Dynamic Nuclear Polarization of Long-Lived Nuclear Spin States in Methyl Groups

被引:27
|
作者
Dumez, Jean-Nicolas [1 ]
Vuichoud, Basile [2 ,3 ]
Mammoli, Daniele [2 ]
Bornet, Aurelien [2 ,3 ]
Pinon, Arthur C. [2 ]
Stevanato, Gabriele [2 ]
Meier, Benno [4 ]
Bodenhausen, Geoffrey [5 ]
Jannin, Sami [2 ,3 ]
Levitt, Malcolm H. [4 ]
机构
[1] Univ Paris Saclay, Univ Paris Sud, CNRS UPR2301, Inst Chim Subst Nat, F-91190 Gif Sur Yvette, France
[2] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
[3] Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, ENS Lyon,Inst Sci Analyt,UMR 5280, F-69100 Villeurbanne, France
[4] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[5] UPMC, ENS, CNRS, Lab Biomol,UMR7203, F-75005 Paris, France
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2017年 / 8卷 / 15期
基金
欧洲研究理事会; 英国工程与自然科学研究理事会; 瑞士国家科学基金会;
关键词
SOLID-STATE; THEORETICAL ASPECTS; PARA-HYDROGEN; SINGLET ORDER; TEMPERATURE;
D O I
10.1021/acs.jpclett.7b01512
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have induced hyperpolarized long-lived states in compounds containing C-13-bearing methyl groups by dynamic nuclear polarization (DNP) at cryogenic temperatures, followed by dissolution with a warm solvent. The hyper polarized methyl long-lived states give rise to enhanced antiphase C-13 NMR signals in solution, which often persist for times much longer than the C-13 and H-1 spin-lattice relaxation times under the same conditions. The DNP-induced effects are similar to quantum-rotor-induced polarization (QRIP) but are observed in a wider range of compounds because they do not depend critically on the height of the rotational barrier. We interpret our observations with a model in which nuclear Zeeman and methyl tunnelling reservoirs adopt an approximately uniform temperature, under DNP conditions. The generation of hyperpolarized NMR signals that persist for relatively long times in a range of methyl-bearing substances may be important for applications such as investigations of metabolism, enzymatic reactions, protein ligand binding, drug screening, and molecular imaging.
引用
收藏
页码:3549 / 3555
页数:7
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