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Optically Enhanced Solid-State 1 H NMR Spectroscopy.

Authors :
De Biasi F
Hope MA
Avalos CE
Karthikeyan G
Casano G
Mishra A
Badoni S
Stevanato G
Kubicki DJ
Milani J
Ansermet JP
Rossini AJ
Lelli M
Ouari O
Emsley L
Source :
Journal of the American Chemical Society [J Am Chem Soc] 2023 Jul 12; Vol. 145 (27), pp. 14874-14883. Date of Electronic Publication: 2023 Jun 27.
Publication Year :
2023

Abstract

Low sensitivity is the primary limitation to extending nuclear magnetic resonance (NMR) techniques to more advanced chemical and structural studies. Photochemically induced dynamic nuclear polarization (photo-CIDNP) is an NMR hyperpolarization technique where light is used to excite a suitable donor-acceptor system, creating a spin-correlated radical pair whose evolution drives nuclear hyperpolarization. Systems that exhibit photo-CIDNP in solids are not common, and this effect has, up to now, only been observed for <superscript>13</superscript> C and <superscript>15</superscript> N nuclei. However, the low gyromagnetic ratio and natural abundance of these nuclei trap the local hyperpolarization in the vicinity of the chromophore and limit the utility for bulk hyperpolarization. Here, we report the first example of optically enhanced solid-state <superscript>1</superscript> H NMR spectroscopy in the high-field regime. This is achieved via photo-CIDNP of a donor-chromophore-acceptor molecule in a frozen solution at 0.3 T and 85 K, where spontaneous spin diffusion among the abundant strongly coupled <superscript>1</superscript> H nuclei relays polarization through the whole sample, yielding a 16-fold bulk <superscript>1</superscript> H signal enhancement under continuous laser irradiation at 450 nm. These findings enable a new strategy for hyperpolarized NMR beyond the current limits of conventional microwave-driven DNP.

Details

Language :
English
ISSN :
1520-5126
Volume :
145
Issue :
27
Database :
MEDLINE
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
37366803
Full Text :
https://doi.org/10.1021/jacs.3c03937