Toward production of pure 13C hyperpolarized metabolites using heterogeneous parahydrogen-induced polarization of ethyl[1-13C]acetate

被引:0
|
作者
Kovtunov, K. V. [1 ,2 ]
Barskiy, D. A. [3 ]
Salnikov, O. G. [1 ,2 ]
Shchepin, R. V. [3 ]
Coffey, A. M. [3 ]
Kovtunova, L. M. [2 ,4 ]
Bukhtiyarov, V. I. [2 ,4 ]
Koptyug, I. V. [1 ,2 ]
Chekmenev, E. Y. [3 ,5 ]
机构
[1] Int Tomog Ctr SB RAS, Lab Magnet Resonance Microimaging, Inst Skaya St 3A, Novosibirsk 630090, Russia
[2] Novosibirsk State Univ, Pirogova St 2, Novosibirsk 630090, Russia
[3] Vanderbilt Univ, Inst Imaging Sci VUIIS, Dept Radiol, Dept Biomed Engn,VICC, Nashville, TN 37232 USA
[4] SB RAS, Boreskov Inst Catalysis, 5 Acad Lavrentiev Pr, Novosibirsk 630090, Russia
[5] Russian Acad Sci, Leninskiy Prospect 14, Moscow 119991, Russia
来源
RSC ADVANCES | 2016年 / 6卷 / 74期
基金
俄罗斯科学基金会; 美国国家科学基金会;
关键词
HYDROGEN-INDUCED POLARIZATION; NMR SIGNAL ENHANCEMENT; IN-VIVO; MAGNETIC-RESONANCE; PASADENA HYPERPOLARIZATION; AQUEOUS-PHASE; CATALYST; EXCHANGE; PYRUVATE; WATER;
D O I
10.1039/c6ra15808k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here, we report the production of C-13-hyperpolarized ethyl acetate via heterogeneously catalyzed pairwise addition of parahydrogen to vinyl acetate over TiO2-supported rhodium nanoparticles, followed by magnetic field cycling. Importantly, the hyperpolarization is demonstrated even at the natural abundance of C-13 isotope (ca. 1.1%) along with the easiest separation of the catalyst from the hyperpolarized liquid.
引用
收藏
页码:69728 / 69732
页数:5
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