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Title

Through-bond and through-space radiofrequency amplification by stimulated emission of radiation.

Authors

Trofimov, Ivan A.; Salnikov, Oleg G.; Pravdivtsev, Andrey N.; de Maissin, Henri; Yi, Anna P.; Chekmenev, Eduard Y.; Hövener, Jan-Bernd; Schmidt, Andreas B.; Koptyug, Igor V.

Abstract

Radio Amplification by Stimulated Emission of Radiation (RASER) is a phenomenon observed during nuclear magnetic resonance (NMR) experiments with strongly negatively polarized systems. This phenomenon may be utilized for the production of very narrow NMR lines, background-free NMR spectroscopy, and excitation-free sensing of chemical transformations. Recently, novel methods of producing RASER by ParaHydrogen-Induced Polarization (PHIP) were introduced. Here, we show that pairwise addition of parahydrogen to various propargylic compounds induces RASER activity of other protons beyond those chemically introduced in the reaction. In high-field PHIP, negative polarization initiating RASER is transferred via intramolecular cross-relaxation. When parahydrogen is added in Earth's field followed by adiabatic transfer to a high field, RASER activity of other protons is induced via both J-couplings and cross-relaxation. This through-bond and through-space induction of RASER holds potential for the ongoing development and expansion of RASER applications and can potentially enhance spectral resolution in two-dimensional NMR spectroscopy techniques. Radio Amplification by Stimulated Emission of Radiation (RASER) may produce very narrow NMR lines, background-free NMR spectroscopy, and excitation-free sensing of chemical transformations. Here, the authors show that pairwise addition of parahydrogen to various propargylic compounds induces RASER activity of other protons beyond those chemically introduced in the reaction via through-bond or through-space interactions.

Subjects

STIMULATED emission; NUCLEAR magnetic resonance; CHEMICAL amplification; PARAHYDROGEN; RADIATION

Publication

Communications Chemistry, 2024, Vol 7, Issue 1, p1

ISSN

2399-3669

Publication type

Academic Journal

DOI

10.1038/s42004-024-01313-0

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