1 H‐decoupling and Isotopic Labeling for the Measurement of the Longitudinal Relaxation Time of Hyperpolarized 13 C‐Methylenes in Choline Analogs
1 H‐decoupling and Isotopic Labeling for the Measurement of the Longitudinal Relaxation Time of Hyperpolarized 13 C‐Methylenes in Choline Analogs
复制标题
1 H-解偶联和同位素标记用于测量胆碱类似物中超极化 13 C-亚甲基的纵向弛豫时间
DOI:
10.1002/ijch.201900016
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发表时间:
2019
影响因子:
3.2
通讯作者:
Katz‐Brull, Rachel
中科院分区:
文献类型:
--
作者:
Uppala, Sivaranjan;Gamliel, Ayelet;Harris, Talia;Sosna, Jacob;Gomori, J. Moshe;Jerschow, Alexej;Katz‐Brull, Rachel
The T1of a hyperpolarized site in solution is a key parameter that determines the time‐window in which its NMR signals are observable. For13C sites adjacent to protons,1H‐decoupling has been shown to increase the hyperpolarized signal resolution and SNR. Additionally, polarization transfer to protons has shown utility in increasing the sensitivity of detection. However,1H‐decoupling could lead to a change in the decay rate of a hyperpolarized13C site. Here we tested this possible effect in a case where the protons are directly bound to an sp3hyperpolarized13C site (using [1,2‐13C2]choline) and1H‐decoupling was applied continuously throughout the hyperpolarized decay measurement. We found that1H‐decoupling did not lead to any significant changes in the13C polarization decay time but did result in the expected collapse of J‐coupling and produced sharper signals. This result suggested that1H‐decoupling did not affect the decay rate of hyperpolarized sp3 13C sites. The deuterium‐substitution approach (using [1,1,2,2‐D4,1‐13C]choline) showed a dramatic prolongation of T1. Upper bounds on the T1of all investigated sites were calculated.