Francis Bitter Magnet Laboratory and Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
J Chem Phys. 2017 Oct 28;147(16):164201. doi: 10.1063/1.5000528.
Dynamic nuclear polarization (DNP) is theoretically able to enhance the signal in nuclear magnetic resonance (NMR) experiments by a factor γ/γ, where γ's are the gyromagnetic ratios of an electron and a nuclear spin. However, DNP enhancements currently achieved in high-field, high-resolution biomolecular magic-angle spinning NMR are well below this limit because the continuous-wave DNP mechanisms employed in these experiments scale as ω where n ∼ 1-2. In pulsed DNP methods, such as nuclear orientation via electron spin-locking (NOVEL), the DNP efficiency is independent of the strength of the main magnetic field. Hence, these methods represent a viable alternative approach for enhancing nuclear signals. At 0.35 T, the NOVEL scheme was demonstrated to be efficient in samples doped with stable radicals, generating H NMR enhancements of ∼430. However, an impediment in the implementation of NOVEL at high fields is the requirement of sufficient microwave power to fulfill the on-resonance matching condition, ω = ω, where ω and ω are the nuclear Larmor and electron Rabi frequencies, respectively. Here, we exploit a generalized matching condition, which states that the effective Rabi frequency, ω, matches ω. By using this generalized off-resonance matching condition, we generate H NMR signal enhancement factors of 266 (∼70% of the on-resonance NOVEL enhancement) with ω/2π = 5 MHz. We investigate experimentally the conditions for optimal transfer of polarization from electrons to H both for the NOVEL mechanism and the solid-effect mechanism and provide a unified theoretical description for these two historically distinct forms of DNP.
动态核极化(DNP)理论上能够通过因子γ/γ增强核磁共振(NMR)实验中的信号,其中γ是电子和核自旋的旋磁比。然而,目前在高场、高分辨率生物分子魔角旋转 NMR 中实现的 DNP 增强远低于这个限制,因为这些实验中采用的连续波 DNP 机制按ω缩放,其中 n ∼ 1-2。在脉冲 DNP 方法中,例如通过电子自旋锁定实现核取向(NOVEL),DNP 效率与主磁场的强度无关。因此,这些方法代表了增强核信号的可行替代方法。在 0.35 T 下,NOVEL 方案在掺杂稳定自由基的样品中被证明是有效的,产生的 H NMR 增强约为 430。然而,在高场中实施 NOVEL 的一个障碍是需要足够的微波功率来满足共振匹配条件,ω = ω,其中 ω 和 ω 分别是核拉莫尔和电子拉比频率。在这里,我们利用广义匹配条件,即有效拉比频率ω匹配ω。通过使用这种广义的非共振匹配条件,我们产生了 H NMR 信号增强因子 266(约为共振 NOVEL 增强的 70%),其中 ω/2π = 5 MHz。我们实验研究了 NOVEL 机制和固态效应机制中从电子向 H 传递极化的最佳条件,并为这两种历史上不同形式的 DNP 提供了统一的理论描述。