实现极化转移的统一图景--脉冲 DNP 和化学等效的 PHIP

IF 2 3区 化学 Q3 BIOCHEMICAL RESEARCH METHODS
Martin C. Korzeczek , Laurynas Dagys , Christoph Müller , Benedikt Tratzmiller , Alon Salhov , Tim Eichhorn , Jochen Scheuer , Stephan Knecht , Martin B. Plenio , Ilai Schwartz
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引用次数: 0

摘要

核自旋超极化技术,如动态核极化(DNP)和对氢诱导极化(PHIP),给核磁共振和磁共振成像带来了革命性的变化。在这些方法中,现成的高自旋阶数源(DNP 中的电子自旋或 PHIP 中的氢单态)被带到核自旋目标附近,从而在外部量子控制下实现自旋阶数的有效转移。尽管 DNP 中的电子自旋和 PHIP 中的核单子态在能量尺度和相互作用机制上存在巨大差异,但伪自旋形式主义使我们能够建立一种有趣的等价关系。因此,PHIP 的重要低场极化转移机制可以映射到与脉冲 DNP 相当的类似系统上。这就在 PHIP 和 DNP 的关键极化转移序列之间建立了对应关系,促进了序列发展概念的转移。这将为 DNP 和 PHIP 偏振序列开发人员提供新的见解和重要的交叉交流机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Towards a unified picture of polarization transfer — pulsed DNP and chemically equivalent PHIP

Towards a unified picture of polarization transfer — pulsed DNP and chemically equivalent PHIP

Nuclear spin hyperpolarization techniques, such as dynamic nuclear polarization (DNP) and parahydrogen-induced polarization (PHIP), have revolutionized nuclear magnetic resonance and magnetic resonance imaging. In these methods, a readily available source of high spin order, either electron spins in DNP or singlet states in hydrogen for PHIP, is brought into close proximity with nuclear spin targets, enabling efficient transfer of spin order under external quantum control. Despite vast disparities in energy scales and interaction mechanisms between electron spins in DNP and nuclear singlet states in PHIP, a pseudo-spin formalism allows us to establish an intriguing equivalence. As a result, the important low-field polarization transfer regime of PHIP can be mapped onto an analogous system equivalent to pulsed-DNP. This establishes a correspondence between key polarization transfer sequences in PHIP and DNP, facilitating the transfer of sequence development concepts. This promises fresh insights and significant cross-pollination between DNP and PHIP polarization sequence developers.

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来源期刊
CiteScore
3.80
自引率
13.60%
发文量
150
审稿时长
69 days
期刊介绍: The Journal of Magnetic Resonance presents original technical and scientific papers in all aspects of magnetic resonance, including nuclear magnetic resonance spectroscopy (NMR) of solids and liquids, electron spin/paramagnetic resonance (EPR), in vivo magnetic resonance imaging (MRI) and spectroscopy (MRS), nuclear quadrupole resonance (NQR) and magnetic resonance phenomena at nearly zero fields or in combination with optics. The Journal''s main aims include deepening the physical principles underlying all these spectroscopies, publishing significant theoretical and experimental results leading to spectral and spatial progress in these areas, and opening new MR-based applications in chemistry, biology and medicine. The Journal also seeks descriptions of novel apparatuses, new experimental protocols, and new procedures of data analysis and interpretation - including computational and quantum-mechanical methods - capable of advancing MR spectroscopy and imaging.
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