladium nanoparticle catalysts for parahydrogen 
induced13C hyperpolarization.

McCormick, J.; Grunfeld, A. M.; Ertas, Y. N.; Biswas, A. N.; Marsh, K. L.; Wagner, S,; Glöggler, S.; Bouchard, L. S.

doi:10.1021/acs.analchem.7b01363

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Aqueous ligand-stabilized palladium nanoparticle catalysts for parahydrogen induced ¹³C hyperpolarization.

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Glöggler, S.
Research Group of NMR Signal Enhancement, MPI for Biophysical Chemistry, Max Planck Society;

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Citation

McCormick, J., Grunfeld, A. M., Ertas, Y. N., Biswas, A. N., Marsh, K. L., Wagner, S., et al. (2017). Aqueous ligand-stabilized palladium nanoparticle catalysts for parahydrogen induced ¹³C hyperpolarization. Analytical Chemistry, 89(13), 7190-7194. doi:10.1021/acs.analchem.7b01363.

Cite as: https://hdl.handle.net/11858/00-001M-0000-002D-6109-D

Abstract

Parahydrogen induced polarization (PHIP) is a method for enhancing NMR sensitivity. The pairwise addition of parahydrogen in aqueous medium by heterogeneous catalysts can lead to applications in chemical and biological systems. Polarization enhancement can be transferred from 1H to 13C for longer lifetimes by use of zero field cycling. In this work, water-dispersible N-acetylcysteine- and L-cysteine-stabilized palladium nanoparticles are introduced and carbon polarizations up to two orders of magnitude higher than previous aqueous heterogeneous PHIP systems are presented. P13C values of 1.2% and 0.2% are achieved for the formation of hydroxyethyl propionate from hydroxyethyl acrylate and ethyl acetate from vinyl acetate, respectively. Both nanoparticle systems are easily synthesized in open air, and TEM indicates an average size of 2.4 ± 0.6 nm for NAC@Pd and 2.5 ± 0.8 nm for LCys@Pd nanoparticles with 40% and 25% ligand coverage determined by thermogravimetric analysis, respectively. As a step toward biological relevance, results are presented for the unprotected amino acid allylglycine upon aqueous hydrogenation of propargylglycine.