Gennaro Antonio, Karabanov Alexander, Potapov Alexey, Köckenberger Walter
School of Physics and Astronomy, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
Phys Chem Chem Phys. 2020 Apr 15;22(15):7803-7816. doi: 10.1039/d0cp00892c.
This work explores the dynamic nuclear polarization (DNP) of 1H and 19F nuclei in a sample of 25/75 (% v/v) fluorobenzene/toluene containing the radical 1,3-bisphenylene-2-phenylallyl radical (BDPA) as a polarizing agent. Previously, heteronuclear effects in DNP were studied by analysing the shapes of DNP spectra, or by observing cross-relaxation between nuclei of different types. In this work, we report a rather specific DNP spectrum, where 1H and 19F nuclei obtain polarizations of opposite signs upon microwave (MW) irradiation. In order to explain this observation, we introduce a novel mechanism called heteronuclear thermal mixing (hn-TM). Within this mechanism the spectra of opposite signs can then be explained due to the presence of four-spin systems, involving a pair of dipolar coupled electron spins and hyperfine coupled nuclear spins of 1H and 19F, such that a condition relating their Larmor frequencies |ω1e - ω2e| ≈ ωH - ωF is satisfied. Under this condition, a strong mixing of electron and nuclear states takes place, enabling simultaneous four-spin flip-flops. Irradiation of electron spin transitions with MW followed by such four-spin flip-flops produces non-equilibrium populations of |αHβF and |βHαF states, thus leading to the enhancements of opposite signs for 1H and 19F. Signal enhancements, build-up times and DNP-spectra as a function of MW power and polarizing agent concentration, all provide additional support for assigning the observed DNP mechanism as hn-TM and distinguishing it from other possible mechanisms. We also develop a quantum mechanical model of hn-TM based on averaging of spin Hamiltonians. Simulations based on this model show very good qualitative agreement with experimental data. In addition, the system exhibits cross-relaxation between 1H and 19F induced by the presence of BDPA, which was detected by measuring the 19F signal build-up upon saturation of 1H nuclei with a train of radio-frequency pulses. We demonstrate that such cross-relaxation most likely originates due to the same electron and nuclear states mixing in the four-spin systems.
本工作研究了在含有自由基1,3 - 二亚苯基 - 2 - 苯基烯丙基自由基(BDPA)作为极化剂的25/75(体积比)氟苯/甲苯样品中1H和19F核的动态核极化(DNP)。此前,DNP中的异核效应是通过分析DNP谱的形状或观察不同类型核之间的交叉弛豫来研究的。在本工作中,我们报道了一种相当特殊的DNP谱,其中1H和19F核在微波(MW)辐照下获得相反符号的极化。为了解释这一观察结果,我们引入了一种名为异核热混合(hn - TM)的新机制。在该机制中,由于存在四自旋系统,涉及一对偶极耦合的电子自旋以及1H和19F的超精细耦合核自旋,使得它们的拉莫尔频率满足|ω1e - ω2e| ≈ ωH - ωF的条件,从而可以解释相反符号的谱。在这种条件下,电子和核态发生强烈混合,使得同时发生四自旋翻转。用MW辐照电子自旋跃迁,随后发生这种四自旋翻转,会产生|αHβF和|βHαF态的非平衡布居,从而导致1H和19F的相反符号的增强。信号增强、建立时间以及作为MW功率和极化剂浓度函数的DNP谱,都为将观察到的DNP机制归为hn - TM并将其与其他可能机制区分开来提供了额外支持。我们还基于自旋哈密顿量的平均化开发了hn - TM的量子力学模型。基于该模型的模拟与实验数据显示出非常好的定性一致性。此外,该系统在BDPA存在下表现出1H和19F之间的交叉弛豫,这是通过用一串射频脉冲使1H核饱和后测量19F信号的建立来检测的。我们证明这种交叉弛豫很可能源于四自旋系统中相同的电子和核态混合。