In recent years Dynamic Nuclear Polarization (DNP) signal enhancement techniques have become an important and integral part of modern NMR and MRI spectroscopy. The DNP mechanisms transferring polarization from unpaired electrons to the nuclei in the sample is accomplished by microwave (MW) irradiation. For solid samples a distinction is made between three main enhancement processes: Solid Effect (SE), Cross Effect (CE) and Thermal Mixing (TM) DNP. In a recent study we revisited the solid state SE-DNP mechanism at high magnetic fields, using a spin density operator description involving spin relaxation, for the case of an isolated electron spin interacting with neighboring nuclei. In this publication we extend this study by considering the hyper-polarization of nuclei in systems containing two interacting electrons. In these spin systems both processes SE-DNP and CE-DNP are simultaneously active. As previously, a quantum description taking into account spin relaxation is used to calculate the dynamics of spin systems consisting of interacting electron pairs coupled to (core) nuclei. Numerical simulations are used to demonstrate the dependence of the SE- and CE-DNP enhancements on the MW irradiation power and frequency, on electron, nuclear and cross relaxation mechanisms and on the spin interactions. The influence of the presence of many nuclei on the hyper-polarization of an individual core nucleus is examined, showing the similarities between the two DNP processes. These studies also indicate the advantages of the CE- over the SE-DNP processes, both driving the polarization of the bulk nuclei, via the nuclear dipole-dipole interactions.
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http://dx.doi.org/10.1016/j.jmr.2011.09.047 | DOI Listing |
J Am Chem Soc
January 2025
School of Rare Earths, University of Science and Technology of China, Hefei 230026, China.
Achieving ultrahigh permeance and superoleophobicity is crucial for membrane application. Here, we demonstrated that a poly(ionic liquid)/PES hydrogel membrane can achieve dual goals. The high polarity of the ionic liquids induces the water molecules on the membrane surface to be arranged more ordered, as verified by molecular dynamics (MD) simulation and advanced femtosecond sum frequency generation (SFG) vibrational spectroscopy.
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Division of Cancer Biology, Laboratory Animal Center, Fourth Military Medical University, Xi'an, Shaanxi 710032, China.
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View Article and Find Full Text PDFStruct Dyn
January 2025
Center for Free-Electron Laser Science CFEL, Deutsches Elektronen-Synchrotron DESY, Notkestr. 85, 22607 Hamburg, Germany.
Sub-ångström spatial resolution of electron density coupled with sub-femtosecond to few-femtosecond temporal resolution is required to directly observe the dynamics of the electronic structure of a molecule after photoinitiation or some other ultrafast perturbation, such as by soft X-rays. Meeting this challenge, pushing the field of quantum crystallography to attosecond timescales, would bring insights into how the electronic and nuclear degrees of freedom couple, enable the study of quantum coherences involved in molecular dynamics, and ultimately enable these dynamics to be controlled. Here, we propose to reach this realm by employing convergent-beam x-ray crystallography with high-power attosecond pulses from a hard-x-ray free-electron laser.
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December 2024
Community Medicine, Siksha 'O' Anusandhan Deemed to be University Institute of Medical Sciences and SUM Hospital, Bhubaneswar, IND.
Gastric cancer (GC) has become a major challenge in oncology research, primarily due to its detection at advanced stages. In this study, we identified and validated the pharmacological mechanisms involved in treating gastric cancer using an integrated approach combining network pharmacology, molecular docking, and a dynamic approach. Gastric cancer-related genes were obtained from DisGeNET, Genecard, and Malacard databases, while potential targets of bioactive compounds were predicted using SwissTargetPrediction.
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Lemont, Illinois 60439, USA.
Photosynthetic reaction center proteins (RCs) provide ideal model systems for studying quantum entanglement between multiple spins, a quantum mechanical phenomenon wherein the properties of the entangled particles become inherently correlated. Following light-generated sequential electron transfer, RCs generate spin-correlated radical pairs (SCRPs), also referred to as entangled spin qubit (radical) pairs (SQPs). Understanding and controlling coherence mechanisms in SCRP/SQPs is important for realizing practical uses of electron spin qubits in quantum sensing applications.
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