Heteronuclear DNP of 1H and 19F nuclei using BDPA as a polarizing agent
文献信息
Antonio Gennaro, Alexander Karabanov, Alexey Potapov, Walter Köckenberger
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.
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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.


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