Hyperpolarization of [13C]formate using parahydrogen

IF 2.624
Dudari B. Burueva , Sergey V. Sviyazov , Nikita V. Chukanov , Nazim R. Mustafin , Oleg G. Salnikov , Eduard Y. Chekmenev , Kirill V. Kovtunov , Igor V. Koptyug
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引用次数: 0

Abstract

Sodium [13C]formate was successfully hyperpolarized using parahydrogen-induced polarization by means of side-arm hydrogenation (PHIP-SAH). Allyl [13C]formate was hyperpolarized using homogeneous hydrogenation of the corresponding unsaturated precursor (propargyl [13C]formate) in acetone-d6 with parahydrogen. The observed proton polarization was estimated as 16.6 ± 0.6 % while achieving 80 % chemical conversion. The 1H-to-13C polarization transfer was performed using magnetic field cycling. The highest observed polarization for 13C nuclei was estimated as 1.7 ± 0.2 % and was obtained at 250 nT polarization transfer magnetic field. We demonstrate that the 13C hyperpolarization is retained during the hydrolysis of allyl [13C]formate and hyperpolarized sodium [13C]formate was produced with P13C of 0.4 ± 0.1 %.

Abstract Image

使用对氢使[13C]甲酸盐超极化
通过侧臂氢化(PHIP-SAH)方法,利用对氢诱导极化成功地使[13C]甲酸钠超极化。在丙酮-d6 中,利用对氢对相应的不饱和前体([13C]甲酸丙炔酯)进行均相氢化,使[13C]甲酸烯丙酯超极化。观察到的质子极化估计为 16.6 ± 0.6 %,化学转化率达到 80%。从 1H 到 13C 的极化转移是通过磁场循环进行的。在 250 nT 的极化转移磁场中,13C 核的最高极化观测值估计为 1.7 ± 0.2 %。我们证明,在烯丙基[13C]甲酸酯水解过程中,13C 超极化被保留下来,并产生了超极化的[13C]甲酸钠,其 P13C 为 0.4 ± 0.1 %。
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CiteScore
1.90
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